b-CD dimers Py1-Py4 bearing 2,2'-bipyridine-4,4'-dicarboxy tether der. 3
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
None None VD-0258 None

SMILES:

Supramolecules

Namelog KSDpHT(°C)MethodRef
[b-CD dimers Py1-Py4 bearing 2,2'-bipyridine-4,4'-dicarboxy tether der. 3](1).[sodium cholate] 4.09 2.48 7.4 25.0 Isothermal titration calorimetry Yu Liu 2005
[b-CD dimers Py1-Py4 bearing 2,2'-bipyridine-4,4'-dicarboxy tether der. 3](1).[sodium deoxycholate] 4.09 2.30 7.4 25.0 Isothermal titration calorimetry Yu Liu 2005

b-CD dimers Py1-Py4 bearing 2,2'-bipyridine-4,4'-dicarboxy tether der. 4
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
None None VD-0259 None

SMILES:

Supramolecules

Namelog KSDpHT(°C)MethodRef
[b-CD dimers Py1-Py4 bearing 2,2'-bipyridine-4,4'-dicarboxy tether der. 4](1).[sodium cholate] 3.83 2.30 7.4 25.0 Isothermal titration calorimetry Yu Liu 2005
[b-CD dimers Py1-Py4 bearing 2,2'-bipyridine-4,4'-dicarboxy tether der. 4](1).[sodium deoxycholate] 4.12 2.60 7.4 25.0 Isothermal titration calorimetry Yu Liu 2005

b-CD dimers Se1-Se4 bearing 2,2'-diselenobis(benzoyl) tether der. SE3
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
None None VD-0152 None

SMILES:

Supramolecules

Namelog KSDpHT(°C)MethodRef
[b-CD dimers Se1-Se4 bearing 2,2'-diselenobis(benzoyl) tether der. SE3](1).[sodium cholate] 3.61 2.30 7.4 25.0 Isothermal titration calorimetry Yu Liu 2005
[b-CD dimers Se1-Se4 bearing 2,2'-diselenobis(benzoyl) tether der. SE3](1).[sodium deoxycholate] 3.73 2.30 7.4 25.0 Isothermal titration calorimetry Yu Liu 2005

b-CD dimers Se1-Se4 bearing 2,2'-diselenobis(benzoyl) tether der. SE4
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
None None VD-0153 None

SMILES:

Supramolecules

Namelog KSDpHT(°C)MethodRef
[b-CD dimers Se1-Se4 bearing 2,2'-diselenobis(benzoyl) tether der. SE4](1).[sodium cholate] 3.70 1.30 7.4 25.0 Isothermal titration calorimetry Yu Liu 2005
[b-CD dimers Se1-Se4 bearing 2,2'-diselenobis(benzoyl) tether der. SE4](1).[sodium deoxycholate] 3.79 1.30 7.4 25.0 Isothermal titration calorimetry Yu Liu 2005

b-CD-peptide
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
None None VD-0326 None

SMILES:

Supramolecules

Namelog KSDpHT(°C)MethodRef
[b-CD-peptide](1).[Lithocholic acid] 5.64 4.23 7.5 25.0 Fluorescence resonance energy transfer Hisakazu Mihara 2003
[b-CD-peptide](1).[Hyodeoxycholic acid] 5.32 3.79 7.5 25.0 Fluorescence resonance energy transfer Hisakazu Mihara 2003
[b-CD-peptide](1).[Ursodeoxycholic acid] 5.24 3.61 7.5 25.0 Fluorescence resonance energy transfer Hisakazu Mihara 2003
[b-CD-peptide](1).[Chenodeoxycholic acide] 4.52 2.90 7.5 25.0 Fluorescence resonance energy transfer Hisakazu Mihara 2003
[b-CD-peptide](1).[Deoxycholic acid] 3.04 1.95 7.5 25.0 Fluorescence resonance energy transfer Hisakazu Mihara 2003
[b-CD-peptide](1).[Cholic acid] 2.95 2.66 7.5 25.0 Fluorescence resonance energy transfer Hisakazu Mihara 2003

b-CDN+ copolymer
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
None None VD-0009 None

SMILES:

Supramolecules

Namelog KSDpHT(°C)MethodRef
[b-CDN+ copolymer](1).[N-(1,1-dimethylethyl)-4-hydroxybenzene-1,2-dicarboximide] 3.47 2.5 25.0 Fluorescence spectroscopy Noelle Martine Gosselet 2005
[b-CDN+ copolymer](1).[N-(1,1-dimethylethyl)-4-aminobenzene-1,2-dicarboximide] 3.42 7.0 25.0 Fluorescence spectroscopy Noelle Martine Gosselet 2005
[b-CDN+ copolymer](1).[DM17] 1.70 2.5 25.0 Fluorescence spectroscopy Noelle Martine Gosselet 2005
[b-CDN+ copolymer](1).[DM17] 2.20 7.0 25.0 Fluorescence spectroscopy Noelle Martine Gosselet 2005

b-Cyclodextrin
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
None None CY-2001 None

SMILES:

Supramolecules

Namelog KSDpHT(°C)MethodRef
[b-Cyclodextrin](1).[1-anilinonaphthalene-8-sulfonate] 1.93 25.0 Fluorometric method PARK, J.W., 1989
[b-Cyclodextrin](1).[2-anilino-7-naphthalenesulfonate] 3.18 25.0 Fluorometric method PARK, J.W., 1989
[b-Cyclodextrin](1).[Fluorescein] 2.56 Induced circular dichroism absorption spectroscopy and steady-state and picosecond time resolved fluorescence spectroscopy Flamigni, Lucia 1993
[b-Cyclodextrin](1).[Fluorescein] 3.08 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Erythrosine B] 1.60 Induced circular dichroism absorption spectroscopy and steady-state and picosecond time resolved fluorescence spectroscopy Flamigni, Lucia 1993
[b-Cyclodextrin](1).[Rhodamine B] 3.46 Flamigni, Lucia 1993
[b-Cyclodextrin](1).[Rhodamine B] 3.77 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Rhodamine B] 3.63 7.2 25.0 Fluorescence spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[N-adamantan-1'-ylpyrazinium cation] 3.49 6.8 25.0 1H NMR chemical shift titration and visible spectrophotometric titration Donald H. Macartney 1993
[b-Cyclodextrin](1).[(N-adamantan-1'-ylpyrazinium)pentacyanoferrate (II)-ion] 3.20 6.8 25.0 1H NMR chemical shift titration and visible spectrophotometric titration Donald H. Macartney 1993
[b-Cyclodextrin](1).[Dodecyltrimethylammonium bromide] 4.25 0.03 25.0 Potenciometric method Turmine, M 1995
[b-Cyclodextrin](1).[6-(p-toluidino)-2-naphtalene-6-sulfonate] 3.39 3.5 fluorometric titration Sakairi, Nobuo 1996
[b-Cyclodextrin](1).[6-(p-toluidino)-2-naphtalene-6-sulfonate] 3.42 5.2 fluorometric titration Sakairi, Nobuo 1996
[b-Cyclodextrin](1).[6-(p-toluidino)-2-naphtalene-6-sulfonate] 3.40 7.0 fluorometric titration Sakairi, Nobuo 1996
[b-Cyclodextrin](1).[6-(p-toluidino)-2-naphtalene-6-sulfonate] 3.43 8.3 fluorometric titration Sakairi, Nobuo 1996
[b-Cyclodextrin](1).[6-(p-toluidino)-2-naphtalene-6-sulfonate] 3.42 11.0 fluorometric titration Sakairi, Nobuo 1996
[b-Cyclodextrin](1).[6-(p-toluidino)-2-naphtalene-6-sulfonate] 3.27 1.00 7.0 25.0 fluorescence spectroscopy Lincoln, Stephen F. 1996
[b-Cyclodextrin](1).[2-(p-aminophenyl)-3,3-dimethyl-5-carboethoxy-3H-indole] 2.92 2.11 9.5 Steady-state fluorescence Durocher, Gilles 1997
[b-Cyclodextrin](2).[2-(p-aminophenyl)-3,3-dimethyl-5-carboethoxy-3H-indole] 3.42 2.32 9.5 Steady-state fluorescence Durocher, Gilles 1997
[b-Cyclodextrin](1).[2-(p-dimethylaminophenyl)-3,3-dimethyl-5-carboethoxy-3H-indole] 3.25 2.54 9.5 Steady-state fluorescence Durocher, Gilles 1997
[b-Cyclodextrin](2).[2-(p-dimethylaminophenyl)-3,3-dimethyl-5-carboethoxy-3H-indole] 3.71 2.66 9.5 Steady-state fluorescence Durocher, Gilles 1997
[b-Cyclodextrin](1).[2-(p-aminophenyl)-3,3-dimethyl-5-cyano-3H-indole] 2.88 2.08 9.5 Steady-state fluorescence Durocher, Gilles 1997
[b-Cyclodextrin](2).[2-(p-aminophenyl)-3,3-dimethyl-5-cyano-3H-indole] 2.88 1.78 9.5 Steady-state fluorescence Durocher, Gilles 1997
[b-Cyclodextrin](1).[2-(p-dimethylaminophenyl)-3,3-dimethyl-5-cyano-3H-indole] 3.16 2.34 9.5 Steady-state fluorescence Durocher, Gilles 1997
[b-Cyclodextrin](2).[2-(p-dimethylaminophenyl)-3,3-dimethyl-5-cyano-3H-indole] 3.27 2.18 9.5 Steady-state fluorescence Durocher, Gilles 1997
[b-Cyclodextrin](1).[Nicotin] 1.34 1.08 25.0 Capillary electrophoresis Berglund, Johan 1997
[b-Cyclodextrin](1).[Nicotin] 1.34 1.08 37.0 Capillary electrophoresis Berglund, Johan 1997
[b-Cyclodextrin](1).[Nicotin] 2.55 10.0 Capillary electrophoresis Berglund, Johan 1997
[b-Cyclodextrin](1).[Nicotin] 2.38 10.0 25.0 Capillary electrophoresis Berglund, Johan 1997
[b-Cyclodextrin](1).[2-(p-methylaminophenyl)-3,3-dimethyl-5-carboethoxy-3H-indole] 3.14 2.45 9.5 Steady-state fluorescence Durocher, Gilles 1997
[b-Cyclodextrin](2).[2-(p-methylaminophenyl)-3,3-dimethyl-5-carboethoxy-3H-indole] 3.51 2.41 9.5 Steady-state fluorescence Durocher, Gilles 1997
[b-Cyclodextrin](1).[(2,3,7-triamino-6-phenil-pteridine)] 2.53 20.0 phase solubility Arias, M. J. 1997
[b-Cyclodextrin](1).[(2,3,7-triamino-6-phenil-pteridine)] 2.67 20.0 spectral shift Arias, M. J. 1997
[b-Cyclodextrin](1).[carbaryl] 2.46 1.32 25.0 phase solubility La Rotonda, Maria Immacolata 2000
[b-Cyclodextrin](1).[procaine hydrochloride] 2.63 15.0 Steady-state fluorescence Aicart, E. 2000
[b-Cyclodextrin](1).[procaine hydrochloride] 2.57 20.0 Steady-state fluorescence Aicart, E. 2000
[b-Cyclodextrin](1).[procaine hydrochloride] 2.52 25.0 Steady-state fluorescence Aicart, E. 2000
[b-Cyclodextrin](1).[procaine hydrochloride] 2.45 30.0 Steady-state fluorescence Aicart, E. 2000
[b-Cyclodextrin](1).[procaine hydrochloride] 2.40 35.0 Steady-state fluorescence Aicart, E. 2000
[b-Cyclodextrin](1).[procaine hydrochloride] 2.33 40.0 Steady-state fluorescence Aicart, E. 2000
[b-Cyclodextrin](1).[procaine hydrochloride] 2.47 15.0 UV-vis measurements Aicart, E. 2000
[b-Cyclodextrin](1).[procaine hydrochloride] 2.31 25.0 UV-vis measurements Aicart, E. 2000
[b-Cyclodextrin](1).[procaine hydrochloride] 2.18 40.0 UV-vis measurements Aicart, E. 2000
[b-Cyclodextrin](1).[procaine hydrochloride] 0.14 Constant current coulometric titration (CCCT) Jinghao Pan 1999
[b-Cyclodextrin](1).[procaine hydrochloride] 0.00 Fluorescence spectroscopy Jinghao Pan 1999
[b-Cyclodextrin](1).[imipramine] 3.17 2.18 25.0 conductivity measurments Aicart, E. 2001
[b-Cyclodextrin](1).[desipramine] 3.31 2.30 25.0 conductivity measurments Aicart, E. 2001
[b-Cyclodextrin](1).[amitriptyline] 3.50 2.48 25.0 conductivity measurments Aicart, E. 2001
[b-Cyclodextrin](1).[5-benzoyl-1H-benzimidazol-2-yl-carbamic acide methyl ester] 3.29 7.2 15.0 Higuchi and Connors solubility method Shehatta, Ibrahim 2002
[b-Cyclodextrin](1).[5-benzoyl-1H-benzimidazol-2-yl-carbamic acide methyl ester] 3.21 7.2 20.0 Higuchi and Connors solubility method Shehatta, Ibrahim 2002
[b-Cyclodextrin](1).[5-benzoyl-1H-benzimidazol-2-yl-carbamic acide methyl ester] 3.14 7.2 25.0 Higuchi and Connors solubility method Shehatta, Ibrahim 2002
[b-Cyclodextrin](1).[5-benzoyl-1H-benzimidazol-2-yl-carbamic acide methyl ester] 3.18 7.5 25.0 Higuchi and Connors solubility method Shehatta, Ibrahim 2002
[b-Cyclodextrin](1).[5-benzoyl-1H-benzimidazol-2-yl-carbamic acide methyl ester] 3.07 7.2 30.0 Higuchi and Connors solubility method Shehatta, Ibrahim 2002
[b-Cyclodextrin](1).[5-benzoyl-1H-benzimidazol-2-yl-carbamic acide methyl ester] 2.95 7.2 40.0 Higuchi and Connors solubility method Shehatta, Ibrahim 2002
[b-Cyclodextrin].[phenol] 2.33 25.0 near-infrared spectrometry Tran, Chieu D. 2002
[b-Cyclodextrin](2).[(-)-a-bisabolol] 2.44 20.0 phase solubility Schmidt, P. C. 2003
[b-Cyclodextrin](2).[D-limonene] 2.43 20.0 phase solubility Schmidt, P. C. 2003
[b-Cyclodextrin](2).[1,8-cineole] 2.29 20.0 phase solubility Schmidt, P. C. 2003
[b-Cyclodextrin](1).[7-methoxycoumarin] 2.11 1.51 fluorescence suppression Wagner, Brian D. 2003
[b-Cyclodextrin](1).[1-b-D ribofuranosyl-1-H-1,2,4-triazole-3-carboxamide] 3.42 4.6 18.0 HPLC Kedzierewicz, F. 2005
[b-Cyclodextrin](1).[allopurinol] 1.20 6.5 25.0 NMR diffusion measurements Jimenez, V Alderete 2006
[b-Cyclodextrin](1).[allopurinol] 1.48 10.0 25.0 NMR diffusion measurements Jimenez, V Alderete 2006
[b-Cyclodextrin](1).[indol] 2.37 7.2 15.0 absorption and fluorescence spectroscopy J. B. Alexander Ross 1987
[b-Cyclodextrin](1).[indol] 2.38 7.2 15.8 absorption and fluorescence spectroscopy J. B. Alexander Ross 1987
[b-Cyclodextrin](1).[indol] 2.26 7.2 25.0 absorption and fluorescence spectroscopy J. B. Alexander Ross 1987
[b-Cyclodextrin](1).[indol] 2.23 7.2 30.0 absorption and fluorescence spectroscopy J. B. Alexander Ross 1987
[b-Cyclodextrin](1).[indol] 2.15 7.2 37.2 absorption and fluorescence spectroscopy J. B. Alexander Ross 1987
[b-Cyclodextrin](1).[indol] 2.29 7.2 25.0 absorption J. B. Alexander Ross 1987
[b-Cyclodextrin](1).[indol] 2.26 7.2 25.0 fluorescence spectroscopy J. B. Alexander Ross 1987
[b-Cyclodextrin](1).[C14 acid] 3.77 0.05 8.2 30.0 capillar zone electrophoresis P. Gareil 1995
[b-Cyclodextrin](1).[C13 acid] 3.58 0.05 8.2 30.0 capillar zone electrophoresis P. Gareil 1995
[b-Cyclodextrin](1).[C12 acid] 3.13 0.05 8.2 30.0 capillar zone electrophoresis P. Gareil 1995
[b-Cyclodextrin](1).[C11 acid] 2.60 0.10 8.2 30.0 capillar zone electrophoresis P. Gareil 1995
[b-Cyclodextrin](1).[C10 acid] 2.20 0.20 8.2 30.0 capillar zone electrophoresis P. Gareil 1995
[b-Cyclodextrin](1).[C9 acid] 1.90 0.30 8.2 30.0 capillar zone electrophoresis P. Gareil 1995
[b-Cyclodextrin](1).[oxazepam] 2.31 phase solubility Moyano, J. R. 1995
[b-Cyclodextrin](1).[oxazepam] 2.70 spectral shift method Moyano, J. R. 1995
[b-Cyclodextrin](1).[N-(3,5-dinitrobenzoyl)-L-homophenylalanine] 2.67 0.95 6.5 22.0 capillar zone electrophoresis Apryll M. Stalcup 1995
[b-Cyclodextrin](1).[N-(3,5-dinitrobenzoyl)-D-homophenylalanine] 2.66 1.00 6.5 22.0 capillar zone electrophoresis Apryll M. Stalcup 1995
[b-Cyclodextrin](1).[N-(3,5-dinitrobenzoyl)-L-phenylglycine] 2.41 0.60 6.5 22.0 capillar zone electrophoresis Apryll M. Stalcup 1995
[b-Cyclodextrin](1).[N-(3,5-dinitrobenzoyl)-D-phenylglycine] 2.21 0.48 6.5 22.0 capillar zone electrophoresis Apryll M. Stalcup 1995
[b-Cyclodextrin](1).[N-(3,5-dinitrobenzoyl)phenylalanin] 1.63 0.60 6.5 22.0 capillar zone electrophoresis Apryll M. Stalcup 1995
[b-Cyclodextrin](2).[6-(p-toluidino)-2-naphtalene-6-sulfonate] 1.93 0.70 7.0 25.0 fluorescence spectroscopy Lincoln, Stephen F. 1996
[b-Cyclodextrin](1).[dimethyl-phthalate] 1.60 25.0 fluorescence spectroscopy Murai, Shoji 1998
[b-Cyclodextrin](1).[diethyl-phthalate] 2.42 25.0 fluorescence spectroscopy Murai, Shoji 1998
[b-Cyclodextrin](1).[dipropyl-phthalate] 3.31 25.0 fluorescence spectroscopy Murai, Shoji 1998
[b-Cyclodextrin](1).[dibutyl-phthalate] 4.50 25.0 fluorescence spectroscopy Murai, Shoji 1998
[b-Cyclodextrin](1).[diheptyl-phthalate] 6.95 25.0 fluorescence spectroscopy Murai, Shoji 1998
[b-Cyclodextrin](1).[di(2-ethylhexyl)-phthalate] 7.54 25.0 fluorescence spectroscopy Murai, Shoji 1998
[b-Cyclodextrin].[11-(ferrocenylcarbonyloxy)undecanethiol] 4.56 3.60 6.0 20.0 cyclic voltammetric Leech, Donal 1998
[b-Cyclodextrin](1).[L-tryptophan] 3.26 0.04 7.2 25.0 Calorimetry Yu Liu 1998
[b-Cyclodextrin](1).[L-tryptophan] 2.61 2.39 8.0 18.0 UV-vis spectroscopy Andrzej Temeriusz 2006
[b-Cyclodextrin](1).[Sodium 3-hydroxy-2-naphthoate] 2.15 0.02 7.2 25.0 Calorimetry Yu Liu 1998
[b-Cyclodextrin](1).[Disodium 2,7-naphthalenedisulfonate] 2.44 0.02 7.2 25.0 Calorimetry Yu Liu 1998
[b-Cyclodextrin](1).[sodium 2-naphthalenesulfonate] 5.37 0.07 7.2 25.0 Calorimetry Yu Liu 1998
[b-Cyclodextrin](1).[mefenamic acid] 4.74 0.04 Bjerrum method Hladon, Teresa 1999
[b-Cyclodextrin](4).[mefenamic acid] 3.60 0.07 Bjerrum method Hladon, Teresa 1999
[b-Cyclodextrin](1.5).[Lauryl hexaoxyethylene] 5.11 4.00 25.0 Titration microcalorimetry Apryll M. Stalcup 2002
[b-Cyclodextrin](1.5).[Lauryl hexaoxyethylene] 4.30 25.0 capillar zone electrophoresis Apryll M. Stalcup 2002
[b-Cyclodextrin](2).[Triton X-100] 5.26 25.0 titration microcalorimetry Apryll M. Stalcup 2002
[b-Cyclodextrin](1).[Costa-type complex (R=n-C4H9)] 3.55 25.0 1H-NMR Hui-Lan Chen 2003
[b-Cyclodextrin](1).[Costa-type complex (R=n-C6H13)] 4.37 25.0 1H-NMR Hui-Lan Chen 2003
[b-Cyclodextrin](1).[Costa-type complex (R=n-C8H17)] 5.10 25.0 1H-NMR Hui-Lan Chen 2003
[b-Cyclodextrin](1).[Ebselen] 2.68 7.0 25.0 phase solubility Kaneto Uekama 2002
[b-Cyclodextrin](1).[Cyproterone acetate] 3.43 25.0 phase solubility Sandrine Henry De Hassonville 2002
[b-Cyclodextrin](1).[N-(1-adamantylmethyl)-] 4.45 3.48 7.0 25.0 surface plasmon resonance (SPR) Susan E. Brown 2003
[b-Cyclodextrin](1).[N-octyl-] 2.89 1.48 7.0 25.0 surface plasmon resonance (SPR) Susan E. Brown 2003
[b-Cyclodextrin](1).[N-(4-tert-butyl benzyl)-] 3.97 2.78 7.0 25.0 surface plasmon resonance (SPR) Susan E. Brown 2003
[b-Cyclodextrin](1).[p-nitrophenol] 3.34 25.0 Potentiometric titration Kenneth A. Connors 1976
[b-Cyclodextrin](1).[p-nitrophenol] 3.35 25.0 Spectrophotometric method Kenneth A. Connors 1976
[b-Cyclodextrin](1).[p-nitrophenol] 2.41 3.0 30.0 NMR spectroscopy Soledad Penades 1993
[b-Cyclodextrin](1).[p-nitrophenol] 2.82 10.0 30.0 NMR spectroscopy Soledad Penades 1993
[b-Cyclodextrin](1).[p-nitrophenol] 2.70 7.4 23.0 UV-vis spectroscopy Jiri Horsky 1994
[b-Cyclodextrin](1).[p-nitrophenol] 2.27 7.0 30.0 NMR spectroscopy Yoshio Inoue 1992
[b-Cyclodextrin](1).[p-nitrophenol] 2.84 1.18 8.0 25.0 UV-vis spectroscopy Iwao Suzuki 2006
[b-Cyclodextrin](1).[p-nitrophenol] 2.42 5.0 25.0 Differential pulse polarography Carlos Bravo-Diaz 2002
[b-Cyclodextrin](1).[p-nitrophenol] 2.58 14.0 25.0 UV-vis spectroscopy Carlos Bravo-Diaz 2002
[b-Cyclodextrin](1).[p-nitrophenol] 2.89 10.0 25.0 Differential pulse polarography Carlos Bravo-Diaz 2002
[b-Cyclodextrin](1).[p-nitrophenol] 2.11 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[p-nitrophenol] 3.01 10.0 20.0 polarography Kazumi Fujimura 1986
[b-Cyclodextrin](1).[Benzoic acid] 1.58 25.0 Potentiometric titration Kenneth A. Connors 1976
[b-Cyclodextrin](1).[Benzoic acid] 2.55 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Gliclazide] 3.04 13C NMR Moyano, Jose R. 1997
[b-Cyclodextrin](2).[Vitamin A palmitate] 2.27 phase solubility Giovanni Filippo Palmieri 1992
[b-Cyclodextrin](1).[Vitamin A palmitate] -2.66 Fluorescence analysis Giovanni Filippo Palmieri 1992
[b-Cyclodextrin](1).[dipyridamole] -3.26 1H-NMR Torri, G. 1990
[b-Cyclodextrin](1).[dipyridamole] 3.90 5.5 23.0 phase solubility Torri, G. 1990
[b-Cyclodextrin](1).[cyclopenthiazide] 2.22 phase solubility Ahmed M. El-Sayed 1990
[b-Cyclodextrin](1).[cyclopenthiazide] 2.25 UV spectrophotometry Ahmed M. El-Sayed 1990
[b-Cyclodextrin](1).[bendrofluazide] 1.75 phase solubility Ahmed M. El-Sayed 1990
[b-Cyclodextrin](1).[bendrofluazide] 1.78 UV spectrophotometry Ahmed M. El-Sayed 1990
[b-Cyclodextrin](1).[hydroflumethiazide] 1.45 phase solubility Ahmed M. El-Sayed 1990
[b-Cyclodextrin](1).[hydroflumethiazide] 1.47 UV spectrophotometry Ahmed M. El-Sayed 1990
[b-Cyclodextrin](1).[methyl phenyl sulfide] 3.62 Spectrophotometric method Hidetake Sakuraba 1991
[b-Cyclodextrin](1).[isobutyl phenyl sulfide] 3.34 Spectrophotometric method Hidetake Sakuraba 1991
[b-Cyclodextrin](1).[methyl 1-naphthyl sulfide] 3.08 Spectrophotometric method Hidetake Sakuraba 1991
[b-Cyclodextrin](1).[methyl 2-naphthyl sulfide] 3.20 Spectrophotometric method Hidetake Sakuraba 1991
[b-Cyclodextrin](1).[Di-tert-butyl nitroxide ] 2.97 25.0 ESR Yoshimi Sueishi 1991
[b-Cyclodextrin](1).[ibuprofen] 4.01 6.55 25.0 capillary electrophoresis Jetse C. Reijenga 1997
[b-Cyclodextrin](1).[ibuprofen] 3.78 6.55 32.0 capillary electrophoresis Jetse C. Reijenga 1997
[b-Cyclodextrin](1).[ibuprofen] 3.57 6.55 40.0 capillary electrophoresis Jetse C. Reijenga 1997
[b-Cyclodextrin](1).[ibuprofen] 3.48 6.55 50.0 capillary electrophoresis Jetse C. Reijenga 1997
[b-Cyclodextrin](1).[ibuprofen] 4.26 10.0 spectrofluorometry Graciela M. Escandar 2003
[b-Cyclodextrin](1).[ibuprofen] 4.14 25.0 spectrofluorometry Graciela M. Escandar 2003
[b-Cyclodextrin](2).[ibuprofen] 3.72 6.55 25.0 capillary electrophoresis Jetse C. Reijenga 1997
[b-Cyclodextrin](2).[ibuprofen] 3.55 6.55 32.0 capillary electrophoresis Jetse C. Reijenga 1997
[b-Cyclodextrin](2).[ibuprofen] 3.33 6.55 40.0 capillary electrophoresis Jetse C. Reijenga 1997
[b-Cyclodextrin](2).[ibuprofen] 3.22 6.55 50.0 capillary electrophoresis Jetse C. Reijenga 1997
[b-Cyclodextrin](1).[2,3-naphthalimide] 2.89 7.0 25.0 UV and fluorescence spectroscopy Mario J. Politi 1997
[b-Cyclodextrin](1).[2,3-N-butylnaphthalimide] 3.30 7.0 25.0 UV and fluorescence spectroscopy Mario J. Politi 1997
[b-Cyclodextrin](1).[1,8-naphthalimide] 2.15 7.0 25.0 UV and fluorescence spectroscopy Mario J. Politi 1997
[b-Cyclodextrin](1).[1,8-N-butylnaphthalimide] 2.74 7.0 25.0 UV and fluorescence spectroscopy Mario J. Politi 1997
[b-Cyclodextrin](1).[spironolactone] 4.39 phase solubility Kaneto Uekama 1997
[b-Cyclodextrin](1).[spironolactone] 4.00 2.0 25.0 HPLC-method Valentino J. Stella 2000
[b-Cyclodextrin](1).[2-methylbenzoate] 1.11 0.30 7.0 25.0 capillary electrophoresis and HPLC David M. Goodall 1997
[b-Cyclodextrin](1).[3-methylbenzoate] 1.66 0.08 7.0 25.0 capillary electrophoresis and HPLC David M. Goodall 1997
[b-Cyclodextrin](1).[4-methylbenzoate] 1.93 0.40 7.0 25.0 capillary electrophoresis and HPLC David M. Goodall 1997
[b-Cyclodextrin](1).[papaverine] 1.97 7.4 37.0 Higuchi and Connors method G. Puglisi 1998
[b-Cyclodextrin](1).[phenolphthalein] 4.16 2.00 7.0 FIG method Chieu D. Tran 1998
[b-Cyclodextrin](1).[phenolphthalein] 4.35 10.5 FIG method Chieu D. Tran 1998
[b-Cyclodextrin](1).[phenolphthalein] 4.49 10.4 VIS spectroscopy Tsuneo Okubo 1989
[b-Cyclodextrin](1).[phenolphthalein] 4.08 3.20 10.5 25.0 UV/VIS spectroscopy Bruno Szpoganicz 2001
[b-Cyclodextrin](1).[tolmetin] 3.35 1.95 7.0 15.0 conductivity method E. Aicart 1999
[b-Cyclodextrin](1).[tolmetin] 3.33 1.93 7.0 20.0 conductivity method E. Aicart 1999
[b-Cyclodextrin](1).[tolmetin] 3.29 1.90 7.0 25.0 conductivity method E. Aicart 1999
[b-Cyclodextrin](1).[tolmetin] 3.26 1.88 7.0 30.0 conductivity method E. Aicart 1999
[b-Cyclodextrin](1).[tolmetin] 3.23 1.85 7.0 40.0 conductivity method E. Aicart 1999
[b-Cyclodextrin](1).[tolmetin] 3.15 2.00 7.4 absorption spectroscopy, induced circular dichroism Sandra Monti 1999
[b-Cyclodextrin](1).[2-(4'-N,N-dimethylaminophenyl)benzimidazole] 2.69 1.00 8.0 Fluorescence analysis Shen K. Dogra 1999
[b-Cyclodextrin](1).[naphthalene] 2.58 1.54 20.0 steady-state fluorescence measurement Christopher H. Evans 2000
[b-Cyclodextrin](1).[1-octanene] 1.95 HPLC E. Karakhanov 2000
[b-Cyclodextrin](1).[I3-] 2.65 N.A Hiromi Kitano 2000
[b-Cyclodextrin](1).[sodium dodecyl sulfate] 2.32 N.A Ching-Erh Lin 2001
[b-Cyclodextrin](1).[sodium dodecyl sulfate] 4.27 SDS membrane selective electrode Ching-Erh Lin 2001
[b-Cyclodextrin](1).[sodium dodecyl sulfate] 4.32 UV and visible absorbance probe Ching-Erh Lin 2001
[b-Cyclodextrin](1).[sodium dodecyl sulfate] 4.41 Fluorescence analysis Ching-Erh Lin 2001
[b-Cyclodextrin](1).[sodium dodecyl sulfate] 3.64 2.83 7.0 25.0 NMR spectroscopy Qing-Xiang Guo 1994
[b-Cyclodextrin](1).[sodium dodecyl sulfate] 4.26 23.0 Surface plasmon resonance Véronique Wintgens 2005
[b-Cyclodextrin](1).[sodium dodecyl sulfate] 2.48 25.0 conductometric methods Hanqing Wang 1997
[b-Cyclodextrin](1).[sodium dodecyl sulfate] 2.55 conductometric methods Hanqing Wang 1997
[b-Cyclodextrin](1).[sodium dodecyl sulfate] 2.32 conductometry E. Wyn-Jones 1995
[b-Cyclodextrin](1).[sodium dodecyl sulfate] 3.92 surface tension method E. Wyn-Jones 1995
[b-Cyclodextrin](1).[sodium dodecyl sulfate] 4.27 UV/Vis E. Wyn-Jones 1995
[b-Cyclodextrin](1).[sodium dodecyl sulfate] 4.32 Electromotive force E. Wyn-Jones 1995
[b-Cyclodextrin](1).[2-methylnaphthoate] 3.29 2.20 steady-state fluorescence measurement Francisco Mendicuti 1999
[b-Cyclodextrin](1).[2-methylnaphthoate] 3.29 2.20 25.0 steady-state fluorescence spectroscopy Wayne L. Mattice 1998
[b-Cyclodextrin](1).[9-methyl anthracenoate] 2.70 2.28 5.0 steady-state fluorescence measurement Francisco Mendicuti 1999
[b-Cyclodextrin](1).[9-methyl anthracenoate] 2.53 1.48 15.0 steady-state fluorescence measurement Francisco Mendicuti 1999
[b-Cyclodextrin](1).[9-methyl anthracenoate] 2.27 2.00 25.0 steady-state fluorescence measurement Francisco Mendicuti 1999
[b-Cyclodextrin](1).[9-methyl anthracenoate] 2.40 0.95 35.0 steady-state fluorescence measurement Francisco Mendicuti 1999
[b-Cyclodextrin](1).[9-methyl anthracenoate] 2.23 0.95 45.0 steady-state fluorescence measurement Francisco Mendicuti 1999
[b-Cyclodextrin](1).[1-methyl pyrenoate] 1.76 1.49 5.0 steady-state fluorescence measurement Francisco Mendicuti 1999
[b-Cyclodextrin](1).[1-methyl pyrenoate] 1.54 1.65 15.0 steady-state fluorescence measurement Francisco Mendicuti 1999
[b-Cyclodextrin](1).[1-methyl pyrenoate] 1.53 1.68 25.0 steady-state fluorescence measurement Francisco Mendicuti 1999
[b-Cyclodextrin](1).[1-methyl pyrenoate] 1.36 1.73 35.0 steady-state fluorescence measurement Francisco Mendicuti 1999
[b-Cyclodextrin](1).[1-methyl pyrenoate] 1.28 1.75 45.0 steady-state fluorescence measurement Francisco Mendicuti 1999
[b-Cyclodextrin](1).[Sodium fusidate] 2.87 2.11 1H and 13C NMR Wajih Al-Soufi 2003
[b-Cyclodextrin](2).[Sodium fusidate] 2.32 1.88 1H and 13C NMR Wajih Al-Soufi 2003
[b-Cyclodextrin](1).[Potassium helvolate] 3.38 2.94 1H and 13C NMR Wajih Al-Soufi 2003
[b-Cyclodextrin](2).[Potassium helvolate] 1.78 1.95 1H and 13C NMR Wajih Al-Soufi 2003
[b-Cyclodextrin](1).[Procaine hydrochloride] 2.10 5.0 25.0 capillary electrophoresis Guonan Chen 2003
[b-Cyclodextrin](1).[Procaine hydrochloride] 2.14 Constant coulometric titration method Guonan Chen 2003
[b-Cyclodextrin](1).[Procaine hydrochloride] 2.06 Resonance Rayleigh scattering method Guonan Chen 2003
[b-Cyclodextrin](1).[Procaine hydrochloride] 2.03 UV-VIS spectrophotometric method Guonan Chen 2003
[b-Cyclodextrin](1).[Procaine hydrochloride] 2.09 Fluorescence method Guonan Chen 2003
[b-Cyclodextrin](1).[Noradrenaline] 2.73 NMR Seunho Jung 2004
[b-Cyclodextrin](1).[Cholesterol] 3.28 25.0 Potential of mean force Wensheng Cai 2006
[b-Cyclodextrin](1).[propranolol] 2.38 1.61 7.0 25.0 Calorimetry Giuseppina Castronuovo 2006
[b-Cyclodextrin](1).[propranolol] 2.05 0.90 3.0 25.0 Calorimetry Giuseppina Castronuovo 2006
[b-Cyclodextrin](1).[propranolol] 1.81 0.90 1.3 25.0 Calorimetry Giuseppina Castronuovo 2006
[b-Cyclodextrin](1).[1-naphthylacetic acid] 2.85 1.86 11.3 25.0 Calorimetry Giuseppina Castronuovo 2006
[b-Cyclodextrin](1).[Novocaine] 2.42 1.74 1.78 Spectra titration Emilia Iglesias 2005
[b-Cyclodextrin](1).[Novocaine] 2.40 1.70 1.6 Spectra titration Emilia Iglesias 2005
[b-Cyclodextrin](1).[Novocaine] 2.42 0.95 1.3 Spectra titration Emilia Iglesias 2005
[b-Cyclodextrin](1).[Novocaine] 2.44 1.48 1.22 Fluorescence emission measurement Emilia Iglesias 2005
[b-Cyclodextrin](1).[Novocaine] 2.45 1.08 4.33 Fluorescence emission measurement Emilia Iglesias 2005
[b-Cyclodextrin](1).[Novocaine] 3.19 1.83 10.41 Fluorescence emission measurement Emilia Iglesias 2005
[b-Cyclodextrin](1).[Novocaine] 2.33 0.85 4.33 25.0 Kinetic study Emilia Iglesias 2005
[b-Cyclodextrin](1).[Novocaine] 2.36 0.74 4.5 25.0 Kinetic study Emilia Iglesias 2005
[b-Cyclodextrin](1).[Novocaine] 2.34 0.78 4.9 25.0 Kinetic study Emilia Iglesias 2005
[b-Cyclodextrin](1).[Novocaine] 2.47 0.95 13.0 conductivity measurement Emilia Iglesias 2005
[b-Cyclodextrin](1).[Novocaine] 2.47 1.04 17.0 conductivity measurement Emilia Iglesias 2005
[b-Cyclodextrin](1).[Novocaine] 2.47 1.15 21.0 conductivity measurement Emilia Iglesias 2005
[b-Cyclodextrin](1).[Novocaine] 2.45 0.90 25.0 conductivity measurement Emilia Iglesias 2005
[b-Cyclodextrin](1).[Novocaine] 2.89 1.38 13.11 Kinetic study Emilia Iglesias 2005
[b-Cyclodextrin](1).[Novocaine] 2.85 1.15 13.3 Kinetic study Emilia Iglesias 2005
[b-Cyclodextrin](1).[Novocaine] 2.83 1.46 13.4 Kinetic study Emilia Iglesias 2005
[b-Cyclodextrin](1).[Novocaine] 2.82 0.95 13.48 Kinetic study Emilia Iglesias 2005
[b-Cyclodextrin](1).[Acenaphthalene] 2.41 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Acenaphthene] 2.11 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Acenocoumarol anion] 2.68 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Acetaminophen] 2.03 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Acetohexamide] 2.95 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Acetohexamide anion] 3.04 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Acetone] 0.70 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Acetonitrile] 0.78 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[N-Acetylimidazole] 0.85 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Acetylnaphthalene] 2.74 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Acridine] 2.46 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Adamantaneacetic acid anion] 4.30 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Adamantanecarboxylic acid] 5.52 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Adamantanecarboxylic acid anion] 4.30 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Adamantane-2-one-1-carboxylic acid anion] 2.92 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Adenosine 5'-monophosphate anion] 1.61 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Adiphenine] 3.44 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Allobarbital anion] 1.34 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Aminoadamantane] 5.04 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[adamantan-1-yl-ammonium] 4.04 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Aminoadamantane] 3.64 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Aminobenzoic acid] 1.80 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Aminobenzoic acid] 2.70 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Aminocinnamic acid] 2.26 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Aminomethyladamantane cation] 3.48 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Aminonaphthalene-1-sulfonate anion] 1.70 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Aminophthalimide] 2.32 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Aminosalicylic acid] 2.59 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Amitryptylin] 4.38 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Amobarbital] 3.08 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Amobarbital anion] 2.61 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Aniline] 2.10 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Anilinonaphthalene-8-sulfonate anion] 2.04 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Anilinonaphthalene-6-sulfonate anion] 3.32 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Anilinonaphthalene-7-sulfonate anion] 3.11 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Anilinonaphthalene-8-sulfonate anion] 2.11 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Anthracene] 3.36 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Anthranilic acid] 2.11 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[D-Arabinose] 1.21 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[L-Arabinose] -0.15 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Aspartame] 2.11 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Aspartame] 2.18 0.51 7.4 23.0 UV-vis spectroscopy Jiri Horsky 1994
[b-Cyclodextrin](1).[Aspirin] 3.23 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Azapropazone] 1.56 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Barbital] 2.18 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Barbital anion] 2.00 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Beclomethasone dipropionate] 3.05 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Bencyclane] 4.90 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Benoxaprofen] 3.01 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Benoxaprofen anion] 2.85 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Benzaldehyde] 3.25 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Benz[a]anthracene] 3.54 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Benzene] 2.29 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Benzidine] 3.36 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Benzoic acid anion] 1.00 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Benzophenone] 3.18 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Benzo[a]pyrene] 3.34 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-BenzoylBenzoic acid] 2.83 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-BenzoylBenzoic acid anion] 2.18 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-BenzoylBenzoic acid] 3.29 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-BenzoylBenzoic acid anion] 2.76 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-BenzoylBenzoic acid] 3.26 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-BenzoylBenzoic acid anion] 2.80 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Benzoyltrifluoroacetone] 2.62 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Benzyl alcohol] 1.32 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Benzyl alcohol] 1.80 5.8 25.0 UV-Vis spectroscopy Sophie Fourmentin 2006
[b-Cyclodextrin](1).[Betamethasone] 3.73 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Betamethasone] 2.90 2.00 35.0 HPLC Nina Sadlej-Sosnowska 1997
[b-Cyclodextrin](1).[Betamethasone 17-valerate] 3.48 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Bicyclo[2,2,1]heptanecarboxylic acid] 4.18 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Bicyclo[2,2,1]heptanecarboxylic acid anion] 2.92 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Bicyclo[2,2,2]octanecarboxylic acid] 4.99 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Bicyclo[2,2,2]octanecarboxylic acid anion] 3.85 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Biphenylacetic acid] 3.29 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[l-Borneol] 3.08 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Bromazepam] 1.74 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Bromazepam] 1.74 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[b-Cyclodextrin](1).[Bromide anion] 0.23 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Bromobenzene] 2.49 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-BromoBenzoic acid] 3.35 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Bromocinnamic acid] 2.84 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Bromocinnamic acid anion] 2.73 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Bromocinnamic acid] 3.10 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Bromocinnamic acid anion] 3.05 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Bromodiphenhydramine] 3.33 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Bromofluorobenzene] 2.26 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[10-(4-Bromo-1-naphthoyl)-n-decyltrimethylammonium] 2.77 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[(4-Bromo-1-naphthoyl)methyltrimethylammonium] 2.85 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5-(4-Bromo-1-naphthoyl)-n-pentyltrimethylammonium] 2.72 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Bromophenol] 2.93 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Bropirimine] 2.41 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Butabarbital] 2.95 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Butabarbital anion] 2.19 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1,3-Butanediol] 4.08 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Butanol] 1.44 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Butanol] 1.15 25.0 GC Isao Sanemasa 1999
[b-Cyclodextrin](1).[2-Butanol] 1.19 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Butethal] 2.94 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[n-Butylamine] 0.48 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[n-Butyl 4-hydroxybenzoate] 3.33 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-t-Butyl-4-hydroxyphenylazobenzene-4-sulfonate anion] 3.53 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-t-Butyl-4-hydroxyphenylazobenzene-4-sulfonate] 3.23 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-n-Butylphenol] 3.61 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-t-Butylphenyl acetate] 3.89 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Butyric acid] 1.51 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Carbon tetrachloride] 2.18 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Carbon tetrachloride] 2.21 7.0 30.0 Solubility method, titration method Sophie Fourmentin 2006
[b-Cyclodextrin](1).[4-Carboxy-2-nitrophenyl acetate anion] 2.23 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Carboxy-2-nitrophenyl butanoate anion] 2.82 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Carboxy-2-nitrophenyl heptanoate anion] 3.57 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Carboxy-2-nitrophenyl hexanoate anion] 3.42 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Carboxy-2-nitrophenyl octanoate anion] 3.10 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cetyltrimethylammonium] 3.35 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Chenodeoxycholate anion] 4.36 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Chloramine-T anion] 3.18 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Chlorcyclizine] 3.39 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Chlordiazepoxide] 1.36 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Chlordiazepoxide] 1.36 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[b-Cyclodextrin](1).[Chloride anion] 0.11 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Chlorobenzene] 2.20 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-ChloroBenzoic acid] 3.35 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Chlorocinnamic acid] 2.88 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Chlorocinnamic acid anion] 2.70 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Chlorocinnamic acid] 3.05 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Chlorocinnamic acid anion] 2.84 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Chlorocinnamic acid] 2.77 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Chlorocinnamic acid anion] 2.84 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Chlorofluorobenzene] 2.08 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Chloroform] 1.38 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Chloronitrobenzene] 2.36 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Chloronitrobenzene] 2.03 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Chloronitrobenzene] 2.15 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Chlorophenol] 2.61 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Chlorophenyl acetate] 2.46 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Chlorpromazine] 4.04 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Chlorpromazine sulfoxide] 2.70 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cholate anion] 3.04 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[trans-Cinnamic acid] 2.57 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[trans-Cinnamic acid anion] 2.50 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cinnarizine] 3.79 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Clobazam] 1.76 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Clonazepam] 1.90 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Congo Red] 3.22 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cortisone] 3.42 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cortisone acetate] 3.62 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[o-Cresolphthalein] 2.34 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Crystal Violet] 3.42 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Crystal Violet] 3.27 7.2 25.0 UV-vis spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[Cyclizine] 3.08 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cyclobarbital] 3.15 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cyclobarbital anion] 2.15 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cyclobutanol] 1.18 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cyclodecane] 3.21 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cycloheptane] 2.87 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cycloheptanol] 3.23 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cyclohexane] 2.19 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cyclohexaneacetic acid] 3.93 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cyclohexanecarboxylic acid] 3.62 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cyclohexanecarboxylic acid anion] 2.15 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[cis-1,2-Cyclohexanediol] 2.43 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[trans-1,2-cyclohexanediol] 1.79 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cyclohexanol] 2.86 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cyclohexanone] 2.71 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cyclohexylamine] 1.66 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cyclooctane] 3.23 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cyclooctanol] 3.30 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cyclopentane] 1.95 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cyclopentanecarboxylic acid] 3.20 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Cyclopentanol] 2.08 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Dansyl D-alanine anion] 2.25 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Dansyl L-alanine anion] 2.16 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Dansylamide] 1.78 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[n-Decanoic acid] 3.97 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[n-Decanoic acid anion] 3.83 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Decyltrimethylammonium] 2.60 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Dehydrocholate anion] 3.38 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Deoxycholate anion] 3.43 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[D-Deoxyribose] 0.97 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Dexamethasone] 3.67 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Dexamethasone] 2.85 1.60 35.0 HPLC Nina Sadlej-Sosnowska 1997
[b-Cyclodextrin](1).[Dexamethasone acetate] 3.98 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Diacetin] 1.18 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Diazepam] 1.92 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Diazepam] 2.34 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[b-Cyclodextrin](1).[1,4-Dibromobenzene] 2.97 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Di-t-butyl nitroxide] 2.69 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1,4-Dichlorobenzene] 2.51 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Diclofenac acid] 2.18 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Diclofenac acid anion] 2.71 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Dicumarol anion] 3.60 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Dicyclomine] 4.98 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[N,N-Diethylaniline] 2.94 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5,5-Diethylthiobarbituric acid] 2.48 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5,5-Diethylthiobarbituric acid anion] 2.08 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Difenzoquat] 1.91 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Diflunisal anion] 5.26 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1,4-Difluorobenzene] 1.60 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1,2-Dihydroxybenzene] 2.04 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1,3-Dihydroxybenzene] 2.07 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1,4-Dihydroxybenzene] 2.05 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2,4-Dihydroxybenzoic acid] 3.12 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3,4-Dihydroxybenzoic acid] 2.66 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3,4-Dihydroxycinnamic acid] 2.57 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3,4-Dihydroxycinnamic acid anion] 2.56 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1,4-Diiodobenzene] 3.18 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(3,5-Diisopropyl-4-hydroxyphenylazo)benzenesulfonate anion] 3.11 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(3,5-Diisopropyl-4-hydroxyphenylazo)benzenesulfonate] 2.89 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3,4-Dimethoxycinnamic acid] 3.04 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Dimethylaminoazobenzene] 2.69 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Dimethylaminocinnamic acid anion] 3.08 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Dimethylaminocinnamic acid] 2.25 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[N,N-Dimethylaniline] 2.34 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-(2,3-Dimethylanilino)benzoic acid anion] 2.94 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(2,3-Dimethylanilino)benzoic acid anion] 3.17 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3,3-Dimethyl-2-butanol] 2.75 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(3,5-Dimethyl-4,6-dihydroxyphenylazo)benzenesulfonate anion] 3.36 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(3,5-Dimethyl-4,6-dihydroxyphenylazo)benzenesulfonate] 1.52 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[N,N-Dimethylformamide] 0.34 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(2,3-Dimethyl-4-hydroxyphenylazo)benzenesulfonate anion] 3.41 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(2,3-Dimethyl-4-hydroxyphenylazo)benzenesulfonate] 3.32 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(2,5-Dimethyl-4-hydroxyphenylazo)benzenesulfonate anion] 3.08 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(2,5-Dimethyl-4-hydroxyphenylazo)benzenesulfonate] 2.77 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(3,5-Dimethyl-4-hydroxyphenylazo)benzenesulfonate anion] 3.20 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(3,5-Dimethyl-4-hydroxyphenylazo)benzenesulfonate] 2.80 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(2,6-Dimethyl-4-hydroxyphenylazo)benzenesulfonate anion] 3.04 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(2,6-Dimethyl-4-hydroxyphenylazo)benzenesulfonate] 2.80 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1,4-Dimethylnaphthalene] 2.54 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1,5-Dimethylnaphthalene] 2.30 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1,8-Dimethylnaphthalene] 1.23 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3,5-Dimethylphenyl acetate] 2.06 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2,2-Dimethyl-1-propanol] 2.76 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Dimethylsulfoxide] 0.11 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3,5-DinitroBenzoic acid] 3.62 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3,5-DinitroBenzoic acid anion] 3.10 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Dinitrophenyl-D-leucine anion] 2.94 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Dinitrophenyl-L-leucine anion] 3.15 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Dinitrophenyl-D-methionine anion] 2.75 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Dinitrophenyl-L-methionine anion] 2.86 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Dinitrophenyl-D-valine anion] 2.63 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Dinitrophenyl-L-valine anion] 2.75 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Diphenhydramine] 3.11 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Diphenidol] 2.97 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Diphenylamine] 2.90 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Diphenylhydantoin] 2.93 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Diphenylhydantoin anion] 2.16 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Diphenylpyraline] 3.36 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Dodecylammonium] 3.68 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Dodecylbenzenesulfonate anion] 3.85 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Dodecylpyridinium] 3.70 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Dodecylsulfate anion] 4.41 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Dodecyltrimethylammonium] 3.69 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Doxepin] 4.12 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Ephedrine] 2.25 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Ethanol] 0.08 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Ethoxybenzene] 2.46 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Ethyl 4-aminobenzoate] 2.63 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Ethylbenzene] 2.52 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-(4-Ethylbenzoyl)benzoic acid anion] 3.12 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(4-Ethylbenzoyl)benzoic acid anion] 3.05 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5-Ethyl-5-n-butylbarbituric acid] 2.68 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5-Ethyl-5-n-butylbarbituric acid anion] 2.11 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5-Ethyl-5-n-butylthiobarbituric acid] 2.88 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5-Ethyl-5-n-butylthiobarbituric acid anion] 2.18 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Ethylene glycol] -0.15 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5-Ethyl-5-n-heptylbarbituric acid] 3.72 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5-Ethyl-5-n-heptylbarbituric acid anion] 3.24 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5-Ethyl-5-n-hexylbarbituric acid] 3.46 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5-Ethyl-5-n-hexylbarbituric acid anion] 2.91 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5-Ethyl-5-n-hexylthiobarbituric acid] 3.68 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5-Ethyl-5-n-hexylthiobarbituric acid anion] 3.05 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Ethyl 4-hydroxybenzoate] 3.14 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(3-Ethyl-4-hydroxyphenylazo)benzenesulfonate anion] 3.68 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(3-Ethyl-4-hydroxyphenylazo)benzenesulfonate] 3.26 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Ethyl-3-pentanol] 2.28 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5-Ethyl-5-n-pentylbarbituric acid] 3.11 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5-Ethyl-5-n-pentylbarbituric acid anion] 2.54 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5-Ethyl-5-n-pentylthiobarbituric acid] 3.32 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5-Ethyl-5-n-pentylthiobarbituric acid anion] 2.72 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Ethylphenol] 2.69 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Ethylphenyl acetate] 2.66 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5-Ethyl-5-n-propylbarbituric acid] 2.26 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5-Ethyl-5-n-propylbarbituric acid anion] 2.04 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5-Ethyl-5-n-propylthiobarbituric acid] 2.48 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5-Ethyl-5-n-propylthiobarbituric acid anion] 2.11 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Femoxetine] 3.70 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Ferrocenemonocarboxylic acid anion] 3.38 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Fludiazepam] 2.34 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Fludiazepam] 2.34 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[b-Cyclodextrin](1).[Flufenamic acid] 3.14 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Flufenamic acid anion] 3.13 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Flunitrazepam] 2.11 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Fluocinolone acetonide] 3.48 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Fluoranthene] 2.20 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Fluorene] 3.17 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Fluoroanisole] 1.04 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Fluorobenzene] 1.85 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Flurazepam] 2.08 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Flurbiprofen] 3.71 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Flurbiprofen] 3.23 4.5 25.0 UV-vis spectroscopy P. Mura 2005
[b-Cyclodextrin](1).[Flurbiprofen] 3.16 4.5 37.0 UV-vis spectroscopy P. Mura 2005
[b-Cyclodextrin](1).[Flurbiprofen] 2.77 5.5 25.0 UV-vis spectroscopy P. Mura 2005
[b-Cyclodextrin](1).[Flurbiprofen] 2.73 5.5 37.0 UV-vis spectroscopy P. Mura 2005
[b-Cyclodextrin](1).[Flurbiprofen] 3.78 5.5 25.0 Capillary electrophoresis P. Mura 2005
[b-Cyclodextrin](1).[Flurbiprofen] 3.62 5.5 37.0 Capillary electrophoresis P. Mura 2005
[b-Cyclodextrin](1).[Flurbiprofen anion] 3.29 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Furosemide] 1.79 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Furosemide anion] 2.27 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Glycerol] -0.30 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Glycochenodeoxycholate anion] 4.50 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Glycocholate anion] 3.29 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[n-Heptane] 1.84 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Heptanol] 2.85 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Heptanol] 2.99 0.95 25.0 GC Isao Sanemasa 1999
[b-Cyclodextrin](1).[n-Hexane] 1.78 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[n-Hexanoic acid] 2.47 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[n-Hexanoic acid anion] 1.83 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Hexanol] 2.45 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Hexanol] 2.41 1.00 25.0 GC Isao Sanemasa 1999
[b-Cyclodextrin](1).[2-Hexanol] 1.98 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Hexobarbital] 3.11 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Hexobarbital anion] 2.58 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Homoadamantanecarboxylic acid anion] 4.64 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Hydrocinnamic acid] 2.30 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Hydrocortisone] 3.43 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Hydrocortisone acetate] 3.51 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Hydrocortisone butyrate] 3.38 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Hydroxyadamantane] 4.48 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Hydroxybenzoic acid] 2.46 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Hydroxybenzoic acid] 2.72 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Hydroxybenzoic acid anion] 2.39 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Hydroxycinnamic acid] 2.58 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Hydroxycinnamic acid] 2.63 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Hydroxycinnamic acid anion] 2.37 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Hydroxycinnamic acid] 2.76 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Hydroxycinnamic acid anion] 2.61 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Hydroxycoumarin anion] 2.20 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Hydroxyethylphenol] 2.52 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-[(2-Hydroxy-3-isobutylamino)propoxy]phenylcarbamic acid, n-pentyl ester] 2.64 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-[(2-Hydroxy-3-isopropylamino)propoxy]phenylcarbamic acid, methyl ester] 2.33 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-[(2-Hydroxy-3-isopropylamino)propoxy]phenylcarbamic acid, n-pentyl ester] 2.66 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-[(2-Hydroxy-3-isopropylamino)propoxy]phenylcarbamic acid, n-propyl ester] 2.51 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Hydroxymethylphenol] 2.16 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(4-Hydroxy-1-naphthylazo)benzenesulfonate anion] 2.61 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(4-Hydroxy-1-naphthylazo)naphthalene-1-sulfonate anion] 3.40 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(4-Hydroxyphenylazo)benzenesulfonate anion] 3.30 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(4-Hydroxyphenylazo)benzenesulfonate] 3.20 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(p-Hydroxyphenyl)-3-isonicotinoyl-2-pyrazoline] 3.42 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(p-Hydroxyphenyl)-3-nicotinoyl-2-pyrazoline] 3.10 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(p-Hydroxyphenyl)-3-picolinoyl-2-pyrazoline] 3.28 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Hydroxypropylphenol] 2.98 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Hydroxypyridine] 2.36 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Imidazole] 0.28 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Imipramine] 3.94 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Indole] 2.26 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Indole] 2.23 1.08 7.0 18.0 HPLC-method Arantza Zornoza 2005
[b-Cyclodextrin](1).[Indomethacin] 2.72 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Indomethacin anion] 2.72 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Iodate anion] 0.00 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Iodide anion] 0.64 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Iodobenzene] 2.90 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Iodofluorobenzene] 2.71 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Isopropylbenzene] 3.08 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(3-Isopropyl-4-hydroxyphenylazo)benzenesulfonate anion] 3.40 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(3-Isopropyl-4-hydroxyphenylazo)benzenesulfonate] 3.23 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Ketoprofen anion] 3.43 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Lauryl sulfate anion] 2.55 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Lorazepam] 2.51 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[D-Lyxose] 0.63 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[D-Mandelic acid anion] 1.26 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[L-Mandelic acid anion] 1.23 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Maprotilin] 3.68 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Meclizine] 3.35 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Meclofenamic acid] 2.67 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Meclofenamic acid anion] 2.81 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Medazepam] 2.41 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Medazepam] 2.41 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[b-Cyclodextrin](1).[Mefenamic acid] 2.76 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Mefenamic acid anion] 2.80 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Menadione] 2.28 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Meperidine] 2.13 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Mephobarbital] 3.18 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Mephobarbital anion] 2.11 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Methanol] -0.40 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Metharbital] 2.28 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Metharbital anion] 2.18 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-(4-Methoxyanilino)naphthalene-6-sulfonate anion] 2.98 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Methoxybenzene] 2.14 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Methoxycinnamic acid] 1.79 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Methoxycinnamic acid] 2.65 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Methoxycinnamic acid anion] 2.59 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Methoxycinnamic acid] 2.82 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Methoxycinnamic acid anion] 2.53 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Methylacetanilide] 1.11 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Methylacetanilide] 1.64 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Methylacetanilide] 2.00 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[N-Methylaniline] 1.72 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-N-Methylanilinonaphthalene-6-sulfonate anion] 3.87 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Methylbenzoic acid] 7.11 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Methylbenzoic acid] 3.23 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Methylbenzoic acid anion] 2.04 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Methylbenzophenone] 3.66 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Methylbenzophenone] 3.14 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Methylbenzophenone] 2.89 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-(4-Methylbenzoyl)benzoic acid anion] 2.70 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(4-Methylbenzoyl)benzoic acid anion] 2.96 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Methyl-1-butanol] 2.08 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Methyl-1-butanol] 2.25 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Methyl-2-butanol] 1.91 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Methyl-2-butanol] 1.92 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Methylcinnamic acid] 2.62 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Methylcinnamic acid] 2.98 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Methylcinnamic acid anion] 2.53 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Methylcinnamic acid] 2.64 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Methylcinnamic acid anion] 2.67 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Methylcyclohexanol] 2.08 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Methylcyclohexanone] 2.74 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Methylene Blue] 2.96 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Methyl gallate] 2.10 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Methyl-2-hexanol] 2.33 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(3-Methyl-4-hydroxyphenylazo)benzenesulfonate anion] 3.30 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(3-Methyl-4-hydroxyphenylazo)benzenesulfonate] 3.18 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Methyl-4-(4'-hydroxystyryl)pyridinium] 2.38 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Methylnaphthalene] 2.76 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Methylnaphthalene] 2.85 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Methyl Orange anion] 3.59 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Methyl Orange] 2.60 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Methyl Orange] 3.55 7.2 25.0 Circular dichroism spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[2-Methyl-2-pentanol] 1.99 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Methyl-3-pentanol] 2.15 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Methyl-2-pentanol] 2.04 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Methylphenol] 2.12 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Methylphenol] 2.34 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Methylphenol] 2.61 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[N-Methyl-N-phenyl-2-aminonaphthalene-6-sulfonate anion] 4.40 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Methyl-1-propanol] 1.67 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Methyl-2-propanol] 1.73 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-[3-(2-Methyl-n-propyl)-4-hydroxyphenylazo]benzenesulfonate anion] 3.62 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-[3-(2-Methyl-n-propyl)-4-hydroxyphenylazo]benzenesulfonate] 3.38 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Methyl Red anion] 3.58 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Methyl Red] 3.50 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5-Methylresorcinol] 1.68 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Metronidazole benzoate] 3.08 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Monoacetin] 1.20 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Morphine] 1.49 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Morpholine] 1.23 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Naphthacene] 3.53 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Naphthalene] 2.84 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2,7-Naphthalenedisulfonate] 2.44 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Naphthalenesulfonate anion] 3.40 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Naphthalenesulfonate anion] 5.37 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2,3,6-Naphthalenetrisulfonate] 2.22 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Naphthol] 2.09 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Naphthol anion] 1.63 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Naphthol] 2.75 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Naphthol anion] 1.85 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[a-Naphtholphthalein] 2.78 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Naphthoyltrifluoroacetone] 3.12 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Naphthylamine] 3.36 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Naphthylamine cation] 2.30 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Naphthylamine] 3.81 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Naphthylamine cation] 2.35 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Naphthylacetic acid anion anion] 2.00 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Naphthyloxyacetic acid anion] 2.75 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Naproxen] 3.14 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Naproxen] 3.98 1.95 2.0 15.0 Fluorescence spectroscopy I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen] 3.76 1.95 2.0 25.0 Fluorescence spectroscopy I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen] 3.58 2.46 2.0 35.0 Fluorescence spectroscopy I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen] 3.40 2.41 2.0 45.0 Fluorescence spectroscopy I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen] 3.89 1.90 3.0 15.0 Fluorescence spectroscopy I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen] 3.71 2.80 3.0 25.0 Fluorescence spectroscopy I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen] 3.53 2.41 3.0 35.0 Fluorescence spectroscopy I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen] 3.36 2.08 3.0 45.0 Fluorescence spectroscopy I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen] 3.74 2.43 4.0 15.0 Fluorescence spectroscopy I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen] 3.57 2.76 4.0 25.0 Fluorescence spectroscopy I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen] 3.39 1.70 4.0 35.0 Fluorescence spectroscopy I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen] 3.23 4.0 45.0 Fluorescence spectroscopy I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen] 3.48 1.48 5.0 15.0 Fluorescence spectroscopy I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen] 3.19 1.60 5.0 25.0 Fluorescence spectroscopy I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen] 3.06 2.00 5.0 35.0 Fluorescence spectroscopy I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen] 3.00 1.95 5.0 45.0 Fluorescence spectroscopy I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen] 3.32 1.85 6.0 15.0 Fluorescence spectroscopy I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen] 3.17 1.85 6.0 25.0 Fluorescence spectroscopy I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen] 3.05 6.0 35.0 Fluorescence spectroscopy I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen] 2.87 1.30 6.0 45.0 Fluorescence spectroscopy I. Vélaz 1997
[b-Cyclodextrin](1).[Naproxen anion] 1.43 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Niflumic acid anion] 2.72 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Nimetazepam] 1.74 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Nitrate anion] 0.46 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Nitrazepam] 1.98 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Nitroaniline] 3.12 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Nitroaniline] 3.16 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Nitroaniline] 2.41 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-NitroBenzoic acid] 3.08 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-NitroBenzoic acid anion] 2.77 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-NitroBenzoic acid] 3.08 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-NitroBenzoic acid anion] 3.03 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-NitroBenzoic acid] 2.34 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-NitroBenzoic acid anion] 3.17 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Nitrocinnamic acid] 2.68 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Nitrocinnamic acid] 1.76 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Nitrocinnamic acid] 2.38 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Nitrocinnamic acid anion] 2.52 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Nitrophenol] 2.16 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Nitrophenol anion] 2.00 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Nitrophenol] 2.11 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Nitrophenol anion] 1.88 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Nitrophenol] 2.50 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Nitrophenol anion] 2.80 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Nitrophenyl acetate] 1.72 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Nitrophenyl acetate] 2.19 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Nitrophenylazo-2'-hydroxy-6'-sulfonaphthalene anion] 2.89 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Nitrophenyl butyrate] 2.41 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Nitrophenyl dodecanoate] 3.12 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Nitrophenyl hexanoate] 2.64 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Nitrophenyl 4-nitrobenzoate] 0.64 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Nitrophenyl octanoate] 2.72 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[S-Nitroso-N-acetylpenicillamine] 2.22 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Nocloprost] 3.37 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[n-Nonane] 1.95 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Noradamantanecarboxylic acid] 5.15 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3-Noradamantanecarboxylic acid anion] 3.70 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Norbornaneacetic acid] 4.08 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Norbornaneacetic acid anion] 3.79 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[n-Octane] 1.88 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[n-Octanoic acid] 3.21 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[n-Octanoic acid anion] 2.85 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Octanol] 3.25 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Octanol] 3.28 1.00 25.0 GC Isao Sanemasa 1999
[b-Cyclodextrin](1).[2-Octanol] 3.13 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Orphenadrine] 3.11 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Oxazepam] 2.23 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[n-Pentane] 1.70 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[n-Pentanoic acid] 1.96 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Pentanol] 1.88 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Pentanol] 1.79 -1.00 25.0 GC Isao Sanemasa 1999
[b-Cyclodextrin](1).[2-Pentanol] 1.49 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Pentanol] 1.40 25.0 GC Isao Sanemasa 1999
[b-Cyclodextrin](1).[3-Pentanol] 1.73 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Pentobarbital] 3.02 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Pentobarbital anion] 2.59 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Perchlorate anion] 1.30 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Perfluorobutyric acid anion] 2.31 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Perfluoroheptanoic acid anion] 3.89 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Perfluorononanoic acid anion] 3.86 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Perfluorooctanoic acid anion] 4.34 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Phenacetin] 2.25 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Phenanthrene] 3.18 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Phencyclidine] 3.01 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Phenobarbital] 3.22 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Phenobarbital anion] 2.20 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Phenol] 1.97 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Phenol] 2.34 6.9 40.0 UV-vis spectroscopy Yoshimi Sueishi 2003
[b-Cyclodextrin](1).[Phenol anion] 1.18 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Phenolphthalein] 4.56 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Phenol Red anion] 2.89 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Phenol Red] 2.36 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[N-Phenylanthranilic acid] 2.66 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[N-Phenylanthranilic acid anion] 2.96 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Phenylbutazone] 2.85 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Phenylethanol] 2.15 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Phenylethylamine] 1.91 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Phenyl-3-isonicotinoyl-2-pyrazoline] 3.01 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Phenyl-3-nicotinoyl-2-pyrazoline] 2.97 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[5-Phenyl-2,4-pentadienoic acid] 2.86 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-Phenyl-3-picolinoyl-2-pyrazoline] 2.66 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[S-2-Phenylpropanoic acid] 3.00 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[S-2-Phenylpropanoic acid anion] 1.72 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[R-2-Phenylpropanoic acid] 3.04 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[R-2-Phenylpropanoic acid anion] 1.80 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Phloridzin] 3.01 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Piperidine] 1.71 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Prednisolone] 3.56 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Prednisolone] 2.75 1.70 35.0 HPLC Nina Sadlej-Sosnowska 1997
[b-Cyclodextrin](1).[Prednisolone acetate] 3.76 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Prednisolone acetate] 2.76 1.48 35.0 HPLC Nina Sadlej-Sosnowska 1997
[b-Cyclodextrin](1).[Proadifen] 2.96 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Progesterone] 4.39 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1-Propanol] 0.70 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[2-Propanol] 0.90 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[n-Propylbenzene] 1.66 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1,2-Propylene glycol] 0.28 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[n-Propyl 4-hydroxybenzoate] 2.97 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(3-n-Propyl-4-hydroxyphenylazo)benzenesulfonate anion] 3.75 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-(3-n-Propyl-4-hydroxyphenylazo)benzenesulfonate] 3.46 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[4-n-Propylphenol] 3.42 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Prostaglandin F2a] 2.84 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Prostaglandin F2a anion] 2.51 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Pyrazine] 1.22 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Pyrazine-2-carboxylic acid anion] 1.18 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Pyrene] 2.11 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[D-Ribose] 0.72 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Salicyclic acid] 2.63 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Secobarbital] 3.26 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Secobarbital anion] 2.36 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Sorbic acid] 1.72 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Sulfapyridine] 2.66 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Sulfamethizole anion] 2.74 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Sulfamonomethoxine anion] 2.40 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Sulfanilamide] 2.54 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Sulfaphenazole anion] 2.04 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Sulfisomezole anion] 2.78 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Sulfisoxazole anion] 2.51 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Taurochenodeoxycholate anion] 5.04 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Taurocholate anion] 3.42 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Tauroursodeoxycholate anion] 4.91 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Testosterone] 3.70 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Tetrabromophenolphthalein] 2.60 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Tetradecyltrimethylammonium] 4.07 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Tetrafluoroborate anion] 0.97 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Tetraphenylarsonium] 2.35 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Tetraphenylborate anion] 2.38 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Tetraphenylphosphonium] 2.69 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Thiocyanate anion] 1.00 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Thiopental] 3.43 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Thiopental anion] 2.59 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Thiophenobarbital] 3.60 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Thiophenobarbital anion] 2.95 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Tolnaftate] 3.85 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Toluene] 2.15 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Toluene] 2.15 7.0 30.0 Solubility method, titration method Sophie Fourmentin 2006
[b-Cyclodextrin](1).[2-Toluidinylnaphthalene-6-sulfonate anion] 3.30 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Triacetin] 1.15 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Triamcinolone] 3.37 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Triamcinolone acetonide] 3.51 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Triamcinolone diacetate] 3.55 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Trifluoroacetanilide] 1.94 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1,3,5-Trihydroxybenzene] 2.04 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3,4,5-TrihydroxyBenzoic acid] 2.06 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1,2,3-Trimethylbenzene] 2.26 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1,2,4-Trimethylbenzene] 2.94 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[1,3,5-Trimethylbenzene] 1.78 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[3,4,5-Trimethylphenyl acetate] 2.30 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Triprolidine] 2.42 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Tropaeolin anion] 2.85 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Tropicamide] 2.63 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Ursodeoxycholate anion] 4.51 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[d-Valerolactam] 1.40 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[Warfarin] 3.06 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[o-Xylene] 2.32 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[m-Xylene] 2.20 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[p-Xylene] 2.36 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[D-Xylose] 1.22 25.0 Kenneth A. Connors 1995
[b-Cyclodextrin](1).[{(+)-(3S,4R)-3-ethyl-4-[(1-methyl.5-imidazolyl)-metyl]-tetrahydrofuran-2-on}] 1.98 0.07 7.0 25.0 Potentiometry Lajos Barcza 2006
[b-Cyclodextrin](1).[[(−)-(8S,9R)-6'-methoxy-cinchonanol]] 3.09 0.08 7.0 25.0 Potentiometry Lajos Barcza 2006
[b-Cyclodextrin](1).[chiral N-imidazole derivative 1 (R enantiomer)] 2.37 27.0 NMR spectroscopy Claude Vaccher 2006
[b-Cyclodextrin](1).[chiral N-imidazole derivative 1 (S enantiomer)] 2.22 28.0 NMR spectroscopy Claude Vaccher 2006
[b-Cyclodextrin](1).[n-Octanol] 3.17 2.59 7.0 25.0 Fluorescence spectroscopy Xinzhen Du 2006
[b-Cyclodextrin](1).[Polyethylene glycol (n = 10) n-octylphenyl ether] 3.87 3.26 7.0 25.0 Fluorescence spectroscopy Xinzhen Du 2006
[b-Cyclodextrin](1).[polyethylene glycol (n = 10) tertoctylphenyl ether] 5.26 4.18 7.0 25.0 Fluorescence spectroscopy Xinzhen Du 2006
[b-Cyclodextrin](1).[polyethylene glycol (n = 10) tertoctylphenyl ether in reduced form] 5.59 4.56 7.0 25.0 Fluorescence spectroscopy Xinzhen Du 2006
[b-Cyclodextrin](1).[1-Bromonaphthalene] 2.70 1.88 7.0 25.0 Fluorescence spectroscopy Xinzhen Du 2006
[b-Cyclodextrin](1).[1-Bromonaphthalene] 6.51 5.89 7.0 25.0 Fluorescence and phosporescence spectroscopy Xinzhen Du 2005
[b-Cyclodextrin](1).[phenolphthelein] 4.43 2.90 10.5 25.0 Fluorescence spectroscopy Xinzhen Du 2006
[b-Cyclodextrin](1).[4-tert-butylcatechol] 3.98 3.30 25.0 NMR spectroscopy Dona1 H. Macartney 1993
[b-Cyclodextrin](1).[4-tert-butylcatechol] 3.07 2.18 25.0 UV-vis spectroscopy Dona1 H. Macartney 1993
[b-Cyclodextrin](1).[N-acetyl-L-phenylalanine] 1.78 0.11 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[N-acetyl-L-phenylalanine] 1.83 0.15 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[N-acetyl-L-tryptophan] 1.10 -0.30 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[N-acetyl-L-tyrosine] 2.10 0.30 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[N-acetyl-L-tyrosine] 2.11 0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[N-acetyl-L-tyrosine] 2.11 0.30 6.9 25.0 Isothermal titration calorimetry Yoshihisa Inoue 2004
[b-Cyclodextrin](1).[(1S,2R)-2-amino-1,2-diphenylethanol ] 1.74 0.48 4.8 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(S)-benzylglycidyl ether ] 2.37 1.08 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[2,3-O-benzylidene-L-threitol ] 2.07 0.30 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(2S,3S)-3-benzyloxy-1,2,4-butanetriol ] 1.92 0.30 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[O-benzyl-L-serine] 1.85 0.60 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[N-t-Boc-L-alanine ] 2.59 0.60 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[N-t-Boc-L-alanine methyl ester] 2.82 0.78 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[N-t-Boc-L-alanine methyl ester] 2.76 0.60 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[N-t-Boc-L-serine] 2.49 0.30 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(S)-3-bromo-8-camphorsulfonic acid ] 3.58 2.00 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(S)-3-bromo-2-methyl-1propanol ] 2.15 0.60 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(S)-3-bromo-2-methylpropionic acid methyl ester] 2.42 1.40 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(S)-camphanic acid] 2.25 0.30 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(1S,3R)-camphoric acid] 1.28 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(S)-camphorquinone-3-oxime] 3.42 1.60 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(S)-camphorquinone-3-oxime] 3.39 1.48 4.8 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(S)-10-camphorsulfonic acid] 2.75 1.00 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[N-Cbz-L-alanine ] 2.17 0.60 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[N-Cbz-L-alanine ] 2.17 0.60 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(1S,2S)-trans-1,2-cyclohexanediol ] 1.93 0.30 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(S)-1-cyclohexylethylamine ] 2.52 0.48 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[O,O'-dibenzoyl-L-tartaric acid ] 1.51 0.30 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(S)-N,N-dimethyl-1-ferrocenylethylamine ] 3.75 2.48 4.8 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[O,O'-di-p-toluoyl-L-tartaric acid ] 2.02 0.78 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[Gly-L-Phe ] 1.67 6.1 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[Gly-L-Phe ] 1.88 7.4 23.0 UV-vis spectroscopy Jiri Horsky 1994
[b-Cyclodextrin](1).[(S)-hexahydromandelic acid ] 2.81 1.08 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(1S,2S,5S)-2-hydroxy-3-pinanone ] 3.37 1.95 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(S)-mandelic acid ] 1.04 0.30 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(S)-mandelic acid methyl ester ] 1.83 0.30 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(S)-mandelic acid methyl ester ] 1.78 0.48 4.8 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(S)-a-methoxy phenylacetic acid ] 1.04 0.30 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(S)-a-methoxy-a-trifluoromethyl phenylacetic acid] 2.24 0.30 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[3-Alkoxyl-2-hydroxypropyl trimethyl ammonium bromides] 0.03 7.0 25.0 Calorimetry De-Zhi Sun 2005
[b-Cyclodextrin](1).[L-phenylalanine amide] 2.00 10.0 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[L-phenylalanine methyl ester ] 1.04 0.30 4.8 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(S)-2-phenylbutyric acid] 1.97 0.30 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(S)-3-phenylbutyric acid] 2.60 0.60 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(S)-1-phenyl-1,2-ethanediol ] 1.79 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[azulene] 2.89 2.18 7.0 25.0 Absorption and fluorescence spectroscopy, induced-cirular dicroism spectroscopy Osama K. Abou-Zied 2005
[b-Cyclodextrin](1).[(S)-phenyllactic acid] 1.94 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(S)-2-phenylpropionic acid ] 1.53 0.30 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(1S,2S,3R,5S)-pinanediol ] 3.81 2.08 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(S)-propranolol ] 2.06 1.00 4.8 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[benzyloxyacetaldehyde dimethyl acetal ] 2.34 1.40 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[3-bromo-1-propanol ] 1.34 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](0.5).[3-Alkoxyl-2-hydroxypropyl trimethyl ammonium bromides] 2.15 7.0 25.0 Calorimetry De-Zhi Sun 2005
[b-Cyclodextrin](1).[N-Cbz-glycine] 2.20 0.60 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[N-Cbz-L-serine ] 2.04 0.30 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[cyclohexanol ] 2.85 0.78 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[cyclohexanol ] 2.85 0.78 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[cyclohexanol ] 2.85 0.60 7.2 25.0 Microcalorimetric titrations Yu Liu 2003
[b-Cyclodextrin](1).[cyclohexanol ] 2.85 0.78 Microcalorimetric titrations Yu Liu 2003
[b-Cyclodextrin](1).[cyclohexanol ] 2.85 0.60 7.2 25.0 titration microcalorimetry Yu Liu 2004
[b-Cyclodextrin](1).[cyclohexanol ] 2.58 1.53 7.0 27.0 NMR spectroscopy Carlos Jaime 2005
[b-Cyclodextrin](1).[cyclohexanol ] 2.85 Isothermal microcalorimetric titration Carlos Jaime 2005
[b-Cyclodextrin](1).[cyclohexylacetic acid ] 3.10 1.78 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[1-methyl-3-phenylpropylamine ] 2.27 0.48 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[1-methyl-3-phenylpropylamine ] 2.27 0.48 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[4-phenyl butylamine ] 2.61 0.78 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[(+,-)-3-phenylbutyric acid ] 2.62 0.70 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[3-phenylpropionic acid ] 2.21 0.60 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[3-phenylpropionic acid ] 2.21 0.60 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[3-ethoxy propylamine] 0.90 0.60 6.9 25.0 Microcalorimetry Yoshihisa Inoue 2000
[b-Cyclodextrin](1).[1-butanol] 1.23 7.2 25.0 Differential circular dichroism spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[1-butanol] 1.35 0.30 1.0 25.0 UV-vis spectroscopy L. Garcia-Rio 2005
[b-Cyclodextrin](1).[1-butanol] 1.20 0.30 6.9 25.0 Titration calorimetry Robert N. Goldberg 1994
[b-Cyclodextrin](1).[Methyl orange] 3.40 5.8 25.0 UV-Vis spectroscopy Sophie Fourmentin 2006
[b-Cyclodextrin](1).[1-pentanol ] 1.80 7.2 25.0 Differential circular dichroism spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[1-hexanol] 2.34 7.2 25.0 Differential circular dichroism spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[1-hexanol] 2.17 0.99 1.0 25.0 UV-vis spectroscopy L. Garcia-Rio 2005
[b-Cyclodextrin](1).[cyclopentanol] 2.24 7.2 25.0 Differential circular dichroism spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[cyclopentanol] 2.24 0.70 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[cyclopentanol] 2.23 0.48 7.2 25.0 titration microcalorimetry Yu Liu 2004
[b-Cyclodextrin](1).[cyclopentanol] 3.21 2.11 7.0 27.0 NMR spectroscopy Carlos Jaime 2005
[b-Cyclodextrin](1).[cyclopentanol] 2.23 Isothermal microcalorimetric titration Carlos Jaime 2005
[b-Cyclodextrin](1).[cyclopentanol] 2.08 7.2 25.0 UV-vis spectroscopy Yu Liu 1998
[b-Cyclodextrin](1).[cyclohexanol] 2.85 7.2 25.0 Differential circular dichroism spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[cyclohexanol] 2.70 7.2 25.0 UV-vis spectroscopy Yu Liu 1998
[b-Cyclodextrin](1).[cycloheptanol] 3.34 7.2 25.0 Differential circular dichroism spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[cycloheptanol] 3.34 1.85 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[cycloheptanol] 3.06 1.98 7.0 27.0 NMR spectroscopy Carlos Jaime 2005
[b-Cyclodextrin](1).[cycloheptanol] 3.37 Isothermal microcalorimetric titration Carlos Jaime 2005
[b-Cyclodextrin](1).[cyclooctanol ] 3.64 7.2 25.0 Differential circular dichroism spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[cyclooctanol ] 3.65 7.2 25.0 titration microcalorimetry Yu Liu 2004
[b-Cyclodextrin](1).[Eugenol] 2.51 5.8 25.0 UV-Vis spectroscopy Sophie Fourmentin 2006
[b-Cyclodextrin](1).[Isoeugenol] 2.48 5.8 25.0 UV-Vis spectroscopy Sophie Fourmentin 2006
[b-Cyclodextrin](1).[Anisyl alcohol] 2.03 5.8 25.0 UV-Vis spectroscopy Sophie Fourmentin 2006
[b-Cyclodextrin](1).[ursodeoxycholic acid] 3.55 7.4 24.0 HPLC-method G. Puglisi 1997
[b-Cyclodextrin](1).[ursodeoxycholic acid] 3.12 7.4 37.0 HPLC-method G. Puglisi 1997
[b-Cyclodextrin](1).[ursodeoxycholic acid] 2.66 7.4 45.0 HPLC-method G. Puglisi 1997
[b-Cyclodextrin](1).[ursodeoxycholic acid] 3.89 5.5 25.0 HPLC-method I. Orienti 1999
[b-Cyclodextrin](1).[ursodeoxycholic acid] 3.71 5.5 30.0 HPLC-method I. Orienti 1999
[b-Cyclodextrin](1).[ursodeoxycholic acid] 3.19 5.5 37.0 HPLC-method I. Orienti 1999
[b-Cyclodextrin](1).[ursodeoxycholic acid] 3.63 7.0 25.0 HPLC-method I. Orienti 1999
[b-Cyclodextrin](1).[ursodeoxycholic acid] 3.50 7.0 30.0 HPLC-method I. Orienti 1999
[b-Cyclodextrin](1).[ursodeoxycholic acid] 3.21 7.0 37.0 HPLC-method I. Orienti 1999
[b-Cyclodextrin](1).[chenodeoxycholic acid] 2.77 7.4 25.0 HPLC-method G. Puglisi 1997
[b-Cyclodextrin](1).[aromatic norbornadiene derivative 2] 2.49 1.65 25.0 Fluorescence spectroscopy Jean-Jacques Aaron 1998
[b-Cyclodextrin](1).[aromatic norbornadiene derivative 3] 2.59 1.54 25.0 Fluorescence spectroscopy Jean-Jacques Aaron 1998
[b-Cyclodextrin](1).[aromatic norbornadiene derivative 4] 2.52 1.70 25.0 Fluorescence spectroscopy Jean-Jacques Aaron 1998
[b-Cyclodextrin](1).[cis-clomiphene] 0.48 -0.30 7.4 25.0 HPLC-method David S. Hage 1998
[b-Cyclodextrin](1).[trans-clomiphene] -0.52 -1.00 7.4 25.0 HPLC-method David S. Hage 1998
[b-Cyclodextrin](1).[phenylbutazone] 3.49 2.85 7.5 15.0 UV-vis spectroscopy David Diaz 1998
[b-Cyclodextrin](1).[phenylbutazone] 3.90 3.70 7.5 20.0 UV-vis spectroscopy David Diaz 1998
[b-Cyclodextrin](1).[phenylbutazone] 3.85 3.30 7.5 25.0 UV-vis spectroscopy David Diaz 1998
[b-Cyclodextrin](1).[phenylbutazone] 3.78 3.00 7.5 30.0 UV-vis spectroscopy David Diaz 1998
[b-Cyclodextrin](1).[phenylbutazone] 3.69 2.90 7.5 37.0 UV-vis spectroscopy David Diaz 1998
[b-Cyclodextrin](1).[phenylbutazone] 3.69 2.78 25.0 UV-vis spectroscopy David Diaz 1998
[b-Cyclodextrin](1).[phenylbutazone] 3.60 3.18 30.0 UV-vis spectroscopy David Diaz 1998
[b-Cyclodextrin](1).[phenylbutazone] 3.51 2.70 37.0 UV-vis spectroscopy David Diaz 1998
[b-Cyclodextrin](1).[phenylbutazone] 4.61 2.30 15.0 UV-vis spectroscopy David Diaz 1998
[b-Cyclodextrin](1).[phenylbutazone] 3.08 2.30 20.0 UV-vis spectroscopy David Diaz 1998
[b-Cyclodextrin](1).[oxyphenbutazone] 3.26 2.48 7.5 15.0 UV-vis spectroscopy David Diaz 1998
[b-Cyclodextrin](1).[oxyphenbutazone] 3.08 2.00 7.5 20.0 UV-vis spectroscopy David Diaz 1998
[b-Cyclodextrin](1).[oxyphenbutazone] 3.00 1.30 7.5 25.0 UV-vis spectroscopy David Diaz 1998
[b-Cyclodextrin](1).[oxyphenbutazone] 2.99 1.90 7.5 30.0 UV-vis spectroscopy David Diaz 1998
[b-Cyclodextrin](1).[oxyphenbutazone] 2.78 2.00 7.5 37.0 UV-vis spectroscopy David Diaz 1998
[b-Cyclodextrin](1).[oxyphenbutazone] 1.00 -0.40 15.0 UV-vis spectroscopy David Diaz 1998
[b-Cyclodextrin](1).[oxyphenbutazone] 1.41 20.0 UV-vis spectroscopy David Diaz 1998
[b-Cyclodextrin](1).[oxyphenbutazone] 1.76 0.48 25.0 UV-vis spectroscopy David Diaz 1998
[b-Cyclodextrin](1).[oxyphenbutazone] 1.79 0.48 30.0 UV-vis spectroscopy David Diaz 1998
[b-Cyclodextrin](1).[oxyphenbutazone] 1.74 0.48 37.0 UV-vis spectroscopy David Diaz 1998
[b-Cyclodextrin](1).[methylene blue] 3.65 7.2 25.0 UV-vis spectroscopy Hong-Yuan Chen 1999
[b-Cyclodextrin](1).[methylene blue] 3.65 7.2 25.0 Electrochemical method Hong-Yuan Chen 1999
[b-Cyclodextrin](1).[methylene blue] 3.64 7.2 20.0 Cyclic voltammetry Hong-Yuan Chen 1999
[b-Cyclodextrin](1).[methylene blue] 2.32 7.2 25.0 fluorescence spectroscopy Yu Liu 2002
[b-Cyclodextrin](1).[sodium a,w-hexyl dicarboxylate] 1.68 1.34 10.5 25.0 Apparent molar volume measurements Ronald E. Verrall 2000
[b-Cyclodextrin](1).[sodium a,w-octyl dicarboxylate] 2.71 2.20 10.5 25.0 Apparent molar volume measurements Ronald E. Verrall 2000
[b-Cyclodextrin](1).[sodium a,w-decanyl dicarboxylate] 3.27 2.74 10.5 25.0 Apparent molar volume measurements Ronald E. Verrall 2000
[b-Cyclodextrin](1).[sodium a,w-dodecyl dicarboxylate] 3.59 2.94 10.5 25.0 Apparent molar volume measurements Ronald E. Verrall 2000
[b-Cyclodextrin](1).[4,4'-azopyridine ligand] 2.64 2.04 7.0 25.0 UV-vis spectroscopy Donal H. Macartney 2000
[b-Cyclodextrin](1).[4,4'-azopyridine ligand] 2.49 1.48 7.0 25.0 NMR spectroscopy Donal H. Macartney 2000
[b-Cyclodextrin](1).[4-pyridinecarboxaldehyde azine] 2.21 1.56 7.0 25.0 UV-vis spectroscopy Donal H. Macartney 2000
[b-Cyclodextrin](1).[4-acetylpyridine azine] 2.51 1.61 7.0 25.0 UV-vis spectroscopy Donal H. Macartney 2000
[b-Cyclodextrin](1).[4-acetylpyridine azine] 2.75 1.78 7.0 25.0 NMR spectroscopy Donal H. Macartney 2000
[b-Cyclodextrin](1).[[(NC)5Fe(bpe)Fe(CN)5]6-] 2.32 1.64 7.0 25.0 UV-vis spectroscopy Donal H. Macartney 2000
[b-Cyclodextrin](1).[[(NC)5Fe(bpe)Fe(CN)5]6-] 2.45 1.54 7.0 25.0 NMR spectroscopy Donal H. Macartney 2000
[b-Cyclodextrin](1).[[(NC)5Fe(azp)Fe(CN)5]6-] 2.16 1.70 7.0 25.0 UV-vis spectroscopy Donal H. Macartney 2000
[b-Cyclodextrin](1).[[(NC)5Fe(pca)Fe(CN)5]6-] 2.45 1.81 7.0 25.0 UV-vis spectroscopy Donal H. Macartney 2000
[b-Cyclodextrin](1).[[(NC)5Fe(apa)Fe(CN)5]6-] 2.90 2.34 7.0 25.0 UV-vis spectroscopy Donal H. Macartney 2000
[b-Cyclodextrin](1).[neutral red] 1.88 5.0 20.0 Fluorescence spectroscopy Shaomin Shuang 2002
[b-Cyclodextrin](1).[neutral red] 2.74 7.5 20.0 Fluorescence spectroscopy Shaomin Shuang 2002
[b-Cyclodextrin](1).[neutral red] 2.83 10.5 20.0 Fluorescence spectroscopy Shaomin Shuang 2002
[b-Cyclodextrin](1).[neutral red] 2.24 6.6 25.0 UV/VIS spectrometry Abbas Afkhami 2006
[b-Cyclodextrin](1).[neutral red] 2.68 7.2 25.0 Fluorescence spectroscopy Yu Liu 2003
[b-Cyclodextrin](1).[neutral red] 2.61 1.40 9.0 25.0 Fluorescence spectroscopy M. K. Singh 2004
[b-Cyclodextrin](1).[neutral red] 2.68 7.2 25.0 UV-vis spectroscopy Yu Liu 2003
[b-Cyclodextrin](1).[neutral red] 2.68 7.2 25.0 fluorescence spectroscopy Yu Liu 2002
[b-Cyclodextrin](1).[p-amino-nitrobenzene] 2.58 1.60 6.0 25.0 UV-vis spectroscopy Renato Noto 2002
[b-Cyclodextrin](1).[p-amino-nitrobenzene] 2.54 1.48 8.0 25.0 UV-vis spectroscopy Renato Noto 2002
[b-Cyclodextrin](1).[p-amino-nitrobenzene] 2.53 1.48 11.0 25.0 UV-vis spectroscopy Renato Noto 2002
[b-Cyclodextrin](1).[p-aminomethyl-nitrobenzene] 3.03 1.90 6.0 25.0 UV-vis spectroscopy Renato Noto 2002
[b-Cyclodextrin](1).[p-aminomethyl-nitrobenzene] 2.90 1.90 8.0 25.0 UV-vis spectroscopy Renato Noto 2002
[b-Cyclodextrin](1).[p-aminomethyl-nitrobenzene] 2.75 1.78 11.0 25.0 UV-vis spectroscopy Renato Noto 2002
[b-Cyclodextrin](1).[p-dimethylamino-nitrobenzene] 2.85 1.70 6.0 25.0 UV-vis spectroscopy Renato Noto 2002
[b-Cyclodextrin](1).[p-dimethylamino-nitrobenzene] 2.82 1.85 8.0 25.0 UV-vis spectroscopy Renato Noto 2002
[b-Cyclodextrin](1).[p-dimethylamino-nitrobenzene] 2.76 1.60 11.0 25.0 UV-vis spectroscopy Renato Noto 2002
[b-Cyclodextrin](1).[p-ethyl-nitrobenzene] 2.60 2.20 6.0 25.0 UV-vis spectroscopy Renato Noto 2002
[b-Cyclodextrin](1).[p-ethyl-nitrobenzene] 2.38 1.60 8.0 25.0 UV-vis spectroscopy Renato Noto 2002
[b-Cyclodextrin](1).[p-ethyl-nitrobenzene] 2.60 2.20 11.0 25.0 UV-vis spectroscopy Renato Noto 2002
[b-Cyclodextrin](1).[p-isopropyl-nitrobenzene] 3.16 1.81 6.0 25.0 UV-vis spectroscopy Renato Noto 2002
[b-Cyclodextrin](1).[p-isopropyl-nitrobenzene] 3.04 2.40 8.0 25.0 UV-vis spectroscopy Renato Noto 2002
[b-Cyclodextrin](1).[p-isopropyl-nitrobenzene] 3.04 2.11 11.0 25.0 UV-vis spectroscopy Renato Noto 2002
[b-Cyclodextrin](1).[p-methxy-nitrobenzene] 2.24 1.48 6.0 25.0 UV-vis spectroscopy Renato Noto 2002
[b-Cyclodextrin](1).[p-methxy-nitrobenzene] 2.31 1.78 8.0 25.0 UV-vis spectroscopy Renato Noto 2002
[b-Cyclodextrin](1).[p-methxy-nitrobenzene] 2.23 1.30 11.0 25.0 UV-vis spectroscopy Renato Noto 2002
[b-Cyclodextrin](1).[20(S)-Camptothecin] 2.42 1.7 25.0 HPLC-method Vijay Kumar 2002
[b-Cyclodextrin](1).[acridine red] 3.42 7.2 25.0 Fluorescence spectroscopy Yu Liu 2003
[b-Cyclodextrin](1).[acridine red] 3.49 7.0 25.0 Fluorescence spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[acridine red] 3.32 7.2 25.0 UV-vis spectroscopy Yu Liu 2003
[b-Cyclodextrin](1).[acridine red] 3.14 6.0 25.0 Fluorescence spectroscopy Yu Liu 2002
[b-Cyclodextrin](1).[acridine red] 0.50 7.2 30.0 Fluorescence spectroscopy Yu Liu 2002
[b-Cyclodextrin](1).[acridine red] 0.49 7.2 35.0 Fluorescence spectroscopy Yu Liu 2002
[b-Cyclodextrin](1).[acridine red] 0.47 7.2 40.0 Fluorescence spectroscopy Yu Liu 2002
[b-Cyclodextrin](1).[acridine red] 3.42 7.2 25.0 fluorescence spectroscopy Yu Liu 2002
[b-Cyclodextrin](1).[rhodamine B] 3.63 7.2 25.0 Fluorescence spectroscopy Yu Liu 2003
[b-Cyclodextrin](1).[rhodamine B] 3.69 7.0 25.0 Fluorescence spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[rhodamine B] 3.63 7.2 25.0 UV-vis spectroscopy Yu Liu 2003
[b-Cyclodextrin](1).[rhodamine B] 0.63 7.2 30.0 Fluorescence spectroscopy Yu Liu 2002
[b-Cyclodextrin](1).[rhodamine B] 0.67 7.2 35.0 Fluorescence spectroscopy Yu Liu 2002
[b-Cyclodextrin](1).[rhodamine B] 0.70 7.2 40.0 Fluorescence spectroscopy Yu Liu 2002
[b-Cyclodextrin](1).[brilliant green] 3.34 7.2 25.0 Fluorescence spectroscopy Yu Liu 2003
[b-Cyclodextrin](1).[brilliant green] 3.34 7.2 25.0 UV-vis spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[brilliant green] 3.34 25.0 UV-vis spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[polygodial] 3.00 7.0 37.0 UV-vis spectroscopy Rosendo A. Yunes 2003
[b-Cyclodextrin](1).[hesperetin] 2.79 7.0 15.0 UV-vis spectroscopy Maria Luisa Calabrò 2004
[b-Cyclodextrin](1).[hesperetin] 2.37 7.0 25.0 UV-vis spectroscopy Maria Luisa Calabrò 2004
[b-Cyclodextrin](1).[hesperetin] 2.36 7.0 35.0 UV-vis spectroscopy Maria Luisa Calabrò 2004
[b-Cyclodextrin](1).[hesperetin] 2.11 7.0 45.0 UV-vis spectroscopy Maria Luisa Calabrò 2004
[b-Cyclodextrin](1).[naringenin] 2.85 7.0 15.0 UV-vis spectroscopy Maria Luisa Calabrò 2004
[b-Cyclodextrin](1).[naringenin] 2.55 7.0 25.0 UV-vis spectroscopy Maria Luisa Calabrò 2004
[b-Cyclodextrin](1).[naringenin] 2.26 7.0 35.0 UV-vis spectroscopy Maria Luisa Calabrò 2004
[b-Cyclodextrin](1).[naringenin] 1.98 7.0 45.0 UV-vis spectroscopy Maria Luisa Calabrò 2004
[b-Cyclodextrin](1).[naringenin] 2.58 4.0 25.0 UV-vis spectroscopy M. L. Calabro 2004
[b-Cyclodextrin](1).[naringenin] 1.28 8.0 25.0 UV-vis spectroscopy M. L. Calabro 2004
[b-Cyclodextrin](1).[3-hydroxyflavone] 2.98 7.0 25.0 UV-vis spectroscopy S. Tommasini 2004
[b-Cyclodextrin](1).[morin] 2.52 7.0 25.0 UV-vis spectroscopy S. Tommasini 2004
[b-Cyclodextrin](1).[quercetin] 2.11 7.0 25.0 UV-vis spectroscopy S. Tommasini 2004
[b-Cyclodextrin](1).[quercetin] 3.06 1.72 7.0 25.0 Fluorescence Spectroscopy and Ferric Reducing/Antioxidant Power Assay (FRAP) techniques Emilio Alvarez-Parrilla 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinones] 2.78 1.70 1.0 25.0 UV-vis spectroscopy Jean-Louis Montero 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinones] 2.79 1.60 4.3 25.0 UV-vis spectroscopy Jean-Louis Montero 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinones] 4.04 1.90 7.4 25.0 UV-vis spectroscopy Jean-Louis Montero 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinones] 4.04 1.00 8.5 25.0 UV-vis spectroscopy Jean-Louis Montero 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinones] 3.98 1.85 11.0 25.0 UV-vis spectroscopy Jean-Louis Montero 2005
[b-Cyclodextrin](1).[o-dihydroxy benzene] 2.59 7.0 27.0 Fluorescence spectroscopy N. Rajendiran 2005
[b-Cyclodextrin](1).[m-dihydroxy benzene] 2.45 7.0 27.0 Fluorescence spectroscopy N. Rajendiran 2005
[b-Cyclodextrin](1).[p-dihydroxy benzene] 2.31 7.0 27.0 Fluorescence spectroscopy N. Rajendiran 2005
[b-Cyclodextrin](1).[4-hydroxy-3,5-dimethoxybenzaldehyde] 2.24 7.0 30.0 UV-vis spectroscopy N. Rajendiran 2005
[b-Cyclodextrin](1).[4-hydroxy-3,5-dimethoxybenzaldehyde] 1.97 7.0 30.0 Fluorescence spectroscopy N. Rajendiran 2005
[b-Cyclodextrin](1).[tyrosine] 1.70 0.60 6.0 20.0 Fluorescence spectroscopy Wieslaw Wiczk 2005
[b-Cyclodextrin](1).[N-acetyltyrosine] 2.20 1.25 6.0 20.0 Fluorescence spectroscopy Wieslaw Wiczk 2005
[b-Cyclodextrin](1).[O-methyl tyrosine] 1.30 1.15 6.0 20.0 Fluorescence spectroscopy Wieslaw Wiczk 2005
[b-Cyclodextrin](1).[O-methyl-b-tyrosine] 1.28 0.78 6.0 20.0 Fluorescence spectroscopy Wieslaw Wiczk 2005
[b-Cyclodextrin](1).[b-homotyrosine] 2.14 1.76 6.0 20.0 Fluorescence spectroscopy Wieslaw Wiczk 2005
[b-Cyclodextrin](1).[b-homotyrosine] 1.92 0.76 6.0 25.0 Calorimetry Wieslaw Wiczk 2005
[b-Cyclodextrin](1).[O-methyl-b-homotyrosine] 2.06 1.60 6.0 20.0 Fluorescence spectroscopy Wieslaw Wiczk 2005
[b-Cyclodextrin](1).[O-methyl-b-homotyrosine] 2.14 1.08 6.0 25.0 Calorimetry Wieslaw Wiczk 2005
[b-Cyclodextrin](1).[tyramine hydrochloride] 1.65 1.04 6.0 20.0 Fluorescence spectroscopy Wieslaw Wiczk 2005
[b-Cyclodextrin](1).[3-(4-hydroxyphenyl)-propionic acid] 2.84 1.34 2.0 20.0 Fluorescence spectroscopy Wieslaw Wiczk 2005
[b-Cyclodextrin](1).[3-(4-hydroxyphenyl)-propionic acid] 2.45 1.45 8.0 20.0 Fluorescence spectroscopy Wieslaw Wiczk 2005
[b-Cyclodextrin](1).[4-ethyl-phenol] 2.81 1.45 6.0 20.0 Fluorescence spectroscopy Wieslaw Wiczk 2005
[b-Cyclodextrin](1).[4-ethyl-phenol] 2.66 0.95 6.0 25.0 Calorimetry Wieslaw Wiczk 2005
[b-Cyclodextrin](1).[homo-phenylalanine] 1.91 0.95 6.0 20.0 Fluorescence spectroscopy Wieslaw Wiczk 2005
[b-Cyclodextrin](1).[phenylalanine] 1.02 0.79 6.0 20.0 Fluorescence spectroscopy Wieslaw Wiczk 2005
[b-Cyclodextrin](1).[phenylalanine] 1.84 0.85 7.0 30.0 NMR spectroscopy Akira Harada 2006
[b-Cyclodextrin](1).[b-phenylalanine] 1.51 0.88 6.0 20.0 Fluorescence spectroscopy Wieslaw Wiczk 2005
[b-Cyclodextrin](1).[Ro 28-2653] 3.32 7.0 37.0 HPLC-method Bertholet Pascal 2005
[b-Cyclodextrin](1).[proflavin] 2.74 1.78 1.8 UV-vis spectroscopy Itamar Willner 1989
[b-Cyclodextrin](1).[pyrene] 5.93 Fluorescence spectroscopy Isiah M. Warner 1991
[b-Cyclodextrin](1).[pyrene] 1.64 0.82 7.0 21.0 Fluorescence spectroscopy J. K. Thomas 1985
[b-Cyclodextrin](1).[pyrene] 2.15 7.0 25.0 Fluorescence spectroscopy J. N. Demas 1993
[b-Cyclodextrin](1).[pyrene] 2.63 2.11 6.7 20.0 Fluorescence spectroscopy Cornelia Bohne 1996
[b-Cyclodextrin](2).[pyrene] 3.15 2.60 6.7 20.0 Fluorescence spectroscopy Cornelia Bohne 1996
[b-Cyclodextrin](1).[naphtalene] 2.93 1.95 7.0 21.0 Fluorescence spectroscopy J. K. Thomas 1985
[b-Cyclodextrin](1).[naphtalene] 2.84 J. K. Thomas 1985
[b-Cyclodextrin](1).[naphtalene] 2.67 7.0 22.0 UV/VIS spectrometry Khalil Hanna 2004
[b-Cyclodextrin](2).[naphtalene] 3.60 J. K. Thomas 1985
[b-Cyclodextrin](1).[DNP-L-valine ] 3.25 2.00 6.0 25.0 UV-vis spectroscopy William C. Purdy 1992
[b-Cyclodextrin](1).[DNP-L-valine ] 3.45 1.70 6.0 21.0 Circular dichroism spectroscopy William C. Purdy 1992
[b-Cyclodextrin](1).[DNP-L-valine ] 3.45 11.0 20.0 NMR spectroscopy William C. Purdy 1992
[b-Cyclodextrin](1).[DNP-D-valine ] 3.37 2.23 6.0 25.0 UV-vis spectroscopy William C. Purdy 1992
[b-Cyclodextrin](1).[DNP-D-valine ] 3.51 1.70 6.0 21.0 Circular dichroism spectroscopy William C. Purdy 1992
[b-Cyclodextrin](1).[DNP-D-valine ] 3.53 11.0 20.0 NMR spectroscopy William C. Purdy 1992
[b-Cyclodextrin](1).[DNP-L-leucine ] 4.85 3.61 6.0 25.0 UV-vis spectroscopy William C. Purdy 1992
[b-Cyclodextrin](1).[DNP-L-leucine ] 3.22 2.30 6.0 21.0 Circular dichroism spectroscopy William C. Purdy 1992
[b-Cyclodextrin](1).[DNP-L-leucine ] 3.18 11.0 20.0 NMR spectroscopy William C. Purdy 1992
[b-Cyclodextrin](1).[DNP-D-leucine ] 3.06 2.32 6.0 25.0 UV-vis spectroscopy William C. Purdy 1992
[b-Cyclodextrin](1).[DNP-D-leucine ] 3.33 2.40 6.0 21.0 Circular dichroism spectroscopy William C. Purdy 1992
[b-Cyclodextrin](1).[DNP-D-leucine ] 3.39 11.0 20.0 NMR spectroscopy William C. Purdy 1992
[b-Cyclodextrin](1).[DNP-L-methionine ] 3.14 2.28 6.0 25.0 UV-vis spectroscopy William C. Purdy 1992
[b-Cyclodextrin](1).[DNP-L-methionine ] 3.12 1.85 6.0 21.0 Circular dichroism spectroscopy William C. Purdy 1992
[b-Cyclodextrin](1).[DNP-L-methionine ] 3.39 11.0 20.0 NMR spectroscopy William C. Purdy 1992
[b-Cyclodextrin](1).[DNP-D-methionine] 3.25 2.40 6.0 25.0 UV-vis spectroscopy William C. Purdy 1992
[b-Cyclodextrin](1).[DNP-D-methionine] 3.33 2.61 6.0 21.0 Circular dichroism spectroscopy William C. Purdy 1992
[b-Cyclodextrin](1).[DNP-D-methionine] 3.47 11.0 20.0 NMR spectroscopy William C. Purdy 1992
[b-Cyclodextrin](1).[n-BuSO3-] 1.05 -0.42 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[b-Cyclodextrin](1).[n-PrCO2-] 0.59 -1.22 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[b-Cyclodextrin](1).[n-BuCO2-] 1.13 0.04 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[b-Cyclodextrin](1).[n-PenCO2-] 1.80 0.59 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[b-Cyclodextrin](1).[c-HexCO2-] 1.83 0.27 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[b-Cyclodextrin](1).[n-HexCO2-] 2.23 0.76 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[b-Cyclodextrin](1).[n-HepCO2-] 1.25 -0.50 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[b-Cyclodextrin](1).[n-HexOH] 2.36 0.71 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[b-Cyclodextrin](1).[c-HexOH] 2.74 1.79 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[b-Cyclodextrin](1).[HO(CH2)6OH] 1.54 0.77 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[b-Cyclodextrin](1).[I-] 0.67 -1.36 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[b-Cyclodextrin](1).[Br-] 0.22 -2.26 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[b-Cyclodextrin](1).[Br-] -0.09 7.0 50.0 NMR spectroscopy Jose J. C. Teixeira-Dias 2004
[b-Cyclodextrin](1).[ClO4-] 1.14 0.18 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[b-Cyclodextrin](1).[ClO4-] 0.31 7.0 50.0 NMR spectroscopy Jose J. C. Teixeira-Dias 2004
[b-Cyclodextrin](1).[4-nitrocatechol] 2.38 6.3 25.0 UV/VIS spectrometry Abbas Afkhami 2006
[b-Cyclodextrin](1).[Polyethylene glycol (n = 9.5) n-octylphenyl ether] 4.42 3.23 7.0 25.0 Fluorescence and phosporescence spectroscopy Xinzhen Du 2005
[b-Cyclodextrin](1).[ 4,4'-bipyridine] 2.23 1.32 7.0 25.0 NMR spectroscopy Dona1 H. Macartney 1993
[b-Cyclodextrin](1).[ 4,4'-bipyridine] 2.14 7.2 25.0 Circular dichroism spectroscopy Keith 0. Hodgson 1979
[b-Cyclodextrin](1).[trons-1,2-bis(4-pyridyl)ethylene] 2.38 1.57 7.0 25.0 NMR spectroscopy Dona1 H. Macartney 1993
[b-Cyclodextrin](1).[1,2-bis(4-pyridyl)ethane] 2.92 1.91 7.0 25.0 NMR spectroscopy Dona1 H. Macartney 1993
[b-Cyclodextrin](1).[1,3-bis(4-pyridyl)propane] 3.49 3.23 7.0 25.0 NMR spectroscopy Dona1 H. Macartney 1993
[b-Cyclodextrin](2).[1,3-bis(4-pyridyl)propane] 1.48 1.87 7.0 25.0 NMR spectroscopy Dona1 H. Macartney 1993
[b-Cyclodextrin](1).[4-tert-butylpyridine] 3.87 3.04 7.0 25.0 NMR spectroscopy Dona1 H. Macartney 1993
[b-Cyclodextrin](1).[3-phenylpyridine] 3.20 2.59 7.0 25.0 NMR spectroscopy Dona1 H. Macartney 1993
[b-Cyclodextrin](1).[4-phenylpyridine] 3.32 2.41 7.0 25.0 NMR spectroscopy Dona1 H. Macartney 1993
[b-Cyclodextrin](1).[4-benzylpyridine] 3.55 2.91 7.0 25.0 NMR spectroscopy Dona1 H. Macartney 1993
[b-Cyclodextrin](1).[4-phenylpyrimidine] 2.43 1.78 7.0 25.0 NMR spectroscopy Dona1 H. Macartney 1993
[b-Cyclodextrin](1).[polyethylene glycol (n = 10) tert-octylphenyl ether] 4.48 3.34 7.0 25.0 Fluorescence and phosporescence spectroscopy Xinzhen Du 2005
[b-Cyclodextrin](1).[[Fe(CN)5(4-phpyr)]] 3.28 2.70 7.0 25.0 UV-vis spectroscopy Dona1 H. Macartney 1993
[b-Cyclodextrin](1).[[Fe(CN)5(4-phpyr)]] 3.30 2.60 7.0 25.0 NMR spectroscopy Dona1 H. Macartney 1993
[b-Cyclodextrin](1).[[Fe(CN)5(4-bzpyr)]] 3.26 2.60 7.0 25.0 UV-vis spectroscopy Dona1 H. Macartney 1993
[b-Cyclodextrin](1).[[Fe(CN)5(4-bzpyr)]] 3.24 2.99 7.0 25.0 NMR spectroscopy Dona1 H. Macartney 1993
[b-Cyclodextrin](1).[[Fe(CN)5(4-t-bupyr)]] 3.66 3.00 7.0 25.0 UV-vis spectroscopy Dona1 H. Macartney 1993
[b-Cyclodextrin](1).[[Fe(CN)5(4-t-bupyr)]] 3.79 2.95 7.0 25.0 NMR spectroscopy Dona1 H. Macartney 1993
[b-Cyclodextrin](1).[1-naphthalenesulfonate] 3.40 0.06 7.2 25.0 Calorimetry Yoshihisa Inoue 1993
[b-Cyclodextrin](1).[2-naphthalenesul fonate] 5.37 0.07 7.2 25.0 Calorimetry Yoshihisa Inoue 1993
[b-Cyclodextrin](1).[2,6-naphthalenedisulfonate] 3.29 0.05 7.2 25.0 Calorimetry Yoshihisa Inoue 1993
[b-Cyclodextrin](1).[2,7-naphthalenedisulfonate ] 2.44 0.02 7.2 25.0 Calorimetry Yoshihisa Inoue 1993
[b-Cyclodextrin](1).[2,3,6-naphthalenetrisulfonate ] 2.22 0.03 7.2 25.0 Calorimetry Yoshihisa Inoue 1993
[b-Cyclodextrin](1).[4-amino-1-naphthalenesulfonate] 1.70 0.03 7.2 25.0 Calorimetry Yoshihisa Inoue 1993
[b-Cyclodextrin](1).[1-naphthaleneacetate] 4.35 0.05 7.2 25.0 Calorimetry Yoshihisa Inoue 1993
[b-Cyclodextrin](1).[cyclohexnol] 2.60 7.2 25.0 Circular dichroism spectroscopy Keith 0. Hodgson 1979
[b-Cyclodextrin](1).[methoxybenzene] 1.72 7.2 25.0 Circular dichroism spectroscopy Keith 0. Hodgson 1979
[b-Cyclodextrin](1).[toluene] 0.82 7.2 25.0 Circular dichroism spectroscopy Keith 0. Hodgson 1979
[b-Cyclodextrin](1).[toluene] 2.24 0.60 25.0 GC (SHSGC) É. Fenyvesi 2005
[b-Cyclodextrin](1).[nerol] 2.77 7.2 25.0 Circular dichroism spectroscopy Keith 0. Hodgson 1979
[b-Cyclodextrin](1).[geraniol] 2.82 7.2 25.0 Circular dichroism spectroscopy Keith 0. Hodgson 1979
[b-Cyclodextrin](1).[p-nitrophenyl a-D-mannose] 2.42 7.0 30.0 NMR spectroscopy Soledad Penades 1993
[b-Cyclodextrin](1).[p-nitrophenyl b-D-mannose] 2.27 7.0 30.0 NMR spectroscopy Soledad Penades 1993
[b-Cyclodextrin](1).[risperidone] 2.05 2.0 25.0 UV-Vis spectroscopy M.B. Zughul 2005
[b-Cyclodextrin](1).[risperidone] 2.97 5.65 25.0 UV-Vis spectroscopy M.B. Zughul 2005
[b-Cyclodextrin](1).[risperidone] 3.39 10.5 25.0 UV-Vis spectroscopy M.B. Zughul 2005
[b-Cyclodextrin](1).[risperidone] 2.64 12.4 25.0 UV-Vis spectroscopy M.B. Zughul 2005
[b-Cyclodextrin](2).[risperidone] 1.72 10.5 25.0 UV-Vis spectroscopy M.B. Zughul 2005
[b-Cyclodextrin](2).[risperidone] 2.00 12.4 25.0 UV-Vis spectroscopy M.B. Zughul 2005
[b-Cyclodextrin](1).[vanillin] 4.05 3.26 7.0 20.0 NMR spectroscopy Soundar Divakar 1990
[b-Cyclodextrin](1).[9-methylanthracene] 2.45 1.60 25.0 Fluorescence spectroscopy Vincent C. Reinsborough 1995
[b-Cyclodextrin](2).[manganese(III) tetrakis(4-sulfonatopheny1)porphine] 1.97 7.0 25.0 UV-vis spectroscopy Robert G. Bryant 1995
[b-Cyclodextrin](2).[tetrakis(4-sulfonatopheny1)porphine] 2.64 7.0 25.0 UV-vis spectroscopy Robert G. Bryant 1995
[b-Cyclodextrin](1).[porphyrin] 3.15 7.0 25.0 Fluorescence spectroscopy Roeland J. M. Nolte 1996
[b-Cyclodextrin](1).[steroid] 6.07 5.00 9.0 25.0 Titration Calorimetry Ronald Breslow 1997
[b-Cyclodextrin](1).[2-anilinonaphthalene-6-sulfonic acid] 3.33 1.78 7.0 19.0 High-pressure fluorescence spectroscopy Christine E. Evans 1997
[b-Cyclodextrin](1).[2-(N-methylanilino)naphthalene-6-sulfonic acid sodium salt] 4.22 2.48 7.0 19.0 High-pressure fluorescence spectroscopy Christine E. Evans 1997
[b-Cyclodextrin](1).[ferrocene derivative ] 3.33 2.40 8.6 25.0 Calorimetry Cecil M. Criss 1997
[b-Cyclodextrin](1).[naphtalene derivative] 2.51 1.30 8.6 25.0 Calorimetry Cecil M. Criss 1997
[b-Cyclodextrin](1).[adamantane derivative] 4.02 3.13 8.6 25.0 Calorimetry Cecil M. Criss 1997
[b-Cyclodextrin](1).[2-(4'-aminophenyl)benzothiazole] 3.19 7.0 25.0 Fluorescence spectroscopy Isiah M. Warner 1998
[b-Cyclodextrin](1).[4-nitrophenol] 2.55 6.6 25.0 UV/VIS spectrometry Abbas Afkhami 2006
[b-Cyclodextrin](1).[4-nitrophenol] 2.10 5.0 25.0 Capillary electrophoresis Thomas Le Saux 2006
[b-Cyclodextrin](1).[4-nitrophenol] 2.20 5.0 25.0 Microchip electrophoresis Thomas Le Saux 2006
[b-Cyclodextrin](1).[4-nitrophenol] 2.34 1.70 3.5 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[b-Cyclodextrin](2).[2-aminodiphenylsulphone] 5.10 6.0 25.0 UV-Vis spectroscopy and fluorescence spectroscopy Meenakshisundaram Swaminathan 2005
[b-Cyclodextrin](1).[2-(4'-(N,N-dimethylamino)phenyl)benzothiazole] 3.74 7.0 25.0 Fluorescence spectroscopy Isiah M. Warner 1998
[b-Cyclodextrin](3).[iodotrimethyl 2-(p-hexylaminophenyl)-3,3-dimethyl-5-carboethoxy-3H-indole ammonium] 5.57 4.60 9.5 25.0 Fluorescence spectroscopy Gilles Durocher 1998
[b-Cyclodextrin](1).[16-methylene-17a-acetoxy-19-norpregn-4-ene-3,20-dione] 3.64 2.44 7.4 30.0 UV-vis spectroscopy Sayed M. Ahmed 1998
[b-Cyclodextrin](1).[16-methylene-17a-acetoxy-19-norpregn-4-ene-3,20-dione] 3.47 2.36 7.4 37.0 UV-vis spectroscopy Sayed M. Ahmed 1998
[b-Cyclodextrin](1).[16-methylene-17a-acetoxy-19-norpregn-4-ene-3,20-dione] 3.19 1.95 7.4 45.0 UV-vis spectroscopy Sayed M. Ahmed 1998
[b-Cyclodextrin](1).[econazole nitrate] 2.92 0.18 30.0 PH metric titration Moustafa M.G. Fouda 2006
[b-Cyclodextrin](2).[ciclopirox olamine] 2.09 0.06 30.0 PH metric titration Moustafa M.G. Fouda 2006
[b-Cyclodextrin](1).[glisentide] 2.82 1.48 4.2 15.0 UV-vis spectroscopy A. Zornoza 1998
[b-Cyclodextrin](1).[glisentide] 2.76 1.60 4.2 20.0 UV-vis spectroscopy A. Zornoza 1998
[b-Cyclodextrin](1).[glisentide] 2.71 1.30 4.2 25.0 UV-vis spectroscopy A. Zornoza 1998
[b-Cyclodextrin](1).[glisentide] 2.66 1.30 4.2 30.0 UV-vis spectroscopy A. Zornoza 1998
[b-Cyclodextrin](1).[glisentide] 2.59 1.00 4.2 37.0 UV-vis spectroscopy A. Zornoza 1998
[b-Cyclodextrin](1).[glisentide] 1.90 0.60 8.6 25.0 UV-vis spectroscopy A. Zornoza 1998
[b-Cyclodextrin](1).[(-)-N-(benzo[b]thien-2-ylethyl) N-hydroxyurea] 3.74 2.87 7.0 25.0 NMR spectroscopy M. Cotta Ramusino 1998
[b-Cyclodextrin](1).[(-)-N-(benzo[b]thien-2-ylethyl) N-hydroxyurea] 3.77 2.87 7.0 25.0 UV-vis spectroscopy M. Cotta Ramusino 1998
[b-Cyclodextrin](1).[(-)-N-(benzo[b]thien-2-ylethyl) N-hydroxyurea] 3.71 2.26 7.0 25.0 Circular dichroism spectroscopy M. Cotta Ramusino 1998
[b-Cyclodextrin](1).[chlorpromazine hydrochloride] 3.79 7.4 37.0 Surface tension Noriaki Funasaki 1999
[b-Cyclodextrin](1).[chlorpromazine hydrochloride] 4.08 25.0 UV-vis spectroscopy Noriaki Funasaki 1999
[b-Cyclodextrin](1).[chlorpromazine hydrochloride] 3.90 25.0 Circular dichroism spectroscopy Noriaki Funasaki 1999
[b-Cyclodextrin](1).[propantheline bromide] 3.53 37.0 Surface tension Noriaki Funasaki 1999
[b-Cyclodextrin](2).[propantheline bromide] 3.08 37.0 Surface tension Noriaki Funasaki 1999
[b-Cyclodextrin](1).[indomethacin] 2.49 1.48 10.0 40.0 HPLC-method Thorsteinn Loftsson 1999
[b-Cyclodextrin](1).[indomethacin] 2.76 1.6 37.0 UV spectroscopy, induced circular dichroism Dominique Duchene 1998
[b-Cyclodextrin](1).[indomethacin] 2.83 6.8 37.0 UV spectroscopy, induced circular dichroism Dominique Duchene 1998
[b-Cyclodextrin](1).[chlorambucil] 3.73 2.04 7.5 30.0 HPLC-method Thorsteinn Loftsson 1999
[b-Cyclodextrin](1).[TX100] 4.50 5.0 25.0 Calorimetric titrations H.-J. Buschmann 2000
[b-Cyclodextrin](1).[Benzyl tert-butyl nitroxide] 3.11 7.0 21.0 EPR spectroscopy Marco Lucarini 2004
[b-Cyclodextrin](1).[NP10 ] 4.74 5.0 25.0 Calorimetric titrations H.-J. Buschmann 2000
[b-Cyclodextrin](1).[NP20 ] 4.96 5.0 25.0 Calorimetric titrations H.-J. Buschmann 2000
[b-Cyclodextrin](1).[Igepal CO-720 ] 4.91 5.0 25.0 Calorimetric titrations H.-J. Buschmann 2000
[b-Cyclodextrin](1).[Brij30 ] 3.23 5.0 25.0 Calorimetric titrations H.-J. Buschmann 2000
[b-Cyclodextrin](1).[Brij56 ] 5.00 5.0 25.0 Calorimetric titrations H.-J. Buschmann 2000
[b-Cyclodextrin](1).[Brij99 ] 5.00 5.0 25.0 Calorimetric titrations H.-J. Buschmann 2000
[b-Cyclodextrin](1).[PEG1000 ] 3.17 5.0 25.0 Calorimetric titrations H.-J. Buschmann 2000
[b-Cyclodextrin](1).[dibenzyl nitroxide] 2.59 7.0 21.0 EPR spectroscopy Marco Lucarini 2004
[b-Cyclodextrin](2).[dibenzyl nitroxide] 1.51 7.0 21.0 EPR spectroscopy Marco Lucarini 2004
[b-Cyclodextrin](1).[di-tert amyl nitroxide] 3.04 7.0 21.0 EPR spectroscopy Marco Lucarini 2004
[b-Cyclodextrin](2).[di-tert amyl nitroxide] 1.75 7.0 21.0 EPR spectroscopy Marco Lucarini 2004
[b-Cyclodextrin](1).[Fe(III)-tetrakis(sulfonatophenyl)porphyrin] 1.54 0.07 6.0 25.0 UV-Vis spectroscopy Masami Fukushima 2006
[b-Cyclodextrin](1).[p-N,Ndimethylaminobenzoic acid] 2.17 7.0 Fluorescence spectroscopy Minjoong Yoon 2001
[b-Cyclodextrin](0.5).[thymol] 2.68 1.60 7.0 20.0 UV-vis spectroscopy Soundar Divakar 2001
[b-Cyclodextrin](1).[pancreatic a-amylase] 2.89 6.9 30.0 UV-vis spectroscopy Roger Koukiekolo 2001
[b-Cyclodextrin](1).[tetrakis(sulfonatophenyl)porphyrin] 1.45 0.14 6.0 25.0 UV-Vis spectroscopy Masami Fukushima 2006
[b-Cyclodextrin](1).[2,3-naphthalenedicarboxylic acid, 1,4-dihydroxy-diethyl ester] 2.75 1.36 1.6 20.0 Fluorescence spectroscopy Bo Tang 2002
[b-Cyclodextrin](1).[2,3-naphthalenedicarboxylic acid, 1,4-dihydroxy-diethyl ester] 2.84 1.6 10.0 Fluorescence spectroscopy Bo Tang 2002
[b-Cyclodextrin](1).[2,3-naphthalenedicarboxylic acid, 1,4-dihydroxy-diethyl ester] 2.65 1.6 30.0 Fluorescence spectroscopy Bo Tang 2002
[b-Cyclodextrin](1).[2,3-naphthalenedicarboxylic acid, 1,4-dihydroxy-diethyl ester] 2.53 1.6 40.0 Fluorescence spectroscopy Bo Tang 2002
[b-Cyclodextrin](1).[2,3-naphthalenedicarboxylic acid, 1,4-dihydroxy-diethyl ester] 2.42 1.6 50.0 Fluorescence spectroscopy Bo Tang 2002
[b-Cyclodextrin](1).[cyclohexanol-d12 ] 2.85 0.78 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(R)-camphanic acid] 2.25 0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(R)-camphor sulfonic acid ] 2.75 1.00 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[4-phenylbutylamine ] 2.61 0.78 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[4-toluic acid ] 1.98 0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[3-(2-hydroxyphenyl)propionic acid ] 1.91 0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[3-(4-hydroxyphenyl)propionic acid ] 2.47 0.60 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[2-phenylethylamine ] 1.38 0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[tyramine ] 1.85 0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[N-acetyl-L-phenylalanine-d8 ] 1.83 0.15 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(R)-hexahydromandelic acid] 2.81 1.08 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(R)1-cyclohexylethylamine ] 2.52 0.48 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[adenine] 2.03 7.0 Fluorescence spectroscopy Xu Hao 2002
[b-Cyclodextrin](2).[curcumin] 5.74 2.4 20.0 UV-vis spectroscopy Bo Tang 2002
[b-Cyclodextrin](2).[curcumin] 5.51 2.4 35.0 UV-vis spectroscopy Bo Tang 2002
[b-Cyclodextrin](2).[curcumin] 5.40 2.4 45.0 UV-vis spectroscopy Bo Tang 2002
[b-Cyclodextrin](2).[curcumin] 5.22 2.4 55.0 UV-vis spectroscopy Bo Tang 2002
[b-Cyclodextrin](2).[curcumin] 5.07 2.4 65.0 UV-vis spectroscopy Bo Tang 2002
[b-Cyclodextrin](1).[N-acetyl-D-tryptophan ] 1.10 -0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[N-acetyl-L-tryptophan ] 1.23 -0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[N-acetyl-D-tyrosine] 2.09 0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[N-acetyl-D-tyrosine] 2.10 0.30 6.9 25.0 Isothermal titration calorimetry Yoshihisa Inoue 2004
[b-Cyclodextrin](1).[(R)-camphanic acid ] 2.25 0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(S)-camphanic acid ] 2.32 0.48 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(R)-10-camphorsulfonic acid] 2.75 1.00 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(S)-10-camphorsulfonic acid ] 2.69 1.00 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[3-(2-hydroxyphenyl)- propionicacid ] 1.91 0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[3-(4-hydroxyphenyl)-propionicacid ] 2.47 0.60 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(R)-a-methoxy-a-trifluoromethylphenylacetic acid ] 2.24 0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(S)-a-methoxy-a-trifluoromethylphenylacetic acid ] 2.15 0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[cyclohexenonecarboxylate] 2.42 7.0 25.0 UV-vis spectroscopy, circular dichroism spectroscopy Kiyomi Kakuchi 2006
[b-Cyclodextrin](1).[sodium hexaflouro-phosphate ] 2.01 0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[sodium perchlorate] 1.18 -0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[sodium thiocyanate ] 0.70 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[3-tolylacetic acid] 1.08 0.15 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[4-tolylacetic acid ] 1.61 0.23 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[N-acetyl-D-phenylalanine] 1.78 0.11 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[N-t-Boc-D-alanine ] 2.59 0.60 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[N-t-Boc-L-alanine] 2.56 0.60 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[N-Cbz-D-alanine ] 2.17 0.60 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[N-Cbz-D-alanine ] 2.18 0.78 7.2 25.0 Microcalorimetric titrations Yu Liu 2003
[b-Cyclodextrin](1).[N-Cbz-D-alanine ] 2.17 0.60 Microcalorimetric titrations Yu Liu 2003
[b-Cyclodextrin](1).[N-Cbz-D-aspartic acid ] 1.85 0.18 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[N-Cbz-L-aspartic acid ] 1.87 0.18 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(R)-2-phenylbutyric acid] 1.97 0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(S)-2-phenylbutyric acid ] 1.98 0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(R)-3-phenylbutyric acid ] 2.60 0.60 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(S)-3-phenylbutyric acid ] 2.63 0.60 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(R)-phenyllactic acid ] 1.94 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(S)-phenyllactic acid ] 1.92 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[3-phenylpropionic acid] 2.21 0.60 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[4-tolylic acid (-1)] 1.98 0.48 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[O,O'-dibenzoyl-D-tartaric acid] 1.51 0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[O,O'-dibenzoyl-L-tartaric acid] 1.30 0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[O,O'-di-p-toluoyl-D-tartaric acid] 2.02 0.78 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[O,O'-di-p-toluoyl-L-tartaric acid] 1.97 0.90 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[Gly-D-Phe (zwitterion) ] 1.67 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[Gly-L-Phe (zwitterion) ] 1.73 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(S)-hexahydromandelic acid] 2.78 1.00 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(R)-mandelic acid ] 1.04 0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(S)-mandelic acid] 0.95 0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(R)-a-methoxyphenylacetic acid] 1.04 0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(S)-a-methoxyphenylacetic acid] 1.00 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[N-t-Boc-D-alanine methyl ester] 2.82 0.78 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(R)-3-bromo-2-methyl-1-propanol ] 2.15 0.60 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(S)-3-bromo-2-methyl-1-propanol ] 2.15 0.60 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(R)-1-cyclohexylethyl-amine ] 2.52 0.48 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[skatol] 2.18 1.48 7.0 25.0 UV-vis spectroscopy, fluorescence spectroscopy Alicia V. Veglia 2005
[b-Cyclodextrin](1).[(S)-1-cyclohexylethyl-amine ] 2.52 0.48 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(R)-mandelic acid methyl ester] 1.83 0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[(S)-mandelic acid methyl ester] 1.86 0.30 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[1-methyl-3-phenylpropyl-amine ] 2.27 0.48 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[b-Cyclodextrin](1).[auxin] 1.78 1.48 7.0 25.0 UV-vis spectroscopy, fluorescence spectroscopy Alicia V. Veglia 2005
[b-Cyclodextrin](1).[auxin] 2.04 1.48 3.0 25.0 UV-vis spectroscopy, fluorescence spectroscopy Alicia V. Veglia 2005
[b-Cyclodextrin](1).[N-Methyl-N-nitroso-p-toluenesulphonamide] 3.19 1.30 1.0 25.0 UV-vis spectroscopy L. Garcia-Rio 2005
[b-Cyclodextrin](2).[neutral red] 2.62 2.00 9.0 25.0 Fluorescence spectroscopy M. K. Singh 2004
[b-Cyclodextrin](1).[2-chloroethylnitrososulfamides derivative 1] 3.78 2.00 20.0 UV-vis spectroscopy Mohamed Abdaoui 2004
[b-Cyclodextrin](1).[2-chloroethylnitrososulfamides derivative 2] 4.40 2.18 20.0 UV-vis spectroscopy Mohamed Abdaoui 2004
[b-Cyclodextrin](1).[2-chloroethylnitrososulfamides derivative 3] 3.99 2.00 20.0 UV-vis spectroscopy Mohamed Abdaoui 2004
[b-Cyclodextrin](1).[2-chloroethylnitrososulfamides derivative 4] 4.39 2.18 20.0 UV-vis spectroscopy Mohamed Abdaoui 2004
[b-Cyclodextrin](1).[N,N-diethyl-2-(1-naphthalenyloxy)propanamide] 3.50 2.2 25.0 Fluorescence spectroscopy Bo Tang 2004
[b-Cyclodextrin](2).[5,11,17,23-Tetraguanidinium-25,27-bis(2-ethoxyethoxy)-26,28-bis(2-(2-(2-(2-(adamantyl-1-oxy)ethoxy)ethoxy)ethoxy)ethoxy)calix[4]-arene tetraacetate] 4.66 3.48 Calorimetric titrations Jurriaan Huskens 2004
[b-Cyclodextrin](1).[methanol] 0.11 -1.00 1.0 25.0 UV-vis spectroscopy L. Garcia-Rio 2005
[b-Cyclodextrin](1).[2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid 3-tetrahydrofurfuryl 5-methyl diester] 2.19 7.0 37.0 UV-vis spectroscopy J.A. Squella 2004
[b-Cyclodextrin](1).[2-amino-7-bromofluorene] 2.75 10.0 Fluorescence spectroscopy M. Swaminathan 2004
[b-Cyclodextrin](1).[Pb(II) nitrate] 2.86 1.31 Cyclic voltammetry Maria Teresa Ramirez-Silva 2005
[b-Cyclodextrin](1).[dequalinium chloride] 2.81 1.3 10.0 Fluorescence spectroscopy Bo Tang 2005
[b-Cyclodextrin](1).[dequalinium chloride] 2.70 1.3 20.0 Fluorescence spectroscopy Bo Tang 2005
[b-Cyclodextrin](1).[dequalinium chloride] 2.60 1.3 30.0 Fluorescence spectroscopy Bo Tang 2005
[b-Cyclodextrin](1).[dequalinium chloride] 2.48 1.3 40.0 Fluorescence spectroscopy Bo Tang 2005
[b-Cyclodextrin](1).[dequalinium chloride] 2.37 1.3 50.0 Fluorescence spectroscopy Bo Tang 2005
[b-Cyclodextrin](1).[dodecyltrimethylammonium chloride] 4.23 2.85 7.0 25.0 Fluorescence spectroscopy Catherine Amiel 2005
[b-Cyclodextrin](1).[dodecyltrimethylammonium chloride] 4.18 23.0 Surface plasmon resonance Véronique Wintgens 2005
[b-Cyclodextrin](1).[4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl] 2.76 1.95 7.0 15.0 Fluorescence spectroscopy Jamshid L. Manzoori 2005
[b-Cyclodextrin](1).[4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl] 2.69 1.78 7.0 25.0 Fluorescence spectroscopy Jamshid L. Manzoori 2005
[b-Cyclodextrin](1).[4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl] 2.65 1.60 7.0 30.0 Fluorescence spectroscopy Jamshid L. Manzoori 2005
[b-Cyclodextrin](1).[4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl] 2.61 1.78 7.0 35.0 Fluorescence spectroscopy Jamshid L. Manzoori 2005
[b-Cyclodextrin](1).[4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl] 2.56 1.60 7.0 40.0 Fluorescence spectroscopy Jamshid L. Manzoori 2005
[b-Cyclodextrin](1).[4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl] 2.53 1.78 7.0 45.0 Fluorescence spectroscopy Jamshid L. Manzoori 2005
[b-Cyclodextrin](1).[naproxen] 3.23 5.0 25.0 UV-vis spectroscopy P. Mura 2005
[b-Cyclodextrin](1).[naproxen] 3.14 5.0 37.0 UV-vis spectroscopy P. Mura 2005
[b-Cyclodextrin](1).[naproxen] 2.62 9.0 25.0 NMR spectroscopy A. Ganza-Gonzalez 1994
[b-Cyclodextrin](1).[naproxen] 1.59 7.4 37.0 UV-vis spectroscopy Francesco Castelli 1992
[b-Cyclodextrin](1).[naproxen] 2.99 1.52 7.0 25.0 UV-vis spectroscopy Margarita Valero 2003
[b-Cyclodextrin](1).[naproxen] 2.80 1.70 10.5 25.0 Gradient flow injection spectrophotometric technique Michael A. Koupparis 1995
[b-Cyclodextrin](1).[ethanol] 0.65 -0.05 1.0 25.0 UV-vis spectroscopy L. Garcia-Rio 2005
[b-Cyclodextrin](1).[eugenol] 5.60 7.0 20.0 UV-vis spectroscopy Le Xin Song 2005
[b-Cyclodextrin](1).[methyldimethylbenzylammonium bromide] 1.09 -1.00 25.0 UV-vis spectroscopy B. Tutaj 2005
[b-Cyclodextrin](1).[1-propanol] 0.97 -0.30 1.0 25.0 UV-vis spectroscopy L. Garcia-Rio 2005
[b-Cyclodextrin](1).[1-propanol] 0.65 0.23 6.9 25.0 Titration calorimetry Robert N. Goldberg 1994
[b-Cyclodextrin](1).[ethyldimethylbenzylammonium bromide] 1.04 25.0 UV-vis spectroscopy B. Tutaj 2005
[b-Cyclodextrin](1).[propyldimethylbenzylammonium bromide] 1.59 25.0 UV-vis spectroscopy B. Tutaj 2005
[b-Cyclodextrin](1).[butyldimethylbenzylammonium bromide] 2.41 0.78 25.0 UV-vis spectroscopy B. Tutaj 2005
[b-Cyclodextrin](1).[hexyldimethylbenzylammonium bromide] 2.85 1.67 25.0 UV-vis spectroscopy B. Tutaj 2005
[b-Cyclodextrin](1).[decyldimethylbenzylammonium bromide] 3.83 2.39 25.0 UV-vis spectroscopy B. Tutaj 2005
[b-Cyclodextrin](1).[dodecyldimethylbenzylammonium bromide] 4.29 2.68 25.0 UV-vis spectroscopy B. Tutaj 2005
[b-Cyclodextrin](1).[phenolphtalein] 4.39 2.30 25.0 UV-vis spectroscopy B. Tutaj 2005
[b-Cyclodextrin](1).[phenolphtalein] 4.39 2.00 11.0 25.0 UV and NMR spectroscopy Yoshihisa Matsui 1994
[b-Cyclodextrin](1).[phenolphtalein] 4.37 2.00 11.4 25.0 UV and NMR spectroscopy Yoshihisa Matsui 1994
[b-Cyclodextrin](1).[phenolphtalein] 4.37 2.00 11.6 25.0 UV and NMR spectroscopy Yoshihisa Matsui 1994
[b-Cyclodextrin](1).[phenolphtalein] 4.87 10.5 10.0 UV-vis spectroscopy Henryk Lamparczyk 1998
[b-Cyclodextrin](1).[phenolphtalein] 4.60 10.5 20.0 UV-vis spectroscopy Henryk Lamparczyk 1998
[b-Cyclodextrin](1).[phenolphtalein] 4.34 10.5 30.0 UV-vis spectroscopy Henryk Lamparczyk 1998
[b-Cyclodextrin](1).[phenolphtalein] 4.08 10.5 40.0 UV-vis spectroscopy Henryk Lamparczyk 1998
[b-Cyclodextrin](1).[phenolphtalein] 3.88 10.5 50.0 UV-vis spectroscopy Henryk Lamparczyk 1998
[b-Cyclodextrin](1).[phenolphtalein] 3.64 10.5 60.0 UV-vis spectroscopy Henryk Lamparczyk 1998
[b-Cyclodextrin](1).[phenolphtalein] 2.41 10.5 70.0 UV-vis spectroscopy Henryk Lamparczyk 1998
[b-Cyclodextrin](1).[2-allylphenol] 2.31 7.0 22.0 UV-vis spectroscopy Sandra Monti 2005
[b-Cyclodextrin](1).[2-allylphenol] 2.39 7.0 22.0 Fluorescence spectroscopy Sandra Monti 2005
[b-Cyclodextrin](1).[2-allylphenol] 2.46 7.0 22.0 Circular dichroism spectroscopy Sandra Monti 2005
[b-Cyclodextrin](1).[2-allylanisole] 2.36 7.0 22.0 UV-vis spectroscopy Sandra Monti 2005
[b-Cyclodextrin](1).[2-allylanisole] 2.80 7.0 22.0 Fluorescence spectroscopy Sandra Monti 2005
[b-Cyclodextrin](1).[2-allylanisole] 2.36 7.0 22.0 Circular dichroism spectroscopy Sandra Monti 2005
[b-Cyclodextrin](1).[2-allylaniline] 2.18 7.0 22.0 Fluorescence spectroscopy Sandra Monti 2005
[b-Cyclodextrin](1).[2-propanol] 0.94 -0.10 1.0 25.0 UV-vis spectroscopy L. Garcia-Rio 2005
[b-Cyclodextrin](1).[2-propanol] 0.41 -0.30 6.9 25.0 Titration calorimetry Robert N. Goldberg 1994
[b-Cyclodextrin](1).[bis (dodecyldimethylammonium)diethyl ether dibromide] 3.90 3.70 7.0 25.0 NMR spectroscopy Gloria Tardajos 2006
[b-Cyclodextrin](2).[bis (dodecyldimethylammonium)diethyl ether dibromide] 4.45 3.95 7.0 25.0 NMR spectroscopy Gloria Tardajos 2006
[b-Cyclodextrin](1).[naringin] 3.01 2.18 20.0 UV-vis spectroscopy Soundar Divakar 1993
[b-Cyclodextrin](1).[nimesulide] 2.73 7.0 25.0 UV-vis spectroscopy M.I. La Rotonda 2000
[b-Cyclodextrin](1).[nimesulide] 2.72 7.7 25.0 HPLC-method Eric Peyrin 2002
[b-Cyclodextrin](1).[nimesulide] 2.66 7.7 30.0 HPLC-method Eric Peyrin 2002
[b-Cyclodextrin](1).[nimesulide] 2.59 7.7 35.0 HPLC-method Eric Peyrin 2002
[b-Cyclodextrin](1).[nimesulide] 2.55 7.7 40.0 HPLC-method Eric Peyrin 2002
[b-Cyclodextrin](1).[2-cyano-3-(1,4-dihydro-1-phenyl-(1)-benzothiopyran-(4,3-C)-pyrazol-3-yl)-3-oxo-N-phenyl-propanamide] 2.84 7.4 37.0 UV-vis spectroscopy Roberto DePonti 1991
[b-Cyclodextrin](1).[2-cyano-3-(1,4-dihydro-1-phenyl-(1)-benzothiopyran-(4,3-C)-pyrazol-3-yl)-3-oxo-N-phenyl-propanamide] 3.02 7.4 37.0 Polarography Roberto DePonti 1991
[b-Cyclodextrin](1).[4-[4-(dimethylamino)phenylazo]benzoic acid] -2.39 -3.60 1.0 16.0 UV-vis spectroscopy Khalid M. Tawarah 1993
[b-Cyclodextrin](1).[4-[4-(dimethylamino)phenylazo]benzoic acid] -2.50 -3.68 1.0 25.0 UV-vis spectroscopy Khalid M. Tawarah 1993
[b-Cyclodextrin](1).[4-[4-(dimethylamino)phenylazo]benzoic acid] -2.58 -4.30 1.0 33.0 UV-vis spectroscopy Khalid M. Tawarah 1993
[b-Cyclodextrin](1).[4-[4-(dimethylamino)phenylazo]benzoic acid] -2.66 -4.00 1.0 40.5 UV-vis spectroscopy Khalid M. Tawarah 1993
[b-Cyclodextrin](1).[4-[4-(dimethylamino)phenylazo]benzoic acid] -2.29 -4.00 9.5 16.0 UV-vis spectroscopy Khalid M. Tawarah 1993
[b-Cyclodextrin](1).[4-[4-(dimethylamino)phenylazo]benzoic acid] -2.42 -3.96 9.5 25.0 UV-vis spectroscopy Khalid M. Tawarah 1993
[b-Cyclodextrin](1).[4-[4-(dimethylamino)phenylazo]benzoic acid] -2.49 -4.22 9.5 33.0 UV-vis spectroscopy Khalid M. Tawarah 1993
[b-Cyclodextrin](1).[4-[4-(dimethylamino)phenylazo]benzoic acid] -2.57 -4.52 9.5 40.5 UV-vis spectroscopy Khalid M. Tawarah 1993
[b-Cyclodextrin](1).[Rocuronium Bromide] 3.52 2.70 30.0 NMR spectroscopy Lee Fielding 2002
[b-Cyclodextrin](1).[progesterone] 4.39 7.0 30.0 UV-vis spectroscopy Ashim K. Mitra 1990
[b-Cyclodextrin](2).[progesterone] 2.84 7.0 30.0 UV-vis spectroscopy Ashim K. Mitra 1990
[b-Cyclodextrin](1).[2-butanol] 1.30 -0.05 1.0 25.0 UV-vis spectroscopy L. Garcia-Rio 2005
[b-Cyclodextrin](1).[testosterone] 3.70 7.0 30.0 UV-vis spectroscopy Ashim K. Mitra 1990
[b-Cyclodextrin](2).[testosterone] 3.44 7.0 30.0 UV-vis spectroscopy Ashim K. Mitra 1990
[b-Cyclodextrin](1).[hydrocortisone] 3.43 7.0 30.0 UV-vis spectroscopy Ashim K. Mitra 1990
[b-Cyclodextrin](2).[hydrocortisone] 2.15 7.0 30.0 UV-vis spectroscopy Ashim K. Mitra 1990
[b-Cyclodextrin](1).[cortisone] 3.42 7.0 30.0 UV-vis spectroscopy Ashim K. Mitra 1990
[b-Cyclodextrin](2).[cortisone] 3.76 7.0 30.0 UV-vis spectroscopy Ashim K. Mitra 1990
[b-Cyclodextrin](1).[4-hydroxyphenylmethanol] 2.16 0.48 7.0 25.0 Fluorescence spectroscopy Koji Kano 1992
[b-Cyclodextrin](1).[2-(4-hydroxyphenyl)ethanol] 2.52 1.28 7.0 25.0 Fluorescence spectroscopy Koji Kano 1992
[b-Cyclodextrin](1).[3-(4-hydroxyphenyl)propanol] 2.98 1.56 7.0 25.0 Fluorescence spectroscopy Koji Kano 1992
[b-Cyclodextrin](1).[3-(4-hydroxyphenyl)propanol] 3.07 7.0 15.0 Fluorescence spectroscopy Koji Kano 1992
[b-Cyclodextrin](1).[3-(4-hydroxyphenyl)propanol] 3.02 7.0 20.0 Fluorescence spectroscopy Koji Kano 1992
[b-Cyclodextrin](1).[3-(4-hydroxyphenyl)propanol] 2.98 7.0 30.0 Fluorescence spectroscopy Koji Kano 1992
[b-Cyclodextrin](1).[3-(4-hydroxyphenyl)propanol] 2.95 7.0 35.0 Fluorescence spectroscopy Koji Kano 1992
[b-Cyclodextrin](1).[4-ethylphenol] 2.69 1.26 7.0 25.0 Fluorescence spectroscopy Koji Kano 1992
[b-Cyclodextrin](1).[4-ethylphenol] 2.72 5.8 20.0 UV-vis spectroscopy; spectral displacement method D. Landy 2000
[b-Cyclodextrin](1).[4-propylphenol] 3.42 2.29 7.0 25.0 Fluorescence spectroscopy Koji Kano 1992
[b-Cyclodextrin](1).[4-butylphenol] 3.61 2.30 7.0 25.0 Fluorescence spectroscopy Koji Kano 1992
[b-Cyclodextrin](1).[retinol] 3.56 25.0 UV-vis spectroscopy Qing-Xiang Guo 1995
[b-Cyclodextrin](1).[isobutanol] 1.55 0.58 1.0 25.0 UV-vis spectroscopy L. Garcia-Rio 2005
[b-Cyclodextrin](1).[retinal] 3.56 25.0 UV-vis spectroscopy Qing-Xiang Guo 1995
[b-Cyclodextrin](1).[retinoic acid] 3.53 25.0 UV-vis spectroscopy Qing-Xiang Guo 1995
[b-Cyclodextrin](1).[NADH] 0.65 6.0 25.0 HPLC-method Manabu Seno 1990
[b-Cyclodextrin](1).[NADP] 0.85 6.0 25.0 HPLC-method Manabu Seno 1990
[b-Cyclodextrin](2).[tolbutamide] 3.32 7.0 25.0 UV-vis spectroscopy F. Kedzierewicz 1990
[b-Cyclodextrin](1).[celecoxib] 2.77 7.0 37.0 UV-vis spectroscopy V. R. Sinha 2005
[b-Cyclodextrin](1).[celecoxib] 2.95 6.8 25.0 UV-vis spectroscopy Swati Rawat 2004
[b-Cyclodextrin](1).[(S)-(+)-6-methoxy-a-methyl-2-naphthaleneacetic acid] 3.32 0.02 2.5 20.0 Fluorescence spectroscopy Graciela M. Escandar 2001
[b-Cyclodextrin](1).[(S)-(+)-6-methoxy-a-methyl-2-naphthaleneacetic acid] 3.00 0.30 2.5 20.0 Potentiometry Graciela M. Escandar 2001
[b-Cyclodextrin](1).[(S)-(+)-6-methoxy-a-methyl-2-naphthaleneacetic acid] 2.71 0.02 10.0 20.0 Fluorescence spectroscopy Graciela M. Escandar 2001
[b-Cyclodextrin](1).[(S)-(+)-6-methoxy-a-methyl-2-naphthaleneacetic acid] 2.80 0.30 10.0 20.0 Potentiometry Graciela M. Escandar 2001
[b-Cyclodextrin](1).[4-biphenylacetic acid] 2.43 7.4 37.0 UV-vis spectroscopy Francesco Castelli 1992
[b-Cyclodextrin](1).[ketoprofen] 1.28 7.4 37.0 UV-vis spectroscopy Francesco Castelli 1992
[b-Cyclodextrin](1).[ketoprofen] 2.59 8.0 25.0 HPLC-method E. Antoniadou-Vyza 2005
[b-Cyclodextrin](1).[4-Methoxyindole] 2.21 0.48 7.0 18.0 HPLC-method Arantza Zornoza 2005
[b-Cyclodextrin](1).[anetholetrithione] 3.45 7.0 37.0 HPLC-method Gilles Dollo 1999
[b-Cyclodextrin](1).[5-phenyldithiolethione] 3.37 7.0 37.0 HPLC-method Gilles Dollo 1999
[b-Cyclodextrin](1).[dimethyldithiolethione] 2.61 7.0 37.0 HPLC-method Gilles Dollo 1999
[b-Cyclodextrin](1).[dithiolethione] 2.08 7.0 37.0 HPLC-method Gilles Dollo 1999
[b-Cyclodextrin](1).[Nitrazepam ] 1.98 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[b-Cyclodextrin](1).[Nimetazepam ] 1.74 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[b-Cyclodextrin](1).[Flunitrazepam ] 1.89 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[b-Cyclodextrin](1).[Pindolol] 1.71 0.30 7.0 18.0 HPLC-method Arantza Zornoza 2005
[b-Cyclodextrin](1).[Pindolol] 1.87 0.70 12.0 25.0 HPLC-method Arantza Zornoza 2005
[b-Cyclodextrin](1).[Clonazepam ] 1.90 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[b-Cyclodextrin](1).[Flurazepam ] 2.08 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[b-Cyclodextrin](1).[Lorazepam ] 2.51 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[b-Cyclodextrin](1).[oxazepam ] 2.23 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[b-Cyclodextrin](1).[Clobazam ] 1.69 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[b-Cyclodextrin](2).[Chlordiazepoxide] 2.65 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[b-Cyclodextrin](1).[2-(2-fluoro-4-biphenylyl)propionic acid] 3.77 7.0 15.0 UV-vis spectroscopy Kaneto Uekama 1985
[b-Cyclodextrin](1).[2-(2-fluoro-4-biphenylyl)propionic acid] 3.64 7.0 25.0 UV-vis spectroscopy Kaneto Uekama 1985
[b-Cyclodextrin](1).[2-(2-fluoro-4-biphenylyl)propionic acid] 3.56 7.0 37.0 UV-vis spectroscopy Kaneto Uekama 1985
[b-Cyclodextrin](1).[2-(2-fluoro-4-biphenylyl)propionic acid] 3.52 7.0 45.0 UV-vis spectroscopy Kaneto Uekama 1985
[b-Cyclodextrin](1).[( 5Z, 13E)-(9R, 11 R, 15R)-9-chloro-11,15-dihydroxy-16,16-dimethyl-5,13-prostadienoic acid] 3.46 7.0 15.0 UV-vis spectroscopy Kaneto Uekama 1990
[b-Cyclodextrin](1).[( 5Z, 13E)-(9R, 11 R, 15R)-9-chloro-11,15-dihydroxy-16,16-dimethyl-5,13-prostadienoic acid] 3.37 7.0 25.0 UV-vis spectroscopy Kaneto Uekama 1990
[b-Cyclodextrin](1).[( 5Z, 13E)-(9R, 11 R, 15R)-9-chloro-11,15-dihydroxy-16,16-dimethyl-5,13-prostadienoic acid] 3.30 7.0 35.0 UV-vis spectroscopy Kaneto Uekama 1990
[b-Cyclodextrin](1).[2-dibenzofuran carboxylate] 3.26 1.95 10.0 27.0 NMR spectroscopy Gustavo González-Gaitano 2004
[b-Cyclodextrin](1).[hydrocortisone butyrate ] 3.43 4.0 20.0 Solubility method (UV-vis spectroscopy) In Koo Chun 1993
[b-Cyclodextrin](1).[hydrocortisone butyrate ] 3.25 4.0 30.0 Solubility method (UV-vis spectroscopy) In Koo Chun 1993
[b-Cyclodextrin](1).[hydrocortisone butyrate ] 3.16 4.0 37.0 Solubility method (UV-vis spectroscopy) In Koo Chun 1993
[b-Cyclodextrin](1).[hydrocortisone butyrate ] 3.23 4.0 25.0 Circular dichroism spectroscopy In Koo Chun 1993
[b-Cyclodextrin](1).[hydrocortisone butyrate ] 3.16 4.0 25.0 UV-vis spectroscopy In Koo Chun 1993
[b-Cyclodextrin](1).[sodium pentyl sulfate] 2.00 1.00 7.0 25.0 NMR spectroscopy Qing-Xiang Guo 1994
[b-Cyclodextrin](1).[sodium hexyl sulfate] 2.16 1.57 7.0 25.0 NMR spectroscopy Qing-Xiang Guo 1994
[b-Cyclodextrin](1).[sodium heptyl sulfate] 2.49 1.85 7.0 25.0 NMR spectroscopy Qing-Xiang Guo 1994
[b-Cyclodextrin](1).[sodium octyl sulfate] 2.54 1.04 7.0 25.0 NMR spectroscopy Qing-Xiang Guo 1994
[b-Cyclodextrin](1).[sodium nonyl sulfate] 3.08 2.46 7.0 25.0 NMR spectroscopy Qing-Xiang Guo 1994
[b-Cyclodextrin](1).[sodium decyl sulfate] 3.35 2.18 7.0 25.0 NMR spectroscopy Qing-Xiang Guo 1994
[b-Cyclodextrin](1).[sodium octanoate] 2.66 1.85 7.0 20.0 NMR spectroscopy Gustavo González-Gaitano 2004
[b-Cyclodextrin](1).[sodium octanoate] 2.82 1.78 7.0 25.0 NMR spectroscopy G. Tardajos 1999
[b-Cyclodextrin](1).[warfarin] 2.73 1.28 7.4 37.0 Fluorescence spectroscopy Serdar Ates 1994
[b-Cyclodextrin](1).[warfarin] 2.72 7.4 37.0 High-performance affinity chromatography David S. Hage 2004
[b-Cyclodextrin](1).[warfarin] 2.80 1.2 37.0 UV spectroscopy G. Zingone 2005
[b-Cyclodextrin](1).[warfarin] 2.49 5.0 37.0 UV spectroscopy G. Zingone 2005
[b-Cyclodextrin](1).[warfarin] 2.00 7.4 37.0 UV spectroscopy G. Zingone 2005
[b-Cyclodextrin](1).[warfarin] 2.47 5.5 37.0 UV spectroscopy G. Zingone 2005
[b-Cyclodextrin](1).[warfarin] 2.74 9.5 25.0 fluorescence spectroscopy Mamoru Kamiya 1997
[b-Cyclodextrin](1).[warfarin] 2.73 7.4 fluorescence spectroscopy Mamoru Kamiya 1997
[b-Cyclodextrin](1).[warfarin] 2.72 HPLC Mamoru Kamiya 1997
[b-Cyclodextrin](1).[warfarin] 2.17 infrared spectroscopy, differencial scanning calorimetry Mamoru Kamiya 1997
[b-Cyclodextrin](1).[2-amino-5-bromo-6-phenyl-pyrimidin-4(3H)-one] 2.41 7.0 25.0 UV-vis spectroscopy S.M. Ahmed 1991
[b-Cyclodextrin](1).[2-amino-5-bromo-6-phenyl-pyrimidin-4(3H)-one] 2.35 7.0 30.0 UV-vis spectroscopy S.M. Ahmed 1991
[b-Cyclodextrin](1).[2-amino-5-bromo-6-phenyl-pyrimidin-4(3H)-one] 2.33 7.0 37.0 UV-vis spectroscopy S.M. Ahmed 1991
[b-Cyclodextrin](1).[2-amino-5-bromo-6-phenyl-pyrimidin-4(3H)-one] 2.29 7.0 45.0 UV-vis spectroscopy S.M. Ahmed 1991
[b-Cyclodextrin](1).[L-Phe ] 1.23 -0.22 7.4 23.0 UV-vis spectroscopy Jiri Horsky 1994
[b-Cyclodextrin](1).[Gly-D-Phe ] 1.83 0.08 7.4 23.0 UV-vis spectroscopy Jiri Horsky 1994
[b-Cyclodextrin](1).[L-PheGly ] 1.76 0.54 7.4 23.0 UV-vis spectroscopy Jiri Horsky 1994
[b-Cyclodextrin](1).[GlyGly-L-Phe ] 1.95 0.28 7.4 23.0 UV-vis spectroscopy Jiri Horsky 1994
[b-Cyclodextrin](1).[Gly-L-Tyr ] 2.00 0.30 7.4 23.0 UV-vis spectroscopy Jiri Horsky 1994
[b-Cyclodextrin](1).[sodium decanoate] 3.04 2.78 7.0 20.0 NMR spectroscopy Gustavo González-Gaitano 2004
[b-Cyclodextrin](1).[sodium decanoate] 3.36 2.78 7.0 25.0 NMR spectroscopy G. Tardajos 1999
[b-Cyclodextrin](1).[L-TrpGly ] 1.72 0.18 7.4 23.0 UV-vis spectroscopy Jiri Horsky 1994
[b-Cyclodextrin](1).[Adenine ] 1.15 7.0 25.0 UV-vis spectroscopy Bradley D. Anderson 1990
[b-Cyclodextrin](1).[6-(DimethyIamino)-adenine] 1.50 0.77 7.0 25.0 UV-vis spectroscopy Bradley D. Anderson 1990
[b-Cyclodextrin](1).[Adenosine] 1.12 7.0 25.0 UV-vis spectroscopy Bradley D. Anderson 1990
[b-Cyclodextrin](1).[2’-Deoxyadenosine] 1.40 0.76 7.0 25.0 UV-vis spectroscopy Bradley D. Anderson 1990
[b-Cyclodextrin](1).[3’-Deoxyadenosine ] 1.40 0.81 7.0 25.0 Circular dichroism spectroscopy Bradley D. Anderson 1990
[b-Cyclodextrin](1).[5’-Deoxyadenosine ] 1.34 0.18 7.0 25.0 Circular dichroism spectroscopy Bradley D. Anderson 1990
[b-Cyclodextrin](1).[2’,3’-Dideoxyadenosine ] 1.47 1.03 7.0 25.0 Circular dichroism spectroscopy Bradley D. Anderson 1990
[b-Cyclodextrin](1).[N-(1,1-dimethylethyl)-4-hydroxybenzene-1,2-dicarboximide] 3.47 2.5 25.0 Fluorescence spectroscopy Noelle Martine Gosselet 2005
[b-Cyclodextrin](1).[adenine arabinoside] 1.63 0.73 7.0 25.0 UV-vis spectroscopy Bradley D. Anderson 1990
[b-Cyclodextrin](1).[6-(Dimethylamino)-adenosine ] 2.11 1.02 7.0 25.0 Circular dichroism spectroscopy Bradley D. Anderson 1990
[b-Cyclodextrin](1).[3-[2-[4-(3-chloro-2-methylphenyl)-1-piperazinyl]ethyl]-5,6-dimethoxy-1-(4-imidazolylmethyl)-1H-indazole dihydrochloride 3.5 hydrate] 2.92 2.50 4.0 15.0 Circular dichroism spectroscopy Kaneto Uekama 2003
[b-Cyclodextrin](1).[3-[2-[4-(3-chloro-2-methylphenyl)-1-piperazinyl]ethyl]-5,6-dimethoxy-1-(4-imidazolylmethyl)-1H-indazole dihydrochloride 3.5 hydrate] 2.79 2.23 4.0 25.0 Circular dichroism spectroscopy Kaneto Uekama 2003
[b-Cyclodextrin](1).[3-[2-[4-(3-chloro-2-methylphenyl)-1-piperazinyl]ethyl]-5,6-dimethoxy-1-(4-imidazolylmethyl)-1H-indazole dihydrochloride 3.5 hydrate] 2.74 2.34 4.0 30.0 Circular dichroism spectroscopy Kaneto Uekama 2003
[b-Cyclodextrin](1).[3-[2-[4-(3-chloro-2-methylphenyl)-1-piperazinyl]ethyl]-5,6-dimethoxy-1-(4-imidazolylmethyl)-1H-indazole dihydrochloride 3.5 hydrate] 2.63 1.76 4.0 37.0 Circular dichroism spectroscopy Kaneto Uekama 2003
[b-Cyclodextrin](1).[3-[2-[4-(3-chloro-2-methylphenyl)-1-piperazinyl]ethyl]-5,6-dimethoxy-1-(4-imidazolylmethyl)-1H-indazole dihydrochloride 3.5 hydrate] 2.63 1.70 4.0 37.0 Circular dichroism K. Uekama 2001
[b-Cyclodextrin](1).[N-(1,1-dimethylethyl)-4-aminobenzene-1,2-dicarboximide] 3.51 7.0 25.0 Fluorescence spectroscopy Noelle Martine Gosselet 2005
[b-Cyclodextrin](1).[Diphenidol HCl] 2.97 1.94 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[b-Cyclodextrin](1).[Diphenhydramine HCI] 3.06 1.59 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[b-Cyclodextrin](1).[DM17] 2.48 2.5 25.0 Fluorescence spectroscopy Noelle Martine Gosselet 2005
[b-Cyclodextrin](1).[DM17] 1.95 7.0 25.0 Fluorescence spectroscopy Noelle Martine Gosselet 2005
[b-Cyclodextrin](1).[Orphenadrine HCI ] 3.11 1.93 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[b-Cyclodextrin](1).[Bromodiphenhydramine HCl ] 3.33 2.43 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[b-Cyclodextrin](1).[Diphenylpyraline HCI ] 3.36 2.12 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[b-Cyclodextrin](1).[Cyclizine HCl] 3.08 1.98 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[b-Cyclodextrin](1).[Chlorcyclizine HCI] 3.39 2.53 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[b-Cyclodextrin](1).[Chlorcyclizine 2HCl] 3.38 1.98 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[b-Cyclodextrin](1).[Meclizine 2HCl] 3.35 2.40 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[b-Cyclodextrin](1).[Hydroxyzine HCI] 3.36 2.01 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[b-Cyclodextrin](1).[Proadifen HCl] 2.96 1.71 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[b-Cyclodextrin](1).[MS-325] 4.90 7.0 25.0 Proton Relaxation Enhancement Method Silvio Aime 2006
[b-Cyclodextrin](1).[Adiphenine HCl ] 3.44 2.24 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[b-Cyclodextrin](1).[itraconazole] 2.95 7.4 25.0 UV-vis spectroscopy Ali H. Al-Marzouqi 2006
[b-Cyclodextrin](1).[Azure A] 2.04 1.60 10.5 20.0 Fluorescence spectroscopy Jean-Jacques Aaron 1995
[b-Cyclodextrin](1).[triflumizole] 2.67 25.0 UV-vis spectroscopy Th. Ch. Klein 1995
[b-Cyclodextrin](1).[triflumizole] 2.67 1.30 7.0 25.0 UV-vis spectroscopy H. Viernstein 1994
[b-Cyclodextrin](1).[methyl orange] 3.55 7.2 25.0 Circular dichroism spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[methyl orange] 2.55 0.60 0.7 25.0 UV and NMR spectroscopy Yoshihisa Matsui 1994
[b-Cyclodextrin](1).[methyl orange] 3.55 7.2 25.0 circular dichroism spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[methyl orange] 3.55 7.2 25.0 circular dichroism Yu Liu 2002
[b-Cyclodextrin](1).[methyl orange] 1.84 25.0 spectrophotometry Hans-Jürgen Buschmann 1997
[b-Cyclodextrin](1).[methyl orange] 2.43 1.1 25.0 spectrophotometry Hans-Jürgen Buschmann 1997
[b-Cyclodextrin](1).[amitriptylin] 4.38 1.70 6.0 25.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[amitriptylin] 4.79 2.48 6.0 5.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[amitriptylin] 4.58 2.00 6.0 15.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[amitriptylin] 4.17 1.78 6.0 37.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[notriptylin] 4.22 1.78 6.0 25.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[notriptylin] 4.57 2.48 6.0 5.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[notriptylin] 4.38 2.30 6.0 15.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[notriptylin] 3.92 1.70 6.0 37.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[doxepin] 4.12 1.85 6.0 25.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[doxepin] 4.62 2.48 6.0 5.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[doxepin] 4.35 2.00 6.0 15.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[doxepin] 3.88 1.48 6.0 37.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[imipramin] 3.94 1.78 6.0 25.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[imipramin] 4.29 2.00 6.0 5.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[imipramin] 4.18 2.30 6.0 15.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[imipramin] 3.73 1.48 6.0 37.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[protriptylin] 4.26 1.85 6.0 25.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[protriptylin] 4.61 2.60 6.0 5.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[protriptylin] 4.43 2.30 6.0 15.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[protriptylin] 4.04 2.00 6.0 37.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[maprotilin] 3.68 1.30 6.0 25.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[maprotilin] 3.97 1.48 6.0 5.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[maprotilin] 3.87 1.85 6.0 15.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](1).[maprotilin] 3.51 1.30 6.0 37.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[b-Cyclodextrin](2).[Cinnarizine 2HCl] 3.46 2.31 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[b-Cyclodextrin](1).[Cinnarizine 2HCl] 2.32 1.24 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[b-Cyclodextrin](1).[fenoprofen calcium dihydrate] 2.98 1.97 7.4 25.0 UV-vis spectroscopy David Diaz 1999
[b-Cyclodextrin](1).[fenoprofen calcium dihydrate] 3.00 2.16 7.4 25.0 Fluorescence spectroscopy David Diaz 1999
[b-Cyclodextrin](1).[L-tyrosine ] 1.68 0.70 7.0 20.0 Fluorescence spectroscopy Frank V. Bright 1996
[b-Cyclodextrin](1).[YIGSR ] 2.35 1.00 7.0 20.0 Fluorescence spectroscopy Frank V. Bright 1996
[b-Cyclodextrin](1).[YGGFL] 2.09 1.18 7.0 20.0 Fluorescence spectroscopy Frank V. Bright 1996
[b-Cyclodextrin](1).[anthraquinone] 2.46 7.0 25.0 Osteryoung square wave voltammetry Hu-Lin Li 1996
[b-Cyclodextrin](1).[anthraquinone] 2.35 7.0 25.0 UV-vis spectroscopy Hu-Lin Li 1996
[b-Cyclodextrin](1).[N-methyil-p-(p-dimethylaminophenyl)-pyridinium iodide] 2.61 7.0 27.0 Fluorescence spectroscopy Michael I. Knyazhansky 1993
[b-Cyclodextrin](1).[1NpMeOH] 2.38 Fluorescence spectroscopy Akira Harada 2006
[b-Cyclodextrin](1).[2NpMeOH] 2.87 Fluorescence spectroscopy Akira Harada 2006
[b-Cyclodextrin](1).[1NpA/AAm (22)] 2.15 Fluorescence spectroscopy Akira Harada 2006
[b-Cyclodextrin](1).[1NpA/AAm (64)] 1.85 Fluorescence spectroscopy Akira Harada 2006
[b-Cyclodextrin](1).[ampicillin] 3.68 2.70 1.2 25.0 Microcalorimetry Hatsumi Aki 2004
[b-Cyclodextrin](1).[ampicillin] 3.06 2.30 4.0 25.0 Microcalorimetry Hatsumi Aki 2004
[b-Cyclodextrin](1).[ampicillin] 3.09 2.60 6.0 25.0 Microcalorimetry Hatsumi Aki 2004
[b-Cyclodextrin](1).[2NpA/AAm (52)] 2.36 Fluorescence spectroscopy Akira Harada 2006
[b-Cyclodextrin](1).[2NpA/AAm (73)] 2.20 Fluorescence spectroscopy Akira Harada 2006
[b-Cyclodextrin](1).[adamantane carboxylate] 4.70 6.9 30.0 Microcalorimetry Daniel Harries 2005
[b-Cyclodextrin](1).[adamantane carboxylate] 5.00 10.0 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](1).[tryptophan] 1.77 0.70 7.0 30.0 NMR spectroscopy Akira Harada 2006
[b-Cyclodextrin](1).[tryptophan] 1.70 NMR spectroscopy Ronald Breslow 2003
[b-Cyclodextrin](1).[poly(N-methacryloyltryptophan)] 1.73 0.48 7.0 25.0 Fluorescence spectroscopy Akira Harada 2006
[b-Cyclodextrin](1).[poly(N-methacryloyltryptophan)] 1.92 0.48 7.0 30.0 NMR spectroscopy Akira Harada 2006
[b-Cyclodextrin](1).[paclitaxel] 2.53 7.0 25.0 HPLC-method Massimo Fresta 2002
[b-Cyclodextrin](1).[paclitaxel] 2.29 7.0 37.0 HPLC-method Massimo Fresta 2002
[b-Cyclodextrin](1).[paclitaxel] 1.80 7.0 45.0 HPLC-method Massimo Fresta 2002
[b-Cyclodextrin](1).[crystal violet (planar)] 3.49 7.0 25.0 UV-vis spectroscopy L. Garcia-Rio 2005
[b-Cyclodextrin](1).[crystal violet (pyramidal)] 2.96 7.0 25.0 UV-vis spectroscopy L. Garcia-Rio 2005
[b-Cyclodextrin](1).[pyronine Y] 2.56 2.74 4.0 21.0 Fluorescence Correlation Spectroscopy Wajih Al-Soufi 2005
[b-Cyclodextrin](1).[R-3-T3] 2.28 George W. Gokel 2003
[b-Cyclodextrin](1).[S-3-T3] 2.24 George W. Gokel 2003
[b-Cyclodextrin](1).[R-5-T3] 2.73 George W. Gokel 2003
[b-Cyclodextrin](1).[S-5-T3] 2.42 George W. Gokel 2003
[b-Cyclodextrin](1).[R-7-T3] 2.49 George W. Gokel 2003
[b-Cyclodextrin](1).[pyronine B] 3.08 2.95 4.0 21.0 Fluorescence Correlation Spectroscopy Wajih Al-Soufi 2005
[b-Cyclodextrin](1).[S-7-T3] 2.55 George W. Gokel 2003
[b-Cyclodextrin](1).[R-8-T3] 2.67 George W. Gokel 2003
[b-Cyclodextrin](1).[S-8-T3] 2.78 George W. Gokel 2003
[b-Cyclodextrin](1).[R-9-T3] 2.67 George W. Gokel 2003
[b-Cyclodextrin](1).[S-9-T3] 2.88 George W. Gokel 2003
[b-Cyclodextrin](1).[R-1-T3] 2.47 George W. Gokel 2003
[b-Cyclodextrin](1).[S-1-T3] 2.55 George W. Gokel 2003
[b-Cyclodextrin](1).[R-11-T3] 2.61 George W. Gokel 2003
[b-Cyclodextrin](1).[S-11-T3] 2.82 George W. Gokel 2003
[b-Cyclodextrin](1).[R-12-T3] 2.53 George W. Gokel 2003
[b-Cyclodextrin](1).[chlorogenic acid] 2.67 1.41 7.0 25.0 Fluorescence Spectroscopy and Ferric Reducing/Antioxidant Power Assay (FRAP) techniques Emilio Alvarez-Parrilla 2005
[b-Cyclodextrin](1).[S-12-T3] 2.61 George W. Gokel 2003
[b-Cyclodextrin](1).[R-13-T3] 1.78 0.11 George W. Gokel 2003
[b-Cyclodextrin](1).[S-13-T3] 1.83 0.15 George W. Gokel 2003
[b-Cyclodextrin](1).[R-14-T3] 1.10 -0.30 George W. Gokel 2003
[b-Cyclodextrin](1).[S-14-T3] 1.23 -0.30 George W. Gokel 2003
[b-Cyclodextrin](1).[R-15-T3] 2.10 0.30 George W. Gokel 2003
[b-Cyclodextrin](1).[S-15-T3] 2.11 0.30 George W. Gokel 2003
[b-Cyclodextrin](1).[R-16-T3] 1.85 0.60 George W. Gokel 2003
[b-Cyclodextrin](1).[S-16-T3] 1.84 0.48 George W. Gokel 2003
[b-Cyclodextrin](1).[R-17-T3] 1.04 0.30 George W. Gokel 2003
[b-Cyclodextrin](1).[rutin] 2.35 1.15 7.0 25.0 Fluorescence Spectroscopy and Ferric Reducing/Antioxidant Power Assay (FRAP) techniques Emilio Alvarez-Parrilla 2005
[b-Cyclodextrin](1).[S-17-T3] 1.08 George W. Gokel 2003
[b-Cyclodextrin](1).[R-18-T3] 2.00 George W. Gokel 2003
[b-Cyclodextrin](1).[S-18-T3] 2.04 George W. Gokel 2003
[b-Cyclodextrin](1).[R-19-T3] 2.17 0.60 George W. Gokel 2003
[b-Cyclodextrin](1).[S-19-T3] 2.17 0.60 George W. Gokel 2003
[b-Cyclodextrin](1).[R-2-T3] 2.49 0.30 George W. Gokel 2003
[b-Cyclodextrin](1).[S-2-T3] 2.45 0.30 George W. Gokel 2003
[b-Cyclodextrin](1).[R-21-T3] 2.59 0.60 George W. Gokel 2003
[b-Cyclodextrin](1).[S-21-T3] 2.56 0.60 George W. Gokel 2003
[b-Cyclodextrin](1).[R-22-T3] 2.82 0.78 George W. Gokel 2003
[b-Cyclodextrin](1).[S-22-T3] 2.76 0.60 George W. Gokel 2003
[b-Cyclodextrin](1).[R-39-T3] 1.92 0.30 George W. Gokel 2003
[b-Cyclodextrin](1).[S-39-T3] 1.93 0.30 George W. Gokel 2003
[b-Cyclodextrin](1).[R-45-T3] 1.85 0.30 George W. Gokel 2003
[b-Cyclodextrin](1).[S-45-T3] 1.87 0.30 George W. Gokel 2003
[b-Cyclodextrin](1).[cimetidine] 2.63 6.8 25.0 HPLC-method Alamdar Ashnagar 2005
[b-Cyclodextrin](1).[R-7-T5] 2.36 George W. Gokel 2003
[b-Cyclodextrin](1).[S-7-T5] 2.48 George W. Gokel 2003
[b-Cyclodextrin](1).[R-8-T5] 2.52 George W. Gokel 2003
[b-Cyclodextrin](1).[S-8-T5] 2.40 George W. Gokel 2003
[b-Cyclodextrin](1).[R-9-T5] 3.04 George W. Gokel 2003
[b-Cyclodextrin](1).[2-(p-tolyl)ethylamine] 2.14 6.8 25.0 HPLC-method Alamdar Ashnagar 2005
[b-Cyclodextrin](1).[S-9-T5] 3.00 George W. Gokel 2003
[b-Cyclodextrin](1).[R-1-T5] 1.80 George W. Gokel 2003
[b-Cyclodextrin](1).[S-1-T5] 1.72 George W. Gokel 2003
[b-Cyclodextrin](1).[R-11-T5] 2.52 0.48 George W. Gokel 2003
[b-Cyclodextrin](1).[S-11-T5] 2.52 0.48 George W. Gokel 2003
[b-Cyclodextrin](1).[R-12-T5] 1.04 0.30 George W. Gokel 2003
[b-Cyclodextrin](1).[S-12-T5] 0.95 0.30 George W. Gokel 2003
[b-Cyclodextrin](1).[R-13-T5] 1.78 0.48 George W. Gokel 2003
[b-Cyclodextrin](1).[S-13-T5] 1.86 0.30 George W. Gokel 2003
[b-Cyclodextrin](1).[R-14-T5] 1.94 George W. Gokel 2003
[b-Cyclodextrin](1).[S-14-T5] 1.92 George W. Gokel 2003
[b-Cyclodextrin](1).[R-15-T5] 2.89 1.30 George W. Gokel 2003
[b-Cyclodextrin](1).[S-15-T5] 2.91 1.00 George W. Gokel 2003
[b-Cyclodextrin](1).[R-16-T5] 1.81 1.04 George W. Gokel 2003
[b-Cyclodextrin](1).[S-16-T5] 1.74 0.70 George W. Gokel 2003
[b-Cyclodextrin](1).[R-17-T5] 1.94 0.78 George W. Gokel 2003
[b-Cyclodextrin](1).[S-17-T5] 1.86 0.60 George W. Gokel 2003
[b-Cyclodextrin](1).[R-1-T7] 2.36 George W. Gokel 2003
[b-Cyclodextrin](1).[S-1-T7] 2.45 George W. Gokel 2003
[b-Cyclodextrin](1).[R-2-T7] 2.53 0.78 George W. Gokel 2003
[b-Cyclodextrin](1).[S-2-T7] 2.49 0.78 George W. Gokel 2003
[b-Cyclodextrin](1).[R-5-T7] 2.65 1.32 George W. Gokel 2003
[b-Cyclodextrin](1).[S-5-T7] 2.96 1.73 George W. Gokel 2003
[b-Cyclodextrin](1).[R-6-T7] 2.42 George W. Gokel 2003
[b-Cyclodextrin](1).[S-6-T7] 2.53 George W. Gokel 2003
[b-Cyclodextrin](1).[R-9-T7] 1.45 George W. Gokel 2003
[b-Cyclodextrin](1).[(P)-1,12-dimethylbenzo[c]phenantrene-5,8-dicarboxylic acid] 4.27 3.23 7.0 25.0 NMR spectroscopy George W. Gokel 2003
[b-Cyclodextrin](1).[(M)-1,12-dimethylbenzo[c]phenantrene-5,8-dicarboxylic acid] 3.34 2.00 7.0 25.0 NMR spectroscopy George W. Gokel 2003
[b-Cyclodextrin](1).[R-C8] 2.75 1.48 7.0 25.0 NMR spectroscopy George W. Gokel 2003
[b-Cyclodextrin](1).[S-C8] 2.64 1.48 7.0 25.0 NMR spectroscopy George W. Gokel 2003
[b-Cyclodextrin](1).[R-C1] 2.86 1.85 7.0 25.0 NMR spectroscopy George W. Gokel 2003
[b-Cyclodextrin](1).[S-C1] 2.69 1.78 7.0 25.0 NMR spectroscopy George W. Gokel 2003
[b-Cyclodextrin](1).[melarsoprol] 3.97 HPLC method Stéphane Gibaud 2002
[b-Cyclodextrin](1).[pyridinephenolates] 2.21 1.70 7.0 25.0 UV-vis spectroscopy Marcos Caroli Rezende 2006
[b-Cyclodextrin](1).[pyrocatechol] 2.61 25.0 UV-vis spectroscopy Jun-Min Wan 2006
[b-Cyclodextrin](1).[pyrocatechol] 2.49 30.0 UV-vis spectroscopy Jun-Min Wan 2006
[b-Cyclodextrin](1).[pyrocatechol] 2.33 35.0 UV-vis spectroscopy Jun-Min Wan 2006
[b-Cyclodextrin](1).[pyrocatechol] 2.18 40.0 UV-vis spectroscopy Jun-Min Wan 2006
[b-Cyclodextrin](1).[hydroquinone] 2.63 25.0 UV-vis spectroscopy Jun-Min Wan 2006
[b-Cyclodextrin](1).[hydroquinone] 2.53 30.0 UV-vis spectroscopy Jun-Min Wan 2006
[b-Cyclodextrin](1).[hydroquinone] 2.41 35.0 UV-vis spectroscopy Jun-Min Wan 2006
[b-Cyclodextrin](1).[hydroquinone] 2.27 40.0 UV-vis spectroscopy Jun-Min Wan 2006
[b-Cyclodextrin](1).[resorcinol] 2.66 25.0 UV-vis spectroscopy Jun-Min Wan 2006
[b-Cyclodextrin](1).[resorcinol] 2.56 30.0 UV-vis spectroscopy Jun-Min Wan 2006
[b-Cyclodextrin](1).[resorcinol] 2.47 35.0 UV-vis spectroscopy Jun-Min Wan 2006
[b-Cyclodextrin](1).[resorcinol] 2.29 40.0 UV-vis spectroscopy Jun-Min Wan 2006
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinone derivative C-1] 2.78 1.70 1.0 25.0 UV-vis spectroscopy Mekki Kadri 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinone derivative C-1] 2.79 1.60 4.3 25.0 UV-vis spectroscopy Mekki Kadri 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinone derivative C-1] 4.04 1.90 7.4 25.0 UV-vis spectroscopy Mekki Kadri 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinone derivative C-1] 4.04 1.00 8.5 25.0 UV-vis spectroscopy Mekki Kadri 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinone derivative C-1] 3.98 1.85 11.0 25.0 UV-vis spectroscopy Mekki Kadri 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinone derivative C-2] 3.40 2.18 1.0 25.0 UV-vis spectroscopy Mekki Kadri 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinone derivative C-2] 3.18 2.30 4.3 25.0 UV-vis spectroscopy Mekki Kadri 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinone derivative C-2] 4.45 2.00 7.4 25.0 UV-vis spectroscopy Mekki Kadri 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinone derivative C-2] 4.42 2.18 8.5 25.0 UV-vis spectroscopy Mekki Kadri 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinone derivative C-2] 4.17 2.00 11.0 25.0 UV-vis spectroscopy Mekki Kadri 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinone derivative C-3] 2.81 1.48 1.0 25.0 UV-vis spectroscopy Mekki Kadri 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinone derivative C-3] 2.99 1.85 4.3 25.0 UV-vis spectroscopy Mekki Kadri 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinone derivative C-3] 4.20 2.04 7.4 25.0 UV-vis spectroscopy Mekki Kadri 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinone derivative C-3] 4.18 1.70 8.5 25.0 UV-vis spectroscopy Mekki Kadri 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinone derivative C-3] 4.08 1.85 11.0 25.0 UV-vis spectroscopy Mekki Kadri 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinone derivative C-4] 2.65 1.54 1.0 25.0 UV-vis spectroscopy Mekki Kadri 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinone derivative C-4] 2.89 1.00 4.3 25.0 UV-vis spectroscopy Mekki Kadri 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinone derivative C-4] 4.02 1.70 7.4 25.0 UV-vis spectroscopy Mekki Kadri 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinone derivative C-4] 4.06 1.70 8.5 25.0 UV-vis spectroscopy Mekki Kadri 2005
[b-Cyclodextrin](1).[N-sulfamoyloxazolidinone derivative C-4] 3.98 1.40 11.0 25.0 UV-vis spectroscopy Mekki Kadri 2005
[b-Cyclodextrin](1).[sec-Butanol] 1.19 25.0 Toshio Shinbo 2004
[b-Cyclodextrin](1).[n-Butanol] 1.22 25.0 Toshio Shinbo 2004
[b-Cyclodextrin](1).[iso-Butanol] 1.62 25.0 Toshio Shinbo 2004
[b-Cyclodextrin](1).[tert-Butanol] 1.68 25.0 Toshio Shinbo 2004
[b-Cyclodextrin](1).[butyric acid] 2.08 1.76 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[b-Cyclodextrin](1).[isobutyric acid] 2.30 0.38 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[b-Cyclodextrin](1).[valeric acid] 2.28 1.10 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[b-Cyclodextrin](1).[isovaleric acid] 2.31 1.73 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[b-Cyclodextrin](1).[succinic acid] 1.33 1.21 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[b-Cyclodextrin](1).[succinic acid] 1.29 0.65 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[b-Cyclodextrin](1).[cadaverine] 1.62 0.32 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[b-Cyclodextrin](1).[phenantrene] 3.09 7.0 22.0 UV/VIS spectrometry Khalil Hanna 2004
[b-Cyclodextrin](1).[putrescine] 1.59 1.06 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[b-Cyclodextrin](1).[pyridine ] 1.73 0.26 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[b-Cyclodextrin](1).[3-methyl-pyridine] 1.51 0.41 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[b-Cyclodextrin](1).[diphenylamine] 2.34 1.09 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[b-Cyclodextrin](1).[hydrogen sulfide] 0.87 0.34 22.0 HS-GCMS Daniel W. Armstrong 2006
[b-Cyclodextrin](1).[methanethiol] 0.23 -0.33 22.0 HS-GCMS Daniel W. Armstrong 2006
[b-Cyclodextrin](1).[dimethyl sulfide] 1.24 0.50 22.0 HS-GCMS Daniel W. Armstrong 2006
[b-Cyclodextrin](1).[phenyl acetate] 2.03 0.72 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[b-Cyclodextrin](1).[m-cresol] 2.10 1.44 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[b-Cyclodextrin](1).[m-cresol] 1.90 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[phenol ] 1.78 0.76 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[b-Cyclodextrin](1).[camphanate ester of 2,3-diazabicyclo[2.2.2]oct-2-ene] 3.08 2.26 7.0 25.0 NMR spectroscopy Werner M. Nau 2005
[b-Cyclodextrin](2).[camphanate ester of 2,3-diazabicyclo[2.2.2]oct-2-ene] 2.11 1.00 7.0 25.0 NMR spectroscopy Werner M. Nau 2005
[b-Cyclodextrin](1).[indole] 2.22 -0.40 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[b-Cyclodextrin](1).[skatole] 2.21 0.11 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[b-Cyclodextrin](1).[dodecanol] 2.00 1.53 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[b-Cyclodextrin](1).[tatradecanol] 2.30 1.40 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[b-Cyclodextrin](1).[polyamide acids] 4.72 3.30 7.0 25.0 Electrospray Ionization Mass Spectrometry Gu Yuan 2006
[b-Cyclodextrin](1).[sodium 6-(p-toluidino)-2-naphthalenesulfonate] 3.56 7.2 25.0 Fluorescence spectroscopy Liu Yu 2004
[b-Cyclodextrin](1).[ammonium 8-anilino-1-naphthalenesulfonate] 2.01 7.2 25.0 Fluorescence spectroscopy Liu Yu 2004
[b-Cyclodextrin](1).[ammonium 8-anilino-1-naphthalenesulfonate] 2.01 7.2 25.0 UV-vis spectroscopy Yu Liu 2003
[b-Cyclodextrin](1).[hexanoic acid] 2.59 7.0 50.0 NMR spectroscopy Jose J. C. Teixeira-Dias 2004
[b-Cyclodextrin](1).[decanoic acid] 2.93 7.0 50.0 NMR spectroscopy Jose J. C. Teixeira-Dias 2004
[b-Cyclodextrin](1).[NO3-] -0.59 7.0 50.0 NMR spectroscopy Jose J. C. Teixeira-Dias 2004
[b-Cyclodextrin](1).[Cl-] -0.34 7.0 50.0 NMR spectroscopy Jose J. C. Teixeira-Dias 2004
[b-Cyclodextrin](1).[(+)-amido tetralins] 1.96 7.0 40.0 HPLC method C. Vaccher 2003
[b-Cyclodextrin](1).[(-)-amido tetralins] 1.90 7.0 40.0 HPLC method C. Vaccher 2003
[b-Cyclodextrin](1).[S-amido tetralins] 2.06 7.0 40.0 HPLC method C. Vaccher 2003
[b-Cyclodextrin](1).[R-amido tetralins] 2.00 7.0 40.0 HPLC method C. Vaccher 2003
[b-Cyclodextrin](1).[prazosin hydrochloride] 1.47 0.40 7.0 25.0 UV-vis spectroscopy Longxiao Liu 2006
[b-Cyclodextrin](1).[di-2-(1-adamantyl)ethyl hydrogenophosphate in anionic form] 5.36 7.0 Carlos Jaime 2006
[b-Cyclodextrin](2).[di-2-(1-adamantyl)ethyl hydrogenophosphate in anionic form] 3.64 7.0 Carlos Jaime 2006
[b-Cyclodextrin](1).[sodium 6-toluidino-2-naphthalenesulfonate] 3.57 7.2 25.0 Fluorescence spectroscopy Yu Liu 2004
[b-Cyclodextrin](1).[tetrathiafulvalene] 4.04 3.30 6.4 20.0 Fluorescence spectroscopy Philippe Hapiot 2006
[b-Cyclodextrin](1).[p-nitrobenzene derivative 1] 3.03 1.70 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[b-Cyclodextrin](1).[p-nitrobenzene derivative 2] 2.85 1.40 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[b-Cyclodextrin](1).[p-nitrobenzene derivative 3] 2.96 1.70 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[b-Cyclodextrin](1).[p-nitrobenzene derivative 4] 2.77 1.48 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[b-Cyclodextrin](1).[p-nitrobenzene derivative 5] 2.24 1.40 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[b-Cyclodextrin](1).[p-nitrobenzene derivative 6] 3.16 1.81 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[b-Cyclodextrin](1).[p-nitrobenzene derivative 7] 2.88 1.48 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[b-Cyclodextrin](1).[p-nitrobenzene derivative 8] 3.11 1.60 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[b-Cyclodextrin](1).[p-nitrobenzene derivative 9] 3.42 1.54 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[b-Cyclodextrin](1).[xanthon-1] 1.21 10.0 25.0 Capillary electrophoresis Huwei Liu 2003
[b-Cyclodextrin](1).[p-nitrobenzene derivative 11] 4.24 2.49 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[b-Cyclodextrin](1).[p-nitrobenzene derivative 12] 2.54 1.65 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[b-Cyclodextrin](1).[p-nitrobenzene derivative 13] 2.82 1.70 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[b-Cyclodextrin](1).[R-rivastigmine] 2.26 2.5 25.0 Capillary electrophoresis Ernst Kenndler 2005
[b-Cyclodextrin](1).[xanthon-2] 2.39 10.0 25.0 Capillary electrophoresis Huwei Liu 2003
[b-Cyclodextrin](1).[norharmane] 1.54 7.0 Fluorescence spectroscopy Nitin Chattopadhyay 2005
[b-Cyclodextrin](2).[norharmane] 4.72 7.0 Fluorescence spectroscopy Nitin Chattopadhyay 2005
[b-Cyclodextrin](1).[xanthon-3] 2.65 10.0 25.0 Capillary electrophoresis Huwei Liu 2003
[b-Cyclodextrin](1).[4-chlorophenol] 2.48 7.0 22.0 Circular dichroism spectroscopy Sandra Monti 2005
[b-Cyclodextrin](1).[4-chlorophenol] 2.30 5.0 25.0 Capillary electrophoresis Thomas Le Saux 2006
[b-Cyclodextrin](1).[4-chlorophenol] 2.20 5.0 25.0 Microchip electrophoresis Thomas Le Saux 2006
[b-Cyclodextrin](1).[4-chlorophenol] 2.63 1.83 2.0 20.0 UV-vis spectroscopy Miguel A. Garcia-Garibay 2001
[b-Cyclodextrin](1).[4-chlorophenol] 2.62 1.20 7.0 20.0 NMR spectroscopy Miguel A. Garcia-Garibay 2001
[b-Cyclodextrin](1).[4-chlorophenol] 2.57 23.0 NIR spectroscopy Chieu D. Tran 1995
[b-Cyclodextrin](1).[styrene] 2.54 Kasi Pitchumani 2005
[b-Cyclodextrin](1).[styrene] 4.50 3.53 20.0 UV/VIS spectroscopy S. Divakar 2000
[b-Cyclodextrin](1).[methyl cinnamate] 2.36 Kasi Pitchumani 2005
[b-Cyclodextrin](1).[phenylacetylene] 2.42 Kasi Pitchumani 2005
[b-Cyclodextrin](1).[allylbenzene] 2.50 Kasi Pitchumani 2005
[b-Cyclodextrin](1).[xanthon-4] 2.65 10.0 25.0 Capillary electrophoresis Huwei Liu 2003
[b-Cyclodextrin](1).[E-4-tertbutylphenyl-4' -oxyazobenzene] 5.09 4.08 10.0 25.0 UV-vis spectroscopy Stephen F. Lincoln 2005
[b-Cyclodextrin](2).[E-4-tertbutylphenyl-4' -oxyazobenzene] 4.09 2.78 10.0 25.0 UV-vis spectroscopy Stephen F. Lincoln 2005
[b-Cyclodextrin](1).[gliquidone] 2.81 7.0 25.0 UV-vis spectroscopy M.I. La Rotonda 2004
[b-Cyclodextrin](1).[gliquidone] 2.51 1.5 25.0 UV-vis spectroscopy M.I. La Rotonda 2004
[b-Cyclodextrin](1).[gliquidone] 2.78 4.5 25.0 UV-vis spectroscopy M.I. La Rotonda 2004
[b-Cyclodextrin](1).[gliquidone] 3.27 7.4 25.0 UV-vis spectroscopy M.I. La Rotonda 2004
[b-Cyclodextrin](2).[gliquidone] 2.20 7.4 25.0 UV-vis spectroscopy M.I. La Rotonda 2004
[b-Cyclodextrin](1).[p-dimethylaminobenzonitrile] 2.40 0.11 7.0 20.0 Fluorescence spectroscopy Sandra Monti 2003
[b-Cyclodextrin](1).[p-dimethylaminobenzonitrile] 2.65 0.15 7.0 20.0 Triplet–triplet absorption spectroscopy Sandra Monti 2003
[b-Cyclodextrin](1).[p-dimethylaminobenzonitrile] 2.18 0.04 7.0 20.0 UV-vis spectroscopy Sandra Monti 2003
[b-Cyclodextrin](1).[p-dimethylaminobenzonitrile] 2.77 0.04 7.0 20.0 Circular dichroism spectroscopy Sandra Monti 2003
[b-Cyclodextrin](2).[p-dimethylaminobenzonitrile] 8.69 0.08 7.0 20.0 Fluorescence spectroscopy Sandra Monti 2003
[b-Cyclodextrin](2).[p-dimethylaminobenzonitrile] 9.08 0.17 7.0 20.0 UV-vis spectroscopy Sandra Monti 2003
[b-Cyclodextrin](1).[xanthon-5] 2.25 10.0 25.0 Capillary electrophoresis Huwei Liu 2003
[b-Cyclodextrin](1).[xanthon-6] 2.82 10.0 25.0 Capillary electrophoresis Huwei Liu 2003
[b-Cyclodextrin](1).[L-Phe-L-Phe] 1.54 Capillary electrophoresis Bezhan Chankvetadze 2004
[b-Cyclodextrin](1).[D-Phe-D-Phe] 1.64 Capillary electrophoresis Bezhan Chankvetadze 2004
[b-Cyclodextrin](1).[L-Ala-L-Tyr] 2.10 Capillary electrophoresis Bezhan Chankvetadze 2004
[b-Cyclodextrin](1).[D-Ala-D-Tyr] 2.24 Capillary electrophoresis Bezhan Chankvetadze 2004
[b-Cyclodextrin](1).[L-Asp-L-PheOMe] 1.58 Capillary electrophoresis Bezhan Chankvetadze 2004
[b-Cyclodextrin](1).[D-Asp-D-PheOMe] 1.66 Capillary electrophoresis Bezhan Chankvetadze 2004
[b-Cyclodextrin](1).[xanthon-7] 0.87 10.0 25.0 Capillary electrophoresis Huwei Liu 2003
[b-Cyclodextrin](1).[adamantanecarboxylic acid] 4.60 7.4 25.0 Isothermal titration calorymetry Antonio Vargas-Berenguel 2003
[b-Cyclodextrin](1).[adamantanecarboxylic acid] 3.15 25.0 NMR spectroscopy Zdenek Tosner 2006
[b-Cyclodextrin](1).[adamantanecarboxylic acid] 4.28 8.5 25.0 microcalorimetry, pH potentiometry Maurice R. Eftink 1985
[b-Cyclodextrin](1).[adamantanecarboxylic acid] 4.52 7.22 25.0 microcalorimetry, pH potentiometry Maurice R. Eftink 1985
[b-Cyclodextrin](1).[adamantanecarboxylic acid] 5.46 4.08 25.0 microcalorimetry, pH potentiometry Maurice R. Eftink 1985
[b-Cyclodextrin](1).[salicylidine-3,4,7-methyl amine] 2.83 7.0 23.0 Fluorescence spectroscopy S. Mukherjee 2005
[b-Cyclodextrin](1).[meso-tetrakis(4-sulfonatophenyl)porphyrin] 4.49 3.60 7.0 25.0 Isothermal titration calorymetry Anthony L. Spek 2004
[b-Cyclodextrin](1).[xanthone] 3.04 2.30 7.0 25.0 Induced circular dichroism B. Mayer 1999
[b-Cyclodextrin](1).[xanthone] 3.04 2.30 spectroscopy Cornelia Bohne 2001
[b-Cyclodextrin](1).[xanthone] 1.78 1.00 25.0 absorption spectroscopy Cornelia Bohne 2001
[b-Cyclodextrin](1).[fluorenone] 2.65 1.70 7.0 25.0 Induced circular dichroism B. Mayer 1999
[b-Cyclodextrin](1).[b-lapachone] 3.09 1.00 7.4 25.0 UV-vis spectroscopy Jinming Gao 2003
[b-Cyclodextrin](1).[b-lapachone] 3.04 1.78 7.4 25.0 Fluorescence spectroscopy Jinming Gao 2003
[b-Cyclodextrin](1).[b-lapachone] 2.89 1.72 7.0 25.0 NMR spectroscopy Jinming Gao 2003
[b-Cyclodextrin](1).[xanthon-8] 2.57 10.0 25.0 Capillary electrophoresis Huwei Liu 2003
[b-Cyclodextrin](1).[1-{[3-(6,7-dihydro-1-methyl-7-oxo-3-propyl-1H-pyrazolo[4,3-d] pyrimidin-5-yl)-4-ethoxyphenyl] sulfonyl}-4-methylpiperazine] 2.18 0.70 8.7 30.0 UV-vis spectroscopy Mahmoud M. Al Omari 2006
[b-Cyclodextrin](1).[1-{[3-(6,7-dihydro-1-methyl-7-oxo-3-propyl-1H-pyrazolo[4,3-d] pyrimidin-5-yl)-4-ethoxyphenyl] sulfonyl}-4-methylpiperazine] 2.23 1.48 7.0 30.0 UV-vis spectroscopy Mahmoud M. Al Omari 2006
[b-Cyclodextrin](1).[1-{[3-(6,7-dihydro-1-methyl-7-oxo-3-propyl-1H-pyrazolo[4,3-d] pyrimidin-5-yl)-4-ethoxyphenyl] sulfonyl}-4-methylpiperazine] 1.23 0.60 3.6 30.0 UV-vis spectroscopy Mahmoud M. Al Omari 2006
[b-Cyclodextrin](1).[1-{[3-(6,7-dihydro-1-methyl-7-oxo-3-propyl-1H-pyrazolo[4,3-d] pyrimidin-5-yl)-4-ethoxyphenyl] sulfonyl}-4-methylpiperazine] 1.93 1.00 6.7 30.0 UV-vis spectroscopy Mahmoud M. Al Omari 2006
[b-Cyclodextrin](1).[1-{[3-(6,7-dihydro-1-methyl-7-oxo-3-propyl-1H-pyrazolo[4,3-d] pyrimidin-5-yl)-4-ethoxyphenyl] sulfonyl}-4-methylpiperazine] 2.15 0.60 8.2 30.0 UV-vis spectroscopy Mahmoud M. Al Omari 2006
[b-Cyclodextrin](1).[1-{[3-(6,7-dihydro-1-methyl-7-oxo-3-propyl-1H-pyrazolo[4,3-d] pyrimidin-5-yl)-4-ethoxyphenyl] sulfonyl}-4-methylpiperazine] 1.62 0.90 12.1 30.0 UV-vis spectroscopy Mahmoud M. Al Omari 2006
[b-Cyclodextrin](1).[1-{[3-(6,7-dihydro-1-methyl-7-oxo-3-propyl-1H-pyrazolo[4,3-d] pyrimidin-5-yl)-4-ethoxyphenyl] sulfonyl}-4-methylpiperazine] 2.30 1.36 8.7 21.0 UV-vis spectroscopy Mahmoud M. Al Omari 2006
[b-Cyclodextrin](1).[1-{[3-(6,7-dihydro-1-methyl-7-oxo-3-propyl-1H-pyrazolo[4,3-d] pyrimidin-5-yl)-4-ethoxyphenyl] sulfonyl}-4-methylpiperazine] 2.26 0.95 8.7 25.5 UV-vis spectroscopy Mahmoud M. Al Omari 2006
[b-Cyclodextrin](1).[1-{[3-(6,7-dihydro-1-methyl-7-oxo-3-propyl-1H-pyrazolo[4,3-d] pyrimidin-5-yl)-4-ethoxyphenyl] sulfonyl}-4-methylpiperazine] 2.18 0.70 8.7 31.0 UV-vis spectroscopy Mahmoud M. Al Omari 2006
[b-Cyclodextrin](1).[1-{[3-(6,7-dihydro-1-methyl-7-oxo-3-propyl-1H-pyrazolo[4,3-d] pyrimidin-5-yl)-4-ethoxyphenyl] sulfonyl}-4-methylpiperazine] 2.16 0.85 8.7 37.5 UV-vis spectroscopy Mahmoud M. Al Omari 2006
[b-Cyclodextrin](1).[1-{[3-(6,7-dihydro-1-methyl-7-oxo-3-propyl-1H-pyrazolo[4,3-d] pyrimidin-5-yl)-4-ethoxyphenyl] sulfonyl}-4-methylpiperazine] 2.05 1.04 8.7 45.0 UV-vis spectroscopy Mahmoud M. Al Omari 2006
[b-Cyclodextrin](1).[7-hydroxyquinoline] 1.94 7.0 25.0 UV-vis spectroscopy Du-Jeon Jang 2005
[b-Cyclodextrin](1).[benzocaine] 2.74 1.62 7.0 25.0 UV-vis spectroscopy Eneida de Paula 2005
[b-Cyclodextrin](1).[valdecoxib] 2.17 6.8 25.0 UV-vis spectroscopy Tayade Pralhad 2005
[b-Cyclodextrin](1).[((S)-(+)-6-methoxy-a-methyl-2-naphthaleneacetic acid] 3.26 7.4 25.0 Fluorescence spectroscopy Reynaldo Villalonga 2006
[b-Cyclodextrin](1).[xanthon-9] 2.59 10.0 25.0 Capillary electrophoresis Huwei Liu 2003
[b-Cyclodextrin](1).[tolfenamic acid] 2.66 7.0 25.0 HPLC-method E. Antoniadou-Vyza 2005
[b-Cyclodextrin](1).[tolfenamic acid] 2.47 7.0 30.0 HPLC-method E. Antoniadou-Vyza 2005
[b-Cyclodextrin](1).[tolfenamic acid] 2.37 7.0 37.0 HPLC-method E. Antoniadou-Vyza 2005
[b-Cyclodextrin](1).[tolfenamic acid] 2.26 7.0 45.0 HPLC-method E. Antoniadou-Vyza 2005
[b-Cyclodextrin](2).[ketoprofen] 2.57 9.0 30.0 HPLC-method E. Antoniadou-Vyza 2005
[b-Cyclodextrin](2).[ketoprofen] 2.57 10.0 37.0 HPLC-method E. Antoniadou-Vyza 2005
[b-Cyclodextrin](2).[ketoprofen] 2.56 11.0 45.0 HPLC-method E. Antoniadou-Vyza 2005
[b-Cyclodextrin](2).[ketoprofen] 2.55 12.0 52.0 HPLC-method E. Antoniadou-Vyza 2005
[b-Cyclodextrin](1).[fenoprofen] 3.68 2.60 2.0 20.0 Fluorescence spectroscopy Jana Sadecka 2005
[b-Cyclodextrin](1).[fenoprofen] 3.26 1.90 7.0 20.0 Fluorescence spectroscopy Jana Sadecka 2005
[b-Cyclodextrin](1).[dibenzofuran-2-carboxylic acid] 3.95 3.00 2.0 25.0 Fluorescence spectroscopy Gustavo González-Gaitano 2004
[b-Cyclodextrin](1).[dibenzofuran-2-carboxylic acid] 3.45 1.60 10.0 15.0 Fluorescence spectroscopy Gustavo González-Gaitano 2004
[b-Cyclodextrin](1).[dibenzofuran-2-carboxylic acid] 3.33 1.70 10.0 25.0 Fluorescence spectroscopy Gustavo González-Gaitano 2004
[b-Cyclodextrin](1).[dibenzofuran-2-carboxylic acid] 3.23 1.60 10.0 35.0 Fluorescence spectroscopy Gustavo González-Gaitano 2004
[b-Cyclodextrin](1).[dibenzofuran-2-carboxylic acid] 3.12 1.70 10.0 45.0 Fluorescence spectroscopy Gustavo González-Gaitano 2004
[b-Cyclodextrin](1).[dibenzofuran] 3.26 2.30 25.0 Fluorescence anisotropy titrations Gustavo González-Gaitano 2005
[b-Cyclodextrin](1).[xanthon-10] 2.97 10.0 25.0 Capillary electrophoresis Huwei Liu 2003
[b-Cyclodextrin](1).[2-hydroxydibenzofuran] 3.47 1.60 25.0 Fluorescence anisotropy titrations Gustavo González-Gaitano 2005
[b-Cyclodextrin](1).[dibenzofuran 2-carboxylate] 3.33 1.70 8.0 25.0 Fluorescence anisotropy titrations Gustavo González-Gaitano 2005
[b-Cyclodextrin](1).[rhodamine-B] 3.66 7.2 Fluorimetric titration Paolo Caliceti 2004
[b-Cyclodextrin](1).[2-naphtalenesulfonate] 2.60 5.0 25.0 Capillary electrophoresis Thomas Le Saux 2006
[b-Cyclodextrin](1).[2-naphtalenesulfonate] 2.40 5.0 25.0 Microchip electrophoresis Thomas Le Saux 2006
[b-Cyclodextrin](1).[phenol] 1.70 5.0 25.0 Capillary electrophoresis Thomas Le Saux 2006
[b-Cyclodextrin](1).[phenol] 1.90 5.0 25.0 Microchip electrophoresis Thomas Le Saux 2006
[b-Cyclodextrin](1).[phenol] 2.02 5.8 20.0 UV-vis spectroscopy; spectral displacement method D. Landy 2000
[b-Cyclodextrin](1).[phenol] 1.98 0.78 5.8 20.0 UV-vis spectroscopy D. Landy 2000
[b-Cyclodextrin](1).[phenol] 2.08 1.18 7.0 20.0 NMR spectroscopy D. Landy 2000
[b-Cyclodextrin](1).[phenol] 2.33 23.0 NIR spectroscopy Chieu D. Tran 1995
[b-Cyclodextrin](1).[phenol] 1.86 7.0 UV/VIS Spectroscopy Qing-Xhiang Guo 2001
[b-Cyclodextrin](1).[phenol] 1.98 0.62 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[phenol] 2.11 0.70 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[b-Cyclodextrin](1).[phenol] 1.60 0.30 Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[N-(1-adamantyl)acetamide] 4.56 3.48 7.0 25.0 Mass spectrometry, UV-vis spectrometry Willem Verboom 2005
[b-Cyclodextrin](1).[camphor] 3.78 2.78 7.0 27.0 NMR spectroscopy Svetlana Simova 2005
[b-Cyclodextrin](1).[(+)-menthone] 0.93 60.0 Gas chromatography Monika Asztemborska 2005
[b-Cyclodextrin](1).[(-)-menthone] 0.93 60.0 Gas chromatography Monika Asztemborska 2005
[b-Cyclodextrin](1).[(+)-isomnethone] 0.84 60.0 Gas chromatography Monika Asztemborska 2005
[b-Cyclodextrin](2).[(+)-isomnethone] 1.18 60.0 Gas chromatography Monika Asztemborska 2005
[b-Cyclodextrin](1).[(-)-isomnethone] 0.87 60.0 Gas chromatography Monika Asztemborska 2005
[b-Cyclodextrin](2).[(-)-isomnethone] 1.11 60.0 Gas chromatography Monika Asztemborska 2005
[b-Cyclodextrin](1).[(+)-fenchone] 1.08 60.0 Gas chromatography Monika Asztemborska 2005
[b-Cyclodextrin](2).[(+)-fenchone] 1.64 60.0 Gas chromatography Monika Asztemborska 2005
[b-Cyclodextrin](1).[(-)-fenchone] 1.00 60.0 Gas chromatography Monika Asztemborska 2005
[b-Cyclodextrin](2).[(-)-fenchone] 1.76 60.0 Gas chromatography Monika Asztemborska 2005
[b-Cyclodextrin](1).[(±)-pulegone] 0.95 60.0 Gas chromatography Monika Asztemborska 2005
[b-Cyclodextrin](1).[N-methyl-N-nitroso-p-toluenesulphonamide] 3.18 1.70 0.8 25.0 UV/VIS spectrometry Jorge Pérez-Juste 2006
[b-Cyclodextrin](1).[(+)-a-pinene] 1.81 60.0 Gas chromatography Monika Asztemborska 2005
[b-Cyclodextrin](1).[(-)-a-pinene] 1.81 60.0 Gas chromatography Monika Asztemborska 2005
[b-Cyclodextrin](1).[(+)-b-pinene] 2.00 60.0 Gas chromatography Monika Asztemborska 2005
[b-Cyclodextrin](1).[(-)-b-pinene] 2.00 60.0 Gas chromatography Monika Asztemborska 2005
[b-Cyclodextrin](1).[(+)-limonene] 0.94 60.0 Gas chromatography Monika Asztemborska 2005
[b-Cyclodextrin](1).[(-)-limonene] 0.94 60.0 Gas chromatography Monika Asztemborska 2005
[b-Cyclodextrin](1).[4-hydroxy-3,5-dimethoxybenzoic acid] 2.28 1.0 30.0 UV-vis spectroscopy N. Rajendiran 2006
[b-Cyclodextrin](1).[4-hydroxy-3,5-dimethoxybenzoic acid] 2.02 1.0 30.0 Fluorescence spectroscopy N. Rajendiran 2006
[b-Cyclodextrin](1).[4-hydroxy-3,5-dimethoxybenzoic acid] 2.31 7.0 30.0 UV-vis spectroscopy N. Rajendiran 2006
[b-Cyclodextrin](1).[4-hydroxy-3,5-dimethoxybenzoic acid] 2.04 7.0 30.0 Fluorescence spectroscopy N. Rajendiran 2006
[b-Cyclodextrin](1).[2-aminobenzoic acid] 2.28 1.0 30.0 UV-vis spectroscopy N. Rajendiran 2006
[b-Cyclodextrin](1).[2-aminobenzoic acid] 2.62 1.0 30.0 Fluorescence spectroscopy N. Rajendiran 2006
[b-Cyclodextrin](1).[2-aminobenzoic acid] 1.83 7.0 30.0 UV-vis spectroscopy N. Rajendiran 2006
[b-Cyclodextrin](1).[2-aminobenzoic acid] 1.98 7.0 30.0 Fluorescence spectroscopy N. Rajendiran 2006
[b-Cyclodextrin](1).[3-aminobenzoic acid] 2.33 7.0 30.0 UV-vis spectroscopy N. Rajendiran 2006
[b-Cyclodextrin](1).[3-aminobenzoic acid] 2.54 7.0 30.0 Fluorescence spectroscopy N. Rajendiran 2006
[b-Cyclodextrin](2).[3-aminobenzoic acid] -2.41 7.0 30.0 UV-vis spectroscopy N. Rajendiran 2006
[b-Cyclodextrin](2).[3-aminobenzoic acid] -2.19 7.0 30.0 Fluorescence spectroscopy N. Rajendiran 2006
[b-Cyclodextrin](1).[etilenglicol] -0.60 -1.30 0.8 25.0 UV/VIS spectrometry Jorge Pérez-Juste 2006
[b-Cyclodextrin](1).[4-CH3O-Phenol] 2.30 6.9 40.0 UV-vis spectroscopy Yoshimi Sueishi 2003
[b-Cyclodextrin](1).[4-Cl-Phenol] 2.43 6.9 40.0 UV-vis spectroscopy Yoshimi Sueishi 2003
[b-Cyclodextrin](1).[1,2-propanediol] 0.00 -1.30 0.8 25.0 UV/VIS spectrometry Jorge Pérez-Juste 2006
[b-Cyclodextrin](1).[4-Br-Phenol] 2.48 6.9 40.0 UV-vis spectroscopy Yoshimi Sueishi 2003
[b-Cyclodextrin](1).[4-NO2-Phenol] 2.57 6.9 40.0 UV-vis spectroscopy Yoshimi Sueishi 2003
[b-Cyclodextrin](1).[4-C2H5-Phenol] 2.76 6.9 40.0 UV-vis spectroscopy Yoshimi Sueishi 2003
[b-Cyclodextrin](1).[4-CH3-Phenol] 2.80 6.9 40.0 UV-vis spectroscopy Yoshimi Sueishi 2003
[b-Cyclodextrin](1).[4-I-Phenol] 3.30 6.9 40.0 UV-vis spectroscopy Yoshimi Sueishi 2003
[b-Cyclodextrin](1).[4-(CH3)2CH-Phenol] 3.52 6.9 40.0 UV-vis spectroscopy Yoshimi Sueishi 2003
[b-Cyclodextrin](1).[1,2-butanediol] 0.56 -1.30 0.8 25.0 UV/VIS spectrometry Jorge Pérez-Juste 2006
[b-Cyclodextrin](2).[methyl orange] 4.76 2.60 7.0 25.0 UV-vis spectroscopy Yoshimi Sueishi 2004
[b-Cyclodextrin](2).[methyl orange] 5.32 3.48 25.0 UV-vis spectroscopy Yoshimi Sueishi 2004
[b-Cyclodextrin](1).[1,2-penatnediol] 1.06 -0.30 0.8 25.0 UV/VIS spectrometry Jorge Pérez-Juste 2006
[b-Cyclodextrin](1).[C8NBr] -2.97 7.0 25.0 titration microcalorimetry De-Zhi Sun 2004
[b-Cyclodextrin](1).[C12NBr] -1.54 7.0 25.0 titration microcalorimetry De-Zhi Sun 2004
[b-Cyclodextrin](2).[C14NBr] -0.85 7.0 25.0 titration microcalorimetry De-Zhi Sun 2004
[b-Cyclodextrin](1).[paeonol] 3.52 7.0 25.0 isothermal titration calorimetry De-Zhi Sun 2006
[b-Cyclodextrin](1).[acetovanillone] 2.97 7.0 25.0 isothermal titration calorimetry De-Zhi Sun 2006
[b-Cyclodextrin](1).[2-hydroxyl-5-methoxyacetophone] 2.82 7.0 25.0 isothermal titration calorimetry De-Zhi Sun 2006
[b-Cyclodextrin](2).[2-hydroxyl-5-methoxyacetophone] 6.61 7.0 25.0 isothermal titration calorimetry De-Zhi Sun 2006
[b-Cyclodextrin](1).[1,2-hexanediol] 1.52 0.30 0.8 25.0 UV/VIS spectrometry Jorge Pérez-Juste 2006
[b-Cyclodextrin](1).[1,3-propanediol] 0.24 -1.30 0.8 25.0 UV/VIS spectrometry Jorge Pérez-Juste 2006
[b-Cyclodextrin](1).[N,N'-Diheptyl-4,4'-bipyridinium] 2.53 1.56 8.0 25.0 UV-vis spectroscopy Iwao Suzuki 2006
[b-Cyclodextrin](2).[N,N'-Diheptyl-4,4'-bipyridinium] 2.73 1.76 8.0 25.0 UV-vis spectroscopy Iwao Suzuki 2006
[b-Cyclodextrin](1).[1,4-butanediol] 0.58 -1.30 0.8 25.0 UV/VIS spectrometry Jorge Pérez-Juste 2006
[b-Cyclodextrin](1).[gemfibrozil] 2.88 9.1 Fluorescence spectroscopy Bo Tang 2004
[b-Cyclodextrin](1).[ketoconazole] 3.97 2.30 6.0 25.0 UV-vis spectroscopy Joanna Taraszewska 2005
[b-Cyclodextrin](1).[1,5-penatnediol] 1.22 -0.30 0.8 25.0 UV/VIS spectrometry Jorge Pérez-Juste 2006
[b-Cyclodextrin](1).[tetrasulfonated 1,2-bis(diphenylphosphino)ethane] 3.18 2.18 7.0 25.0 NMR spectroscopy Sebastien Tilloy 2006
[b-Cyclodextrin](1).[tetrasulfonated 1,2-bis(diphenylphosphino)ethane] 2.91 1.90 7.0 25.0 UV-vis spectroscopy Sebastien Tilloy 2006
[b-Cyclodextrin](1).[tetrasulfonated 1,3-bis(diphenylphosphino)propane] 3.28 2.28 7.0 25.0 NMR spectroscopy Sebastien Tilloy 2006
[b-Cyclodextrin](1).[tetrasulfonated 1,3-bis(diphenylphosphino)propane] 2.97 1.95 7.0 25.0 UV-vis spectroscopy Sebastien Tilloy 2006
[b-Cyclodextrin](1).[tetrasulfonated 1,4-bis(diphenylphosphino)butane] 3.20 2.20 7.0 25.0 NMR spectroscopy Sebastien Tilloy 2006
[b-Cyclodextrin](1).[tetrasulfonated 1,4-bis(diphenylphosphino)butane] 2.93 1.93 7.0 25.0 UV-vis spectroscopy Sebastien Tilloy 2006
[b-Cyclodextrin](1).[naftifine] 2.71 1.52 12.0 25.0 UV-vis spectroscopy Itziar Velaz 2006
[b-Cyclodextrin](1).[5-(2,4-difluorophenylsalicylic) acid] 6.98 6.66 7.4 5.0 Ion selective electrode potentiometry P.E. Macheras 1999
[b-Cyclodextrin](1).[5-(2,4-difluorophenylsalicylic) acid] 6.63 6.09 7.4 15.0 Ion selective electrode potentiometry P.E. Macheras 1999
[b-Cyclodextrin](1).[5-(2,4-difluorophenylsalicylic) acid] 4.89 3.58 7.4 25.0 Ion selective electrode potentiometry P.E. Macheras 1999
[b-Cyclodextrin](1).[5-(2,4-difluorophenylsalicylic) acid] 4.31 3.00 7.4 37.0 Ion selective electrode potentiometry P.E. Macheras 1999
[b-Cyclodextrin](1).[1,6-hexanediol] 1.70 0.30 0.8 25.0 UV/VIS spectrometry Jorge Pérez-Juste 2006
[b-Cyclodextrin](1).[decanesulfonate] 3.50 2.58 7.0 25.0 Reverse-phase liquid chromatography Robert E. Synovec 1999
[b-Cyclodextrin](1).[decanesulfonate] 3.68 3.10 7.0 25.0 Flow injection analysis with dynamic surface tension detection Robert E. Synovec 1999
[b-Cyclodextrin](1).[4-F-phenol] 2.02 5.8 20.0 UV-vis spectroscopy; spectral displacement method D. Landy 2000
[b-Cyclodextrin](1).[4-F-phenol] 2.03 0.85 5.8 20.0 UV-vis spectroscopy D. Landy 2000
[b-Cyclodextrin](1).[4-F-phenol] 2.02 1.40 7.0 20.0 NMR spectroscopy D. Landy 2000
[b-Cyclodextrin](1).[4-Cl-phenol] 2.43 5.8 20.0 UV-vis spectroscopy; spectral displacement method D. Landy 2000
[b-Cyclodextrin](1).[4-Br-phenol] 2.63 5.8 20.0 UV-vis spectroscopy; spectral displacement method D. Landy 2000
[b-Cyclodextrin](1).[4-I-phenol] 2.96 5.8 20.0 UV-vis spectroscopy; spectral displacement method D. Landy 2000
[b-Cyclodextrin](1).[4-methylphenol] 2.29 5.8 20.0 UV-vis spectroscopy; spectral displacement method D. Landy 2000
[b-Cyclodextrin](1).[4-CN-phenol] 2.30 5.8 20.0 UV-vis spectroscopy; spectral displacement method D. Landy 2000
[b-Cyclodextrin](1).[4-CN-phenol] 2.29 0.90 5.8 20.0 UV-vis spectroscopy D. Landy 2000
[b-Cyclodextrin](1).[4-CN-phenol] 2.26 1.48 7.0 20.0 NMR spectroscopy D. Landy 2000
[b-Cyclodextrin](1).[dodecane 1,12-bis(trimethylammonium bromide)] 3.48 2.62 6.0 25.0 NMR spectroscopy Celia Cabaleiro-Lago 2006
[b-Cyclodextrin](1).[dodecane 1,12-bis(trimethylammonium bromide)] 3.40 2.00 6.0 25.0 Electrical conductivity measurements Celia Cabaleiro-Lago 2006
[b-Cyclodextrin](1).[4-OH-phenol] 2.06 5.8 20.0 UV-vis spectroscopy; spectral displacement method D. Landy 2000
[b-Cyclodextrin](1).[4-OH-phenol] 2.06 0.78 5.8 20.0 UV-vis spectroscopy D. Landy 2000
[b-Cyclodextrin](1).[4-OH-phenol] 2.00 1.00 7.0 20.0 NMR spectroscopy D. Landy 2000
[b-Cyclodextrin](1).[4-OCH3-phenol] 2.23 5.8 20.0 UV-vis spectroscopy; spectral displacement method D. Landy 2000
[b-Cyclodextrin](1).[4-OC2H5-phenol] 2.52 5.8 20.0 UV-vis spectroscopy; spectral displacement method D. Landy 2000
[b-Cyclodextrin](1).[4-OC3H7-phenol] 2.74 5.8 20.0 UV-vis spectroscopy; spectral displacement method D. Landy 2000
[b-Cyclodextrin](1).[4-CHO-phenol] 2.30 5.8 20.0 UV-vis spectroscopy; spectral displacement method D. Landy 2000
[b-Cyclodextrin](1).[4-CH2OH-phenol] 2.04 5.8 20.0 UV-vis spectroscopy; spectral displacement method D. Landy 2000
[b-Cyclodextrin](1).[4-CH2COOH-phenol] 1.98 5.8 20.0 UV-vis spectroscopy; spectral displacement method D. Landy 2000
[b-Cyclodextrin](1).[4-SO3H-phenol] 1.85 5.8 20.0 UV-vis spectroscopy; spectral displacement method D. Landy 2000
[b-Cyclodextrin](1).[polymyxin B] 3.48 6.0 25.0 Surface tension measurements Adam Baszkin 1999
[b-Cyclodextrin](1).[piroxicam] 1.94 4.5 25.0 UV-vis spectroscopy A.G. Oliveira 1999
[b-Cyclodextrin](1).[piroxicam] 1.79 5.0 25.0 UV-vis spectroscopy A.G. Oliveira 1999
[b-Cyclodextrin](1).[piroxicam] 1.48 5.5 25.0 UV-vis spectroscopy A.G. Oliveira 1999
[b-Cyclodextrin](1).[piroxicam] 1.46 6.0 25.0 UV-vis spectroscopy A.G. Oliveira 1999
[b-Cyclodextrin](1).[sulfaproxyline] 2.97 2.08 7.0 25.0 UV-vis spectroscopy Barbara Szafran 1999
[b-Cyclodextrin](1).[2,3-diazabicyclo[2.2.2]oct-2-ene] 3.04 2.48 7.0 25.0 NMR spectroscopy Werner M. Nau 1999
[b-Cyclodextrin](1).[2,3-diazabicyclo[2.2.2]oct-2-ene] 2.95 2.00 7.0 25.0 UV-vis spectroscopy Werner M. Nau 1999
[b-Cyclodextrin](1).[[(h5-C5H5)Fe(h5-C5H4CH2N(CH3)2CH2(p-C6H4)CH2N(CH3)2CH2h5-C5H4)Fe(h5-C5H5)]2+] 3.57 2.60 7.0 25.0 Fluorescence spectroscopy Donal H. Macartney 1999
[b-Cyclodextrin](2).[[(h5-C5H5)Fe(h5-C5H4CH2N(CH3)2CH2(p-C6H4)CH2N(CH3)2CH2h5-C5H4)Fe(h5-C5H5)]2+] 3.18 2.30 7.0 25.0 Fluorescence spectroscopy Donal H. Macartney 1999
[b-Cyclodextrin](1).[[(h5-C5H5)Fe(h5-C5H4CH2N(CH3)2(CH2)12N-(CH3)2CH2h5-C5H4)Fe(h5-C5H5)]2+] 3.83 2.90 7.0 25.0 Fluorescence spectroscopy Donal H. Macartney 1999
[b-Cyclodextrin](2).[[(h5-C5H5)Fe(h5-C5H4CH2N(CH3)2(CH2)12N-(CH3)2CH2h5-C5H4)Fe(h5-C5H5)]2+] 3.20 2.30 7.0 25.0 Fluorescence spectroscopy Donal H. Macartney 1999
[b-Cyclodextrin](1).[[(h5-C5H5)Fe(h5-C5H4CH2N(CH3)2CH2h5-C5H4)Fe(h5-C5H5)]+] 3.60 2.70 7.0 25.0 Fluorescence spectroscopy Donal H. Macartney 1999
[b-Cyclodextrin](2).[[(h5-C5H5)Fe(h5-C5H4CH2N(CH3)2CH2h5-C5H4)Fe(h5-C5H5)]+] 3.18 2.30 7.0 25.0 Fluorescence spectroscopy Donal H. Macartney 1999
[b-Cyclodextrin](1).[mordant orange 1] 2.78 7.2 25.0 Circular dichroism spectroscopy Yoshihisa Inoue 1999
[b-Cyclodextrin](1).[sodium 2-(p-toluidinyl)naphthalene-6-sulfonate] 3.56 7.2 25.0 Fluorescence spectroscopy Yoshihisa Inoue 1999
[b-Cyclodextrin](1).[Tb-podate] 6.02 7.3 20.0 Luminescence titrations Jean-Claude G. Bünzli 2000
[b-Cyclodextrin](1).[2,4-dichlorophenoxyacetic acid] 2.53 7.0 25.0 UV-vis spectroscopy J. I. Perez-Martinez 2000
[b-Cyclodextrin](1).[2,4-dichlorophenoxyacetic acid] 2.53 25.0 X-ray diffraction, differential scanning calorimetry, infrared spectroscopy, scanning electron microscopy Pedro J. Sanchez-Soto 1996
[b-Cyclodextrin](1).[gliclazide] 2.29 7.0 25.0 UV-vis spectroscopy Hassan Y. Aboul-Enein 2000
[b-Cyclodextrin](4).[p-Tert-butylbenzyl-functionalized p-pyridylporphyrins] 4.54 7.0 25.0 Microcalorimetry Jurriaan Huskens 2001
[b-Cyclodextrin](4).[p-Tert-butylbenzyl-functionalized m-pyridylporphyrins] 4.40 7.0 25.0 Microcalorimetry Jurriaan Huskens 2001
[b-Cyclodextrin](1).[ammonium 8-anilino-1-naphthalenesulfonic acid] 2.05 7.0 25.0 Fluorescence spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[sodium 6-(p-toludino)-2-naphthalenesulfonate] 3.56 7.0 25.0 Fluorescence spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[3-chlorophenol] 2.30 1.67 2.0 20.0 UV-vis spectroscopy Miguel A. Garcia-Garibay 2001
[b-Cyclodextrin](1).[3-chlorophenol] 2.48 1.08 7.0 20.0 NMR spectroscopy Miguel A. Garcia-Garibay 2001
[b-Cyclodextrin](1).[2-chlorophenol] 2.04 1.18 2.0 20.0 UV-vis spectroscopy Miguel A. Garcia-Garibay 2001
[b-Cyclodextrin](1).[2-chlorophenol] 2.18 0.95 7.0 20.0 NMR spectroscopy Miguel A. Garcia-Garibay 2001
[b-Cyclodextrin](1).[3,4-dichlorophenol] 3.00 1.78 4.5 20.0 UV-vis spectroscopy Miguel A. Garcia-Garibay 2001
[b-Cyclodextrin](1).[3,4-dichlorophenol] 3.32 1.45 7.0 20.0 NMR spectroscopy Miguel A. Garcia-Garibay 2001
[b-Cyclodextrin](1).[2,4-dichlorophenol] 2.54 1.36 4.5 20.0 UV-vis spectroscopy Miguel A. Garcia-Garibay 2001
[b-Cyclodextrin](1).[2,4-dichlorophenol] 2.75 1.23 7.0 20.0 NMR spectroscopy Miguel A. Garcia-Garibay 2001
[b-Cyclodextrin](1).[2,6-dichlorophenol] 1.70 0.78 4.5 20.0 UV-vis spectroscopy Miguel A. Garcia-Garibay 2001
[b-Cyclodextrin](1).[4-amino-N-[5-methyl-1,3,4-thiadiazol-2-yl]-benzenesulphonamide] 2.81 7.0 37.0 UV-vis spectroscopy Juan J. Torres-Labandeira 2001
[b-Cyclodextrin](1).[4-amino-N-[5-methyl-1,3,4-thiadiazol-2-yl]-benzenesulphonamide] 2.81 37.0 UV spectroscopy Juan J. Torres-Labandeira 2001
[b-Cyclodextrin](1).[nimodipine] 2.74 1.51 7.0 25.0 UV-vis spectroscopy Frantisek Kopecky 2001
[b-Cyclodextrin](1).[phenacetin] 2.26 0.48 4.5 37.0 HPLC-method Kaneto Uekama 2001
[b-Cyclodextrin](1).[phenacetin] 2.26 7.4 37.0 HPLC-method J. Howard Rytting 2002
[b-Cyclodextrin](1).[m-bromobenzoic acid] 2.49 0.70 3.5 37.0 HPLC-method Kaneto Uekama 2001
[b-Cyclodextrin](1).[o-toluic acid] 2.04 0.48 4.5 37.0 HPLC-method Kaneto Uekama 2001
[b-Cyclodextrin](1).[Brilliant Green] 3.34 7.2 25.0 UV-vis spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[Auramine O] 2.91 7.2 25.0 UV-vis spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[Tropaeolin OO] 3.74 7.2 25.0 UV-vis spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[8-anilinonaphthalenesulfonate] 2.01 7.2 25.0 Fluorescence spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[benzoic acid] 2.90 1.43 25.0 Ágnes Buvári-Barcza 2002
[b-Cyclodextrin](1).[benzoic acid] 3.06 7.0 UV/VIS Spectroscopy Qing-Xhiang Guo 2001
[b-Cyclodextrin](1).[1,2-dithiolane-3-pentanoic acid] 3.22 9.0 20.0 Capillary electrophoresis Tommaso Carofiglio 2002
[b-Cyclodextrin](1).[benzene] 2.11 1.30 25.0 Ágnes Buvári-Barcza 2002
[b-Cyclodextrin](1).[benzene] 2.05 0.85 25.0 GC (SHSGC) É. Fenyvesi 2005
[b-Cyclodextrin](1).[acetic acid ] 1.30 0.30 25.0 Ágnes Buvári-Barcza 2002
[b-Cyclodextrin](1).[nicardipine] 1.31 -0.28 7.0 UV-vis spectroscopy Francisco J. B. Veiga 2002
[b-Cyclodextrin](1).[nicardipine] 1.18 -0.85 3.0 UV-vis spectroscopy Francisco J. B. Veiga 2002
[b-Cyclodextrin](1).[nicardipine] 1.51 -0.04 5.5 UV-vis spectroscopy Francisco J. B. Veiga 2002
[b-Cyclodextrin](1).[nicardipine] 1.88 0.78 7.4 UV-vis spectroscopy Francisco J. B. Veiga 2002
[b-Cyclodextrin](1).[cyclopentanol ] 2.24 0.70 Microcalorimetric titrations Yu Liu 2003
[b-Cyclodextrin](1).[cyclohexanecarboxylic acid] 2.42 Potentiometry Yu Liu 2003
[b-Cyclodextrin](1).[N-Cbz-L-alanine] 2.17 0.60 Microcalorimetric titrations Yu Liu 2003
[b-Cyclodextrin](1).[rimantidine] 4.55 3.08 7.0 30.0 Isothermal titration calorimetry (ITC) José Vázquez Tato 2005
[b-Cyclodextrin](1).[sodium 6-p-toluidino-2-naphthalenesulfonic acid] 3.56 7.2 25.0 UV-vis spectroscopy Yu Liu 2003
[b-Cyclodextrin](1).[sodium 6-p-toluidino-2-naphthalenesulfonic acid] 3.38 6.0 25.0 Fluorescence spectroscopy Yu Liu 2002
[b-Cyclodextrin](1).[4-nitrobenzenediazonium] 3.41 8.0 35.0 HPLC-method Carlos Bravo-Díaz 2003
[b-Cyclodextrin](1).[adamantyl-methanol] 5.15 3.70 7.0 30.0 Isothermal titration calorimetry (ITC) José Vázquez Tato 2005
[b-Cyclodextrin](1).[natamycin] 3.00 7.0 25.0 UV-vis spectroscopy Joseph E. Marcy 2003
[b-Cyclodextrin](1).[acyclovir] 1.34 7.0 25.0 UV-vis spectroscopy Helene Parrot-Lopez 2003
[b-Cyclodextrin](1).[vinpocetine] 1.85 7.0 22.0 UV-vis spectroscopy Laura Ribeiro 2002
[b-Cyclodextrin](1).[cycloheptanol ] 3.37 1.96 7.2 25.0 titration microcalorimetry Yu Liu 2004
[b-Cyclodextrin](1).[(+)-camphor] 3.92 2.42 7.2 25.0 titration microcalorimetry Yu Liu 2004
[b-Cyclodextrin](1).[(-)-camphor ] 3.70 1.78 7.2 25.0 titration microcalorimetry Yu Liu 2004
[b-Cyclodextrin](1).[(+)-borneol ] 4.27 2.04 7.2 25.0 titration microcalorimetry Yu Liu 2004
[b-Cyclodextrin](1).[(-)-borneol] 4.30 2.76 7.2 25.0 titration microcalorimetry Yu Liu 2004
[b-Cyclodextrin](1).[α-asarone] 3.11 7.2 25.0 Fluorescence spectroscopy Yu Liu 2003
[b-Cyclodextrin](1).[ferulic acid] 3.61 7.2 25.0 Fluorescence spectroscopy Yu Liu 2003
[b-Cyclodextrin](1).[magnolol] 3.71 7.2 25.0 Fluorescence spectroscopy Yu Liu 2003
[b-Cyclodextrin](1).[honokiol] 3.37 7.2 25.0 Fluorescence spectroscopy Yu Liu 2003
[b-Cyclodextrin](1).[deoxycholate] 3.69 1.20 7.2 25.0 Microcalorimetric titrations Yu Liu 2003
[b-Cyclodextrin](1).[cholate] 3.61 1.92 7.2 25.0 Microcalorimetric titrations Yu Liu 2003
[b-Cyclodextrin](1).[glycocholate] 3.38 1.84 7.2 25.0 Microcalorimetric titrations Yu Liu 2003
[b-Cyclodextrin](1).[taurocholate] 3.36 1.11 7.2 25.0 Microcalorimetric titrations Yu Liu 2003
[b-Cyclodextrin](1).[taurocholate] 2.49 7.4 37.0 HPLC-method J. Howard Rytting 2002
[b-Cyclodextrin](1).[norflurazon] 2.56 7.0 25.0 HPLC-method Jaime Villaverde 2004
[b-Cyclodextrin](1).[norflurazon] 2.56 HPLC Jaime Villaverde 2006
[b-Cyclodextrin](1).[L-phenylalanine] 5.65 5.00 7.0 25.0 UV-vis spectroscopy Margarita Valero 2003
[b-Cyclodextrin](1).[L-phenylalanine] 0.48 0.85 5.01 25.0 Titration calorimetry Robert N. Goldberg 1994
[b-Cyclodextrin](1).[L-phenylalanine] 4.26 7.0 25.0 microcalorimetry Giuseppina Castronuovo 1995
[b-Cyclodextrin](1).[L-phenylalanine] 5.03 11.3 25.0 microcalorimetry Giuseppina Castronuovo 1995
[b-Cyclodextrin](1).[L-phenylalanine] 1.70 0.73 9.88 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[L-phenylalanine] 1.34 1.00 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[b-Cyclodextrin](1).[flourescein] 1.07 6.0 25.0 Fluorescence spectroscopy Yu Liu 2002
[b-Cyclodextrin](1).[benzoate] 1.68 0.30 7.0 25.0 Affinity capillary electrophoresis Oliver Steinbock 2001
[b-Cyclodextrin](1).[2-hydroxybenzoate] 2.48 1.58 7.0 25.0 Affinity capillary electrophoresis Oliver Steinbock 2001
[b-Cyclodextrin](1).[amantadine] 3.95 7.0 25.0 Isothermal microcalorimetry titration Gaio Paradossi 2006
[b-Cyclodextrin](1).[3-hydroxybenzoate] 1.57 7.0 25.0 Affinity capillary electrophoresis Oliver Steinbock 2001
[b-Cyclodextrin](1).[4-hydroxybenzoate] 2.36 0.95 7.0 25.0 Affinity capillary electrophoresis Oliver Steinbock 2001
[b-Cyclodextrin](1).[2,4-dihydroxybenzoate] 2.95 2.04 7.0 25.0 Affinity capillary electrophoresis Oliver Steinbock 2001
[b-Cyclodextrin](1).[2,3-diazabicyclo[2,2,2]oct-2-ene] 3.04 2.30 7.0 25.0 UV-vis spectroscopy and NMR spetroscopy Werner M. Nau 2002
[b-Cyclodextrin](1).[4-methyl-1-isopropyl-2,3-diazabicyclo[2.2.2]oct-2-ene] 2.95 2.18 7.0 25.0 UV-vis spectroscopy and NMR spetroscopy Werner M. Nau 2002
[b-Cyclodextrin](1).[1,4-dichloro-2,3-diazabicyclo[2.2.2]oct-2-ene] 3.28 2.48 7.0 25.0 UV-vis spectroscopy and NMR spetroscopy Werner M. Nau 2002
[b-Cyclodextrin](1).[1-hydroxymethyl-2,3-diazabicyclo[2.2.2]oct-2-ene] 2.26 1.30 7.0 25.0 UV-vis spectroscopy and NMR spetroscopy Werner M. Nau 2002
[b-Cyclodextrin](1).[1-aminomethyl-2,3-diazabicyclo[2.2.2]oct-2-ene ] 2.40 1.30 11.0 25.0 UV-vis spectroscopy and NMR spetroscopy Werner M. Nau 2002
[b-Cyclodextrin](1).[1-aminomethyl-2,3-diazabicyclo[2.2.2]oct-2-ene ] 1.30 1.00 5.0 25.0 Induced circular dichroism Werner M. Nau 2002
[b-Cyclodextrin](1).[nitrobenzene] 2.11 5.0 25.0 Differential pulse polarography Carlos Bravo-Diaz 2002
[b-Cyclodextrin](1).[nitrobenzene] 2.45 1.08 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[nitrobenzene] 1.70 0.48 Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[diclofenac sodium] 3.22 1.00 7.0 37.0 Calorimetry R. Chadha 2002
[b-Cyclodextrin](1).[p-nitrobenzenediazonium] 3.36 5.0 25.0 Differential pulse polarography Carlos Bravo-Diaz 2002
[b-Cyclodextrin](1).[p-nitrobenzenediazonium] 3.42 5.0 25.0 UV-vis spectroscopy Carlos Bravo-Diaz 2002
[b-Cyclodextrin](1).[3-formyl-phenoxathiin] 3.71 Fluorescence spectroscopy Mihaela Hillebrand 2002
[b-Cyclodextrin](1).[3-acetyl-phenoxathiin] 3.89 Fluorescence spectroscopy Mihaela Hillebrand 2002
[b-Cyclodextrin](1).[3-carboxyphenoxathiin] 3.18 2.11 Fluorescence spectroscopy Mihaela Hillebrand 2002
[b-Cyclodextrin](1).[3-carboxyphenoxathiin] 3.87 9.18 Fluorescence spectroscopy Mihaela Hillebrand 2002
[b-Cyclodextrin](1).[3-carboxyphenoxathiin] 3.75 9.8 25.0 NMR spectroscopy Andre Thevand 2003
[b-Cyclodextrin](1).[1-Adamantylmethyl α-D-Glucopyranoside] 5.14 4.96 7.0 25.0 NMR spectroscopy Soledad Penadés 2004
[b-Cyclodextrin](1).[1-Adamantylmethyl α-D-Glucopyranoside] 5.14 4.36 7.0 30.0 NMR spectroscopy Soledad Penadés 2004
[b-Cyclodextrin](1).[1-Adamantylmethyl α-D-Glucopyranoside] 5.01 4.32 7.0 40.0 NMR spectroscopy Soledad Penadés 2004
[b-Cyclodextrin](1).[2,4,6-trichlorophenol] 2.01 3.0 24.0 UV-vis spectroscopy K. Hanna 2003
[b-Cyclodextrin](1).[2,4,6-trichlorophenol] 0.95 8.8 24.0 UV-vis spectroscopy K. Hanna 2003
[b-Cyclodextrin](1).[cinchonidine] 2.03 7.2 25.0 Fluorescence spectroscopy Yu Liu 2003
[b-Cyclodextrin](1).[cinchonine] 2.07 7.2 25.0 Fluorescence spectroscopy Yu Liu 2003
[b-Cyclodextrin](1).[p-Methyl red-modified b-CD] 1.63 1.0 25.0 Induced circular dichroism Tetsuo Kuwabara 2002
[b-Cyclodextrin](1).[phenolphthaleinmodified-b-CD] 2.90 10.8 25.0 Induced circular dichroism Tetsuo Kuwabara 2002
[b-Cyclodextrin](1).[1-Adamantylmethyl β-D-Glucopyranoside] 5.64 4.56 7.0 25.0 NMR spectroscopy Soledad Penadés 2004
[b-Cyclodextrin](1).[1-Adamantylmethyl β-D-Glucopyranoside] 5.65 4.54 7.0 30.0 NMR spectroscopy Soledad Penadés 2004
[b-Cyclodextrin](1).[1-Adamantylmethyl β-D-Glucopyranoside] 5.72 4.77 7.0 40.0 NMR spectroscopy Soledad Penadés 2004
[b-Cyclodextrin](1).[R-5-methoxy-3-(di-n-propylamino)chroman] 1.76 7.0 25.0 Capillary electrophoresis Ph. Morin 1995
[b-Cyclodextrin](1).[S-5-methoxy-3-(di-n-propylamino)chroman] 1.86 7.0 25.0 Capillary electrophoresis Ph. Morin 1995
[b-Cyclodextrin](1).[R-5-hydroxy-3-(di-n-propylamino)chroman] 2.14 7.0 25.0 Capillary electrophoresis Ph. Morin 1995
[b-Cyclodextrin](1).[S-5-hydroxy-3-(di-n-propylamino)chroman] 2.22 7.0 25.0 Capillary electrophoresis Ph. Morin 1995
[b-Cyclodextrin](1).[cis-phenylalanylproline] 1.98 7.3 27.0 NMR spectroscopy Cynthia K. Larive 1995
[b-Cyclodextrin](1).[phenolphthalein ] 4.38 3.30 10.5 23.5 Gradient flow injection spectrophotometric technique Michael A. Koupparis 1995
[b-Cyclodextrin](1).[2-(cyclohexylamino)ethanesulfonic acid] 2.69 1.30 10.2 27.0 Gradient flow injection spectrophotometric technique Michael A. Koupparis 1995
[b-Cyclodextrin](1).[1-(hydroxymethyl)adamantane] 5.45 4.59 7.0 25.0 NMR spectroscopy Soledad Penadés 2004
[b-Cyclodextrin](1).[3-(cyclohexylamino)propanesulfonic acid ] 2.68 1.70 11.5 25.0 Gradient flow injection spectrophotometric technique Michael A. Koupparis 1995
[b-Cyclodextrin](1).[salbutamol] 0.98 7.0 37.0 Affinity capillary electrophoresis M. Taverna 1996
[b-Cyclodextrin](1).[atrazine] 3.29 7.0 Polarography L. Pospisil 1998
[b-Cyclodextrin](1).[diclofenac] 3.10 0.40 3.5 20.0 Potentiometry Graciela M. Escandar 1999
[b-Cyclodextrin](1).[diclofenac] 3.00 0.10 3.5 20.0 Spetrophotometry Graciela M. Escandar 1999
[b-Cyclodextrin](1).[diclofenac] 3.11 0.03 3.5 20.0 Spectrofluorimetry Graciela M. Escandar 1999
[b-Cyclodextrin](1).[diclofenac] 3.00 0.40 7.0 20.0 Potentiometry Graciela M. Escandar 1999
[b-Cyclodextrin](1).[diclofenac] 3.15 0.05 7.0 20.0 Spectrofluorimetry Graciela M. Escandar 1999
[b-Cyclodextrin](1).[diclofenac] 2.47 7.0 25.0 UV-vis spectroscopy Maria Immacolata La Rotonda 2004
[b-Cyclodextrin](1).[diclofenac] 2.55 7.0 25.0 Circular dichroism spectroscopy Maria Immacolata La Rotonda 2004
[b-Cyclodextrin](1).[Naphtalene-1-sulfonate] 1.49 0.69 3.0 25.0 Capillary electrophoresis Wang-Hsien Ding 2004
[b-Cyclodextrin](1).[Naphtalene-1-sulfonate] 1.48 9.2 25.0 Capillary electrophoresis Wang-Hsien Ding 2004
[b-Cyclodextrin](1).[L-Tryptophan] 1.80 7.2 25.0 Fluorometric titrations Yu Liu 2001
[b-Cyclodextrin](1).[D-Tryptophan] 1.40 7.2 25.0 Fluorometric titrations Yu Liu 2001
[b-Cyclodextrin](1).[L-Phenylalanine] 1.41 7.6 27.0 NMR spectroscopy Pornthep Sompornpisut 2002
[b-Cyclodextrin](1).[Poly(isobutene-alt-maleic acid)s modified with p-tert-butylphenyl groups] 4.45 3.00 7.5 25.0 Affinity capillary electrophoresis Bart Jan Ravoo 2002
[b-Cyclodextrin](1).[Poly(isobutene-alt-maleic acid)s modified with adamantyl groups] 3.30 2.48 7.5 25.0 Affinity capillary electrophoresis Bart Jan Ravoo 2002
[b-Cyclodextrin](1).[p-tert-butylbenzoate] 4.10 2.48 7.5 25.0 Affinity capillary electrophoresis Bart Jan Ravoo 2002
[b-Cyclodextrin](1).[2-carboxyphenoxathiin] 4.40 9.8 25.0 NMR spectroscopy Andre Thevand 2003
[b-Cyclodextrin](1).[Aflatoxin B1] 2.60 1.81 7.0 Fluorescence spectroscopy Rosangela Marchelli 2003
[b-Cyclodextrin](1).[Aflatoxin G1] 2.38 1.59 7.0 Fluorescence spectroscopy Rosangela Marchelli 2003
[b-Cyclodextrin](1).[Naphtalene-2-sulfonate] 2.58 1.33 3.0 25.0 Capillary electrophoresis Wang-Hsien Ding 2004
[b-Cyclodextrin](1).[Naphtalene-2-sulfonate] 2.51 9.2 25.0 Capillary electrophoresis Wang-Hsien Ding 2004
[b-Cyclodextrin](1).[Aflatoxin M3] 2.73 1.91 7.0 Fluorescence spectroscopy Rosangela Marchelli 2003
[b-Cyclodextrin](1).[Aflatoxin B2] 2.44 1.66 7.0 Fluorescence spectroscopy Rosangela Marchelli 2003
[b-Cyclodextrin](1).[Aflatoxin G2] 2.54 1.76 7.0 Fluorescence spectroscopy Rosangela Marchelli 2003
[b-Cyclodextrin](1).[4-(1-imidazolyl)phenol] 3.16 1.88 25.0 Electrospray Mass Spectrometry Yannis L. Loukas 2003
[b-Cyclodextrin](1).[3-hydroxy-benzylhydrazine] 3.04 1.76 25.0 Electrospray Mass Spectrometry Yannis L. Loukas 2003
[b-Cyclodextrin](1).[2-furoic hydrazide] 2.96 1.63 25.0 Electrospray Mass Spectrometry Yannis L. Loukas 2003
[b-Cyclodextrin](1).[2-amino-5,6-dimethyl-benzimidazole] 3.32 1.89 7.0 25.0 Fluorescence spectroscopy Ibrahim M. El-Mehasseb 2004
[b-Cyclodextrin](1).[Naphtalene-1,5-disulfonate] 0.92 0.18 3.0 25.0 Capillary electrophoresis Wang-Hsien Ding 2004
[b-Cyclodextrin](1).[Naphtalene-1,5-disulfonate] 0.91 9.2 25.0 Capillary electrophoresis Wang-Hsien Ding 2004
[b-Cyclodextrin](1).[tamoxifen] 4.18 7.4 37.0 High-performance affinity chromatography David S. Hage 2004
[b-Cyclodextrin](1).[phenytoin] 2.88 7.4 37.0 High-performance affinity chromatography David S. Hage 2004
[b-Cyclodextrin](1).[3,3',4',5',7-pentahydroxy flavone] 2.60 7.0 25.0 UV-vis spectroscopy Tayade Pralhad 2004
[b-Cyclodextrin](1).[dansyl-branched saccharide cyclophane] 2.89 7.0 25.0 Fluorescence spectroscopy Osamu Hayashida 2002
[b-Cyclodextrin](1).[Naphtalene-1,6-disulfonate] 1.86 1.12 3.0 25.0 Capillary electrophoresis Wang-Hsien Ding 2004
[b-Cyclodextrin](1).[Naphtalene-1,6-disulfonate] 1.82 9.2 25.0 Capillary electrophoresis Wang-Hsien Ding 2004
[b-Cyclodextrin](2).[b-ionone] 6.30 7.0 NMR spectroscopy N.E. Polyakov 2004
[b-Cyclodextrin](1).[b-caroten-8'-oic acid] 3.19 1.88 NMR spectroscopy Nikolai E. Polyakov 2004
[b-Cyclodextrin](1).[(−)-trans-4R-(4'-fluorophenyl)-3S-((3',4'-methylenedioxyphenoxy)methyl)piperidine] 3.42 2.70 7.0 20.0 NMR spectroscopy Andrea Bernini 2004
[b-Cyclodextrin](1).[(−)-trans-4R-(4'-fluorophenyl)-3S-((3',4'-methylenedioxyphenoxy)methyl)piperidine] 3.31 2.66 7.0 27.0 NMR spectroscopy Andrea Bernini 2004
[b-Cyclodextrin](1).[4[4-(methylsulfonyl) phenyl]-3-phenyl-2 (5H)-furazone] 1.79 7.2 25.0 UV-vis spectroscopy Tayade Pralhad 2004
[b-Cyclodextrin](1).[N-carboxybenzoyl-L-glutamic acid] 1.92 0.30 6.9 25.0 Isothermal titration calorimetry Yoshihisa Inoue 2004
[b-Cyclodextrin](1).[Naphtalene-2,6-disulfonate] 2.50 1.49 3.0 25.0 Capillary electrophoresis Wang-Hsien Ding 2004
[b-Cyclodextrin](1).[Naphtalene-2,6-disulfonate] 2.47 9.2 25.0 Capillary electrophoresis Wang-Hsien Ding 2004
[b-Cyclodextrin](1).[N-carboxybenzoyl-D-glutamic acid] 1.93 0.30 6.9 25.0 Isothermal titration calorimetry Yoshihisa Inoue 2004
[b-Cyclodextrin](1).[N-carboxybenzoyl-D-glutamyl-L-tyrosine] 2.06 0.48 6.9 25.0 Isothermal titration calorimetry Yoshihisa Inoue 2004
[b-Cyclodextrin](1).[N-carboxybenzoyl-L-glutamyl-L-tyrosine] 1.99 0.30 6.9 25.0 Isothermal titration calorimetry Yoshihisa Inoue 2004
[b-Cyclodextrin](1).[2,4,7-triamino-6-phenylpteridine] 2.22 7.0 25.0 UV-vis spectroscopy MS Nagarsenker 2004
[b-Cyclodextrin](1).[sodium cholate] 3.58 7.4 25.0 Isothermal titration calorimetry Yu Liu 2005
[b-Cyclodextrin](1).[sodium deoxycholate] 3.68 7.4 25.0 Isothermal titration calorimetry Yu Liu 2005
[b-Cyclodextrin](1).[sodium glycocholate] 3.41 7.4 25.0 Isothermal titration calorimetry Yu Liu 2005
[b-Cyclodextrin](1).[sodium taurocholate] 3.36 7.4 25.0 Isothermal titration calorimetry Yu Liu 2005
[b-Cyclodextrin](1).[3-aminonaphtalene-2,7-disulfonate] 2.66 1.86 3.0 25.0 Capillary electrophoresis Wang-Hsien Ding 2004
[b-Cyclodextrin](1).[3-aminonaphtalene-2,7-disulfonate] 2.64 9.2 25.0 Capillary electrophoresis Wang-Hsien Ding 2004
[b-Cyclodextrin](2).[gossypol] 3.65 7.0 25.0 UV-vis spectroscopy Xue-yi Ma 2005
[b-Cyclodextrin](1).[3,3 ,4 ,5,7-pentahydroxyflavone-3-rutinoside] 2.15 1.30 7.0 25.0 UV-vis spectroscopy S. Tommasini 2005
[b-Cyclodextrin](1).[3,3 ,4 ,5,7-pentahydroxyflavone-3-rutinoside] 2.18 1.30 7.0 25.0 Circular dichroism spectroscopy S. Tommasini 2005
[b-Cyclodextrin](1).[5,10,15-tris(3,5-dicarboxylatophenyl)-20-phenylporphyrin] 3.08 2.00 7.0 25.0 Isothermal titration calorimetry Koji Kano 2005
[b-Cyclodextrin](1).[Safranine T] 2.20 7.2 20.0 Fluorescence spectroscopy Shaomin Shuang 2005
[b-Cyclodextrin](1).[3-(a-acetonylbenzyl)-4-hydroxycoumarin] 2.80 1.2 37.0 UV-vis spectroscopy G. Zingone 2005
[b-Cyclodextrin](1).[3-(a-acetonylbenzyl)-4-hydroxycoumarin] 2.49 5.0 37.0 UV-vis spectroscopy G. Zingone 2005
[b-Cyclodextrin](1).[3-(a-acetonylbenzyl)-4-hydroxycoumarin] 2.47 5.5 37.0 UV-vis spectroscopy G. Zingone 2005
[b-Cyclodextrin](1).[3-(a-acetonylbenzyl)-4-hydroxycoumarin] 2.00 7.4 37.0 UV-vis spectroscopy G. Zingone 2005
[b-Cyclodextrin](1).[2-aminonaphtalene-1,5-disulfonate] 1.13 0.41 3.0 25.0 Capillary electrophoresis Wang-Hsien Ding 2004
[b-Cyclodextrin](1).[2-aminonaphtalene-1,5-disulfonate] 0.88 9.2 25.0 Capillary electrophoresis Wang-Hsien Ding 2004
[b-Cyclodextrin](1).[1-naphthol-4-sulfonate] 2.03 0.30 7.0 25.0 Fluorescence spectroscopy Shar S. Al-Shihry 2005
[b-Cyclodextrin](1).[Pentanoic acid] 1.49 0.85 11.3 25.0 Calorimetry Giuseppina Castronuovo 2005
[b-Cyclodextrin](1).[Nonanoic acid ] 2.41 1.78 11.3 25.0 Calorimetry Giuseppina Castronuovo 2005
[b-Cyclodextrin](1).[Decanoic acid ] 3.28 2.00 11.3 25.0 Calorimetry Giuseppina Castronuovo 2005
[b-Cyclodextrin](1).[Undecanoic acid ] 2.70 2.00 11.3 25.0 Calorimetry Giuseppina Castronuovo 2005
[b-Cyclodextrin](1).[Dodecanoic acid] 3.38 2.70 11.3 25.0 Calorimetry Giuseppina Castronuovo 2005
[b-Cyclodextrin](1).[triclosan] 2.88 7.0 25.0 UV-vis spectroscopy P. Mura 2005
[b-Cyclodextrin](1).[2-dibenzofuranol] 0.56 -1.30 7.0 15.0 Fluorescence spectroscopy Gustavo Gonzalez-Gaitano 2005
[b-Cyclodextrin](1).[2-dibenzofuranol] 0.47 -1.40 7.0 25.0 Fluorescence spectroscopy Gustavo Gonzalez-Gaitano 2005
[b-Cyclodextrin](1).[2-dibenzofuranol] 0.34 -1.52 7.0 35.0 Fluorescence spectroscopy Gustavo Gonzalez-Gaitano 2005
[b-Cyclodextrin](1).[2-dibenzofuranol] 0.22 -1.70 7.0 45.0 Fluorescence spectroscopy Gustavo Gonzalez-Gaitano 2005
[b-Cyclodextrin](1).[[(−)-(5R,6S)-7,8-didehydro-4,5-epoxy-3-methoxy-17-methyl-morphinan-6-ol]] 2.74 0.08 7.0 25.0 Potentiometry Lajos Barcza 2006
[b-Cyclodextrin](1).[phenolate] 2.27 23.0 NIR spectroscopy Chieu D. Tran 1995
[b-Cyclodextrin](1).[4-chlorophenolate] 2.35 23.0 NIR spectroscopy Chieu D. Tran 1995
[b-Cyclodextrin](1).[sodium-2-naphthalenesulfonate] 2.31 23.0 NIR spectroscopy Chieu D. Tran 1995
[b-Cyclodextrin](1).[cis-1-acetyl-4-[4-[2-(2,4-dichlorophenyl)-2(1H-imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]-piperazine] 2.92 5.0 25.0 UV spectroscopy J.J. Torres-Labandeira 1996
[b-Cyclodextrin](1).[cis-1-acetyl-4-[4-[2-(2,4-dichlorophenyl)-2(1H-imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]-piperazine] 2.88 5.0 30.0 UV spectroscopy J.J. Torres-Labandeira 1996
[b-Cyclodextrin](1).[cis-1-acetyl-4-[4-[2-(2,4-dichlorophenyl)-2(1H-imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]-piperazine] 3.02 5.0 37.0 UV spectroscopy J.J. Torres-Labandeira 1996
[b-Cyclodextrin](1).[cis-1-acetyl-4-[4-[2-(2,4-dichlorophenyl)-2(1H-imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]-piperazine] 3.10 6.0 25.0 UV spectroscopy J.J. Torres-Labandeira 1996
[b-Cyclodextrin](1).[cis-1-acetyl-4-[4-[2-(2,4-dichlorophenyl)-2(1H-imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]-piperazine] 3.95 6.0 30.0 UV spectroscopy J.J. Torres-Labandeira 1996
[b-Cyclodextrin](1).[cis-1-acetyl-4-[4-[2-(2,4-dichlorophenyl)-2(1H-imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]-piperazine] 3.84 6.0 37.0 UV spectroscopy J.J. Torres-Labandeira 1996
[b-Cyclodextrin](1).[trans-[[[4'-[(4-ethylphenyl)azo]phenyl]oxy]ethyl]trimethylammonuim bromide] 0.82 25.0 Induced circular dichroism Keishiro Shiahama 1996
[b-Cyclodextrin](1).[cis-[[[4'-[(4-ethylphenyl)azo]phenyl]oxy]ethyl]trimethylammonuim bromide] 0.49 25.0 Induced circular dichroism Keishiro Shiahama 1996
[b-Cyclodextrin](1).[trans-[[[4'-[(4-butylphenyl)azo]phenyl]oxy]ethyl]trimethylammonuim bromide] 1.40 25.0 Induced circular dichroism Keishiro Shiahama 1996
[b-Cyclodextrin](1).[trans-[[[4'-[(4-butylphenyl)azo]phenyl]oxy]ethyl]trimethylammonuim bromide] 1.26 25.0 Electromotive force potentiometric titration Keishiro Shiahama 1996
[b-Cyclodextrin](1).[3-nitrophenolate] 2.04 0.48 11.1 27.8 Capillary electrophoresis David M. Goodall 1995
[b-Cyclodextrin](1).[4-nitrophenolate] 3.18 2.22 11.1 27.8 Capillary electrophoresis David M. Goodall 1995
[b-Cyclodextrin](1).[Estradiol] 3.83 2.83 35.0 HPLC Nina Sadlej-Sosnowska 1997
[b-Cyclodextrin](1).[Ethinyloestradiol] 3.88 2.89 35.0 HPLC Nina Sadlej-Sosnowska 1997
[b-Cyclodextrin](1).[Estriol] 3.67 2.60 35.0 HPLC Nina Sadlej-Sosnowska 1997
[b-Cyclodextrin](1).[cis-[[[4'-[(4-butylphenyl)azo]phenyl]oxy]ethyl]trimethylammonuim bromide] 1.11 25.0 Induced circular dichroism Keishiro Shiahama 1996
[b-Cyclodextrin](1).[Estrone] 3.49 2.78 35.0 HPLC Nina Sadlej-Sosnowska 1997
[b-Cyclodextrin](1).[Nandrolone] 3.11 2.00 35.0 HPLC Nina Sadlej-Sosnowska 1997
[b-Cyclodextrin](1).[Norethisterone] 2.97 1.85 35.0 HPLC Nina Sadlej-Sosnowska 1997
[b-Cyclodextrin](1).[Methylprednisolone] 2.36 1.18 35.0 HPLC Nina Sadlej-Sosnowska 1997
[b-Cyclodextrin](1).[Methylprednisolone acetate] 2.36 1.30 35.0 HPLC Nina Sadlej-Sosnowska 1997
[b-Cyclodextrin](1).[Betamethasone phosphate] 2.54 1.85 35.0 HPLC Nina Sadlej-Sosnowska 1997
[b-Cyclodextrin](1).[Dexamethasone phosphate] 2.60 2.00 35.0 HPLC Nina Sadlej-Sosnowska 1997
[b-Cyclodextrin](1).[malic acid] 0.15 28.0 HPLC E. Fenyvesi 1999
[b-Cyclodextrin](1).[malic acid] 0.72 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[b-Cyclodextrin](1).[lactic acid ] 0.20 28.0 HPLC E. Fenyvesi 1999
[b-Cyclodextrin](1).[ascorbic acid] 0.57 28.0 HPLC E. Fenyvesi 1999
[b-Cyclodextrin](1).[tartaric acid] 0.61 28.0 HPLC E. Fenyvesi 1999
[b-Cyclodextrin](1).[tartaric acid] 0.89 0.36 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[b-Cyclodextrin](1).[citric acid] 1.11 28.0 HPLC E. Fenyvesi 1999
[b-Cyclodextrin](1).[citric acid] 1.70 1.59 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[b-Cyclodextrin](1).[BMS-191435(R)] 1.78 2.58 25.0 Chiral capillary electrophoresis Jinping Liu 1997
[b-Cyclodextrin](1).[BMS-191435(S)] 1.98 2.58 25.0 Chiral capillary electrophoresis Jinping Liu 1997
[b-Cyclodextrin](1).[4-nitro benzoic acid] 2.47 7.0 UV/VIS Spectroscopy Qing-Xhiang Guo 2001
[b-Cyclodextrin](1).[benzaldehyde] 2.17 7.0 UV/VIS Spectroscopy Qing-Xhiang Guo 2001
[b-Cyclodextrin](1).[4-nitro benzaldehyde] 2.02 7.0 UV/VIS Spectroscopy Qing-Xhiang Guo 2001
[b-Cyclodextrin](1).[4-nitro phenol] 2.46 7.0 UV/VIS Spectroscopy Qing-Xhiang Guo 2001
[b-Cyclodextrin](1).[aniline] 1.88 7.0 UV/VIS Spectroscopy Qing-Xhiang Guo 2001
[b-Cyclodextrin](1).[aniline] 1.79 fluorescence spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[4-nitro aniline] 2.49 7.0 UV/VIS Spectroscopy Qing-Xhiang Guo 2001
[b-Cyclodextrin](1).[6-thiopurine] 2.40 1.48 25.0 UV/VIS Spectroscopy Joel B. Alderete 2003
[b-Cyclodextrin](1).[Cd2+] 10.40 0.10 20.0 Polarography Eugenijus Norkus 2003
[b-Cyclodextrin](1).[methyl tert-butyl ether] 2.56 25.0 GC Ji-Won Yang 2003
[b-Cyclodextrin](1).[endo-8-azibicyclo[3.2.1]octan-3-ol] 4.05 3.48 NMR Udo H. Brinker 2004
[b-Cyclodextrin](1).[endo-8-azibicyclo[3.2.1]octan-3-ol] 4.03 3.30 Induced circular dichroism spectroscopy Udo H. Brinker 2004
[b-Cyclodextrin](1).[n-hexane] 0.99 0.48 25.0 GC (SHSGC) É. Fenyvesi 2005
[b-Cyclodextrin](1.7).[praziquantel] 2.60 30.0 UV spectroscopy Gordon Becket 1999
[b-Cyclodextrin](1).[n-heptane] 1.71 1.18 25.0 GC (SHSGC) É. Fenyvesi 2005
[b-Cyclodextrin](1).[n-octane] 1.68 0.70 25.0 GC (SHSGC) É. Fenyvesi 2005
[b-Cyclodextrin](1).[n-nonane] 1.86 0.78 25.0 GC (SHSGC) É. Fenyvesi 2005
[b-Cyclodextrin](1).[n-decane] 1.95 1.20 25.0 GC (SHSGC) É. Fenyvesi 2005
[b-Cyclodextrin](1).[n-undecane] 2.42 1.90 25.0 GC (SHSGC) É. Fenyvesi 2005
[b-Cyclodextrin](1).[n-dodecane] 2.38 1.76 25.0 GC (SHSGC) É. Fenyvesi 2005
[b-Cyclodextrin](1).[cyclohexane] 2.67 0.90 25.0 GC (SHSGC) É. Fenyvesi 2005
[b-Cyclodextrin](1).[Me-cyclohexane] 2.52 1.38 25.0 GC (SHSGC) É. Fenyvesi 2005
[b-Cyclodextrin](1).[Et-cyclohexane] 2.81 1.77 25.0 GC (SHSGC) É. Fenyvesi 2005
[b-Cyclodextrin](1).[o-xylene] 2.26 1.26 25.0 GC (SHSGC) É. Fenyvesi 2005
[b-Cyclodextrin](1).[m-xylene] 2.00 0.78 25.0 GC (SHSGC) É. Fenyvesi 2005
[b-Cyclodextrin](1).[p-xylene] 2.34 1.82 25.0 GC (SHSGC) É. Fenyvesi 2005
[b-Cyclodextrin](1).[Et-benzene] 2.46 2.24 25.0 GC (SHSGC) É. Fenyvesi 2005
[b-Cyclodextrin](1).[1,3,5-trimethyl-benzene] 1.62 1.08 25.0 GC (SHSGC) É. Fenyvesi 2005
[b-Cyclodextrin](1).[1,2,3-trimethyl-benzene] 2.37 1.46 25.0 GC (SHSGC) É. Fenyvesi 2005
[b-Cyclodextrin](1).[1,2,4-trimethyl-benzene] 2.37 1.43 25.0 GC (SHSGC) É. Fenyvesi 2005
[b-Cyclodextrin](1).[1-Nonanol] 3.69 2.00 25.0 GC Isao Sanemasa 1999
[b-Cyclodextrin](1).[decanoate ] 3.41 2.30 10.5 25.0 UV/VIS spectroscopy Bruno Szpoganicz 2001
[b-Cyclodextrin](1).[octanoate] 2.71 1.30 10.5 25.0 UV/VIS spectroscopy Bruno Szpoganicz 2001
[b-Cyclodextrin](1).[4-hydroxycoumarin derivative 1] 2.85 1.85 Fluorescence spectroscopy Suzanne Fery-Forgues 2001
[b-Cyclodextrin](1).[4-hydroxycoumarin derivative 2] 2.53 1.53 Fluorescence spectroscopy Suzanne Fery-Forgues 2001
[b-Cyclodextrin](1).[4-hydroxycoumarin derivative 3] 1.91 0.91 Fluorescence spectroscopy Suzanne Fery-Forgues 2001
[b-Cyclodextrin](1).[ADR(3)] 6.14 20.0 Fluorescence spectroscopy P. Ramamurthy 2001
[b-Cyclodextrin](1).[ADR(3)] 5.99 25.0 Fluorescence spectroscopy P. Ramamurthy 2001
[b-Cyclodextrin](1).[ADR(3)] 5.96 30.0 Fluorescence spectroscopy P. Ramamurthy 2001
[b-Cyclodextrin](1).[ADR(3)] 5.87 35.0 Fluorescence spectroscopy P. Ramamurthy 2001
[b-Cyclodextrin](1).[ADR(3)] 5.62 40.0 Fluorescence spectroscopy P. Ramamurthy 2001
[b-Cyclodextrin](1).[ADR(3)] 2.59 1.25 Fluorescence spectroscopy P. Ramamurthy 2001
[b-Cyclodextrin](1).[ADR(4)] 2.90 0.75 Fluorescence spectroscopy P. Ramamurthy 2001
[b-Cyclodextrin](1).[ADR(5)] 2.75 1.41 Fluorescence spectroscopy P. Ramamurthy 2001
[b-Cyclodextrin](1).[Na hexanoate] 1.53 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[Na heptanoate] 2.04 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[Na octanoate] 2.57 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[Na nonanoate] 2.81 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[Na decanoate] 2.87 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[Na dodecanoate] 3.20 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[di-Na dodecylphosphate] 3.59 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[di-Na 4-hexyl 3-sulfonatosuccinate] 2.32 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[di-Na 4-heptyl 3-sulfonatosuccinate] 2.69 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[di-Na 4-octyl 3-sulfonatosuccinate] 2.88 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[di-Na 4-nonyl 3-sulfonatosuccinate] 3.05 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[di-Na 4-decyl 3-sulfonatosuccinate] 3.15 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[Na dodecyl benzenesulfonate] 4.18 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[Na perfluorooctanoate] 3.65 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[Na dihexyl 3-sulfosuccinate] 2.53 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[Na dioctyl 3-sulfosuccinate] 3.45 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[Na cyclohexyl acetate] 2.69 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[Na cyclohexyl propanoate] 3.15 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[Na cyclohexyl butanoate] 3.23 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[Na cyclohexyl sulfamate] 2.36 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[cetylpiridinium chloride] 4.70 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[cetylpiridinium bromide] 4.60 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[cetyltrimethylammonium bromide] 4.30 25.0 Conductivity Vincent C. Reinsborough 1989
[b-Cyclodextrin](1).[cetyltrimethylammonium bromide] 4.83 isothermal titration calorimetry E. Wyn-Jones 1995
[b-Cyclodextrin](1).[cetyltrimethylammonium bromide] 4.82 surface tension method E. Wyn-Jones 1995
[b-Cyclodextrin](1).[cetyltrimethylammonium bromide] 4.85 potentiometry E. Wyn-Jones 1995
[b-Cyclodextrin](1).[cetyltrimethylammonium bromide] 4.78 E. Wyn-Jones 1995
[b-Cyclodextrin](1).[tetradecyltrimethylammonium bromide] 4.71 3.16 25.0 Potentiometric titration Toshihiro Tominaga 1994
[b-Cyclodextrin](1).[tetradecyltrimethylammonium bromide] 4.60 isothermal titration calorimetry E. Wyn-Jones 1995
[b-Cyclodextrin](1).[tetradecyltrimethylammonium bromide] 4.60 potentiometry E. Wyn-Jones 1995
[b-Cyclodextrin](1).[tetradecyltrimethylammonium bromide] 4.64 E. Wyn-Jones 1995
[b-Cyclodextrin](1).[L-phenylalanineamide+] 1.34 0.30 5.01 25.0 Titration calorimetry Robert N. Goldberg 1994
[b-Cyclodextrin](1).[L-phenylalanineamide0] 2.03 0.48 10.02 25.0 Titration calorimetry Robert N. Goldberg 1994
[b-Cyclodextrin](1).[(S)-(+)-2-butanol] 1.30 0.70 6.9 25.0 Titration calorimetry Robert N. Goldberg 1994
[b-Cyclodextrin](1).[(R)-(-)-2-butanol] 1.11 0.60 6.9 25.0 Titration calorimetry Robert N. Goldberg 1994
[b-Cyclodextrin](1).[(+/-)-2-butanol] 1.11 0.60 6.9 25.0 Titration calorimetry Robert N. Goldberg 1994
[b-Cyclodextrin](1).[(S)-(+)-2-pentanol] 1.51 1.04 6.9 25.0 Titration calorimetry Robert N. Goldberg 1994
[b-Cyclodextrin](1).[(R)-(-)-2-pentanol] 1.52 1.08 6.9 25.0 Titration calorimetry Robert N. Goldberg 1994
[b-Cyclodextrin](1).[(R)-(-)-2-hexanol] 2.07 1.79 6.9 25.0 Titration calorimetry Robert N. Goldberg 1994
[b-Cyclodextrin](1).[triclopyr butoxy ethyl ester] 3.21 UV-Vis spectroscopy Manohar Ramchandra Sawant 2006
[b-Cyclodextrin](1).[4,4’-bipyridine] 2.01 25.0 stopped-flow spectrophotometry R.Prado-Gotor 2006
[b-Cyclodextrin](1).[ferrocene] 2.71 25.0 induced circular dichroism Udo H.Brinker 2006
[b-Cyclodextrin](1).[ferrocene] 1.78 25.0 cyclic voltametric titration Udo H.Brinker 2006
[b-Cyclodextrin](1).[ferrocene] 1.70 25.0 polarimetry Udo H.Brinker 2006
[b-Cyclodextrin](1).[ferrocenyl azide] 2.26 0.70 25.0 induced circular dichroism Udo H.Brinker 2006
[b-Cyclodextrin](1).[ferrocenyl azide] 2.28 1.30 25.0 UV-Vis spectroscopy Udo H.Brinker 2006
[b-Cyclodextrin](1).[ferrocenyl azide] 0.70 25.0 NMR spectroscopy Udo H.Brinker 2006
[b-Cyclodextrin](1).[1-adamantanamine] 3.96 25.0 steady-state fluorescence spectroscopy; NMR Qing-Xiang Guo 2002
[b-Cyclodextrin](1).[bisphenol F] 3.80 6.0 UV-Vis spectroscopy, fluorescence spectroscopy Nansheng Deng 2006
[b-Cyclodextrin](1).[bisphenol A] 3.76 6.0 UV-Vis and fluorescence spectroscopy Nansheng Deng 2005
[b-Cyclodextrin](1).[bisphenol A] 4.26 3.60 7.0 fluorescence spectroscopy Nansheng Deng 2006
[b-Cyclodextrin](1).[bisphenol E] 3.89 6.0 UV-Vis and fluorescence spectroscopy Nansheng Deng 2006
[b-Cyclodextrin](1).[simvastatin] 2.92 25.0 UV spectrophotometry Ziyang Liu 2005
[b-Cyclodextrin](1).[meso-tetrakis(4-N-ethylpyridiumyl) porphyrin] 2.74 7.61 20.0 UV-vis and fluorescence spectroscopy Shuang Shaomin 2005
[b-Cyclodextrin](1).[meso-tetrakis(4-N-methylpyridiumyl) porphyrin] 5.48 7.61 20.0 UV-vis and fluorescence spectroscopy Shuang Shaomin 2005
[b-Cyclodextrin](1).[buthylphenyilalanine] 4.00 7.0 25.0 circular dichroism Ronald Breslow 2003
[b-Cyclodextrin](1).[4-amino-phthalimide] 2.32 fluorescence spectroscopy Véronique Wintgens 2004
[b-Cyclodextrin](1).[AP-Me] 2.06 23.0 absorption and fluorescence spectroscopy Véronique Wintgens 2004
[b-Cyclodextrin](1).[AP-nPr] 2.68 23.0 absorption and fluorescence spectroscopy Véronique Wintgens 2004
[b-Cyclodextrin](1).[AP-isBut] 3.15 23.0 absorption and fluorescence spectroscopy Véronique Wintgens 2004
[b-Cyclodextrin](1).[AP-tBut] 3.49 23.0 absorption and fluorescence spectroscopy Véronique Wintgens 2004
[b-Cyclodextrin](1).[AP-cHex] 3.79 23.0 absorption and fluorescence spectroscopy Véronique Wintgens 2004
[b-Cyclodextrin](1).[AP-1Ada] 4.28 23.0 absorption and fluorescence spectroscopy Véronique Wintgens 2004
[b-Cyclodextrin](1).[1-adamantane carboxylic acid] 5.48 flow microcalorimetry, pH potentiometric measurements, spectral displacement methods Véronique Wintgens 2005
[b-Cyclodextrin](1).[sodium 1-adamantene carboxylate] 4.26 flow microcalorimetry, pH potentiometric measurements, spectral displacement methods Véronique Wintgens 2005
[b-Cyclodextrin](1).[poly(N-isopropylacrylamide)-Ada/1.4] 3.06 fluorimetry Véronique Wintgens 2005
[b-Cyclodextrin](2).[meso-tetraphenylporphyrin] 2.68 20.0 fluorescence spectroscopy Ke’an Li 2002
[b-Cyclodextrin](1).[1-octanol] 2.60 non-electrochemical methods M. Soledad Ureta-Zanartu 2004
[b-Cyclodextrin](1).[1-octanol] 2.74 2.11 differential pulse voltammetry M. Soledad Ureta-Zanartu 2004
[b-Cyclodextrin](1).[fenoxaprop-p-ethyl] 2.70 6.0 25.0 differential scanning calorimetry, infrared spectroscopy, X-ray diffraction Weiping Liu 2005
[b-Cyclodextrin](1).[Ponceau SX] 5.41 23.0 electrospray ionization mass spectrometry, Uv-vis and fluorescence spectroscopy Hanqi Zhang 2006
[b-Cyclodextrin](1).[Allura Red AC] 5.19 23.0 electrospray ionization mass spectrometry, Uv-vis and fluorescence spectroscopy Hanqi Zhang 2006
[b-Cyclodextrin](1).[Tartrazine] 3.95 23.0 electrospray ionization mass spectrometry, Uv-vis and fluorescence spectroscopy Hanqi Zhang 2006
[b-Cyclodextrin](1).[Orange II] 4.40 23.0 electrospray ionization mass spectrometry, Uv-vis and fluorescence spectroscopy Hanqi Zhang 2006
[b-Cyclodextrin](0.5).[Orange II] 6.76 23.0 electrospray ionization mass spectrometry, Uv-vis and fluorescence spectroscopy Hanqi Zhang 2006
[b-Cyclodextrin](1).[2-naphthol] 2.79 11.0 25.0 Infrared spectroscopy Christopher H. Evans 2005
[b-Cyclodextrin](1).[2-naphthol] 3.29 25.0 Infrared spectroscopy Christopher H. Evans 2005
[b-Cyclodextrin](2).[starch-binding domain(SBD) of glucoamylase ] 4.74 3.60 4.5 27.0 titration calorimetry Bent W. Sigurskjold 1994
[b-Cyclodextrin](2).[glucoamylase G1] 4.74 3.48 4.5 27.0 titration calorimetry Bent W. Sigurskjold 1994
[b-Cyclodextrin](1).[dodecyltrimethylammonium bromide] 3.38 2.78 25.0 computerized electrical conductivity technique Emilio Aicart 1995
[b-Cyclodextrin](1).[dodecyltrimethylammonium bromide] 4.26 Electromotive force E. Wyn-Jones 1995
[b-Cyclodextrin](1).[dodecyltrimethylammonium bromide] 4.37 isothermal titration calorimetry E. Wyn-Jones 1995
[b-Cyclodextrin](1).[dodecyltrimethylammonium bromide] 3.16 25.0 Emilia Iglesias 1998
[b-Cyclodextrin](1).[dodecyltrimethylammonium bromide] 3.48 25.0 NMR, mass spectrometry Emilia Iglesias 1998
[b-Cyclodextrin](1).[L-tyrosine] 5.17 11.3 25.0 microcalorimetry Giuseppina Castronuovo 1995
[b-Cyclodextrin](1).[L-tyrosine] 1.25 0.51 9.88 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[2,6-Diaminohexanoic acid] 4.18 3.30 11.3 25.0 microcalorimetry Giuseppina Castronuovo 1995
[b-Cyclodextrin](1).[sodium perfluorooctanoate] 3.65 10.0 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](1).[perfluoroalkylamide, "1e"] 5.38 10.0 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](1).[perfluoroalkylamide, "1e"] 5.00 4.00 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](1).[2-(2’-hydroxyphenyl)benzimidazole] 2.12 7.0 25.0 fluorescence spectroscopy Isiah M.Warner 1996
[b-Cyclodextrin](1).[2-(2’-hydroxyphenyl)benzimidazole] 1.72 7.0 25.0 induced circular dichroism Isiah M.Warner 1996
[b-Cyclodextrin](1).[2-(2¢-hydroxyphenyl)benzoxazole] 2.53 7.0 25.0 fluorescence spectroscopy Isiah M.Warner 1996
[b-Cyclodextrin](1).[2-(2¢-hydroxyphenyl)benzoxazole] 2.36 7.0 25.0 induced circular dichroism Isiah M.Warner 1996
[b-Cyclodextrin](1).[2-(2’-hydroxyphenyl)benzothiazole] 2.34 7.0 25.0 fluorescence spectroscopy Isiah M.Warner 1996
[b-Cyclodextrin](1).[2-(2’-hydroxyphenyl)benzothiazole] 1.98 7.0 25.0 induced circular dichroism Isiah M.Warner 1996
[b-Cyclodextrin](1).[2-(2’-methoxyphenyl)benzothiazole] 2.59 7.0 25.0 fluorescence spectroscopy Isiah M.Warner 1996
[b-Cyclodextrin](1).[2-(2’-methoxyphenyl)benzothiazole] 2.49 7.0 25.0 induced circular dichroism Isiah M.Warner 1996
[b-Cyclodextrin](1).[calcichrome] 2.58 1.90 25.0 NMR spectroscopy Bo-Long Poh 1996
[b-Cyclodextrin](1).[bupivacaine] 2.05 0.80 25.0 HPLC Gilles Dollo 1996
[b-Cyclodextrin](1).[bupivacaine] 1.94 37.0 HPLC Gilles Dollo 1996
[b-Cyclodextrin](1).[etidocaine] 1.58 0.20 25.0 HPLC Gilles Dollo 1996
[b-Cyclodextrin](1).[etidocaine] 1.43 0.23 37.0 HPLC Gilles Dollo 1996
[b-Cyclodextrin](1).[lidocaine] 1.41 -0.22 25.0 HPLC Gilles Dollo 1996
[b-Cyclodextrin](1).[lidocaine] 1.37 0.08 37.0 HPLC Gilles Dollo 1996
[b-Cyclodextrin](1).[mepivacaine] 1.71 0.11 25.0 HPLC Gilles Dollo 1996
[b-Cyclodextrin](1).[mepivacaine] 1.73 0.30 37.0 HPLC Gilles Dollo 1996
[b-Cyclodextrin](1).[prilocaine] 1.98 0.04 25.0 HPLC Gilles Dollo 1996
[b-Cyclodextrin](1).[prilocaine] 1.83 0.52 37.0 HPLC Gilles Dollo 1996
[b-Cyclodextrin](1).[3-cyanophenol] 1.56 1.30 3.05 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[b-Cyclodextrin](1).[3-cyanophenolate ion] 2.69 10.28 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[b-Cyclodextrin](1).[4-cyanophenol] 2.52 1.48 3.05 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[b-Cyclodextrin](1).[4-cyanophenolate] 2.36 1.48 10.28 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[b-Cyclodextrin](1).[4-nitrophenolate ion] 2.51 1.78 10.28 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[b-Cyclodextrin](1).[4-bromophenol] 2.49 1.00 3.5 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[b-Cyclodextrin](1).[4-bromophenolate ion] 3.04 10.28 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[b-Cyclodextrin](1).[4-methoxyphenol] 1.90 1.60 4.0 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[b-Cyclodextrin](1).[4-methoxyphenolate ion] 1.34 10.6 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[b-Cyclodextrin](1).[p-nitrophenyl isonicotinate] 2.23 9.5 25.0 NMR spectroscopy Paolo Scrimin 1997
[b-Cyclodextrin](1).[p-nitrophenyl nicotinate] 2.23 9.5 25.0 NMR spectroscopy Paolo Scrimin 1997
[b-Cyclodextrin](1).[p-nitrophenyl urocanoate] 2.32 10.5 25.0 NMR spectroscopy Paolo Scrimin 1997
[b-Cyclodextrin](1).[m-nitrophenyl isonicotinate] 2.20 9.5 25.0 NMR spectroscopy Paolo Scrimin 1997
[b-Cyclodextrin](1).[8-anilino-1-naphthalene sodium sulphonate] 1.95 1.11 7.0 25.0 fluorescence emission spectroscopy Emilio Aicart 1997
[b-Cyclodextrin](1).[clofibrate] 3.12 25.0 NMR spectroscopy S. Anguiano-Igea 1997
[b-Cyclodextrin](1).[sodium octyl sulfonate] 3.40 2.36 50.0 NMR spectroscopy Hanqing Wang 1997
[b-Cyclodextrin](1).[sodium dodecyl sulfonate] 3.47 2.74 50.0 NMR spectroscopy Hanqing Wang 1997
[b-Cyclodextrin](1).[sodium hexadecyl sulfonate] 3.99 2.77 50.0 NMR spectroscopy Hanqing Wang 1997
[b-Cyclodextrin](1).[m-cresol purple] 3.05 7.0 25.0 fluorescence spectroscopy Paul J. Smith 1998
[b-Cyclodextrin](1).[mono-substitued benzene, H] 2.29 0.95 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[mono-substitued benzene, H] 2.08 1.00 25.0 Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[mono-substitued benzene, H] 2.23 1.04 Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[methylbenzene] 2.33 1.08 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[methylbenzene] 2.15 1.00 25.0 Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[ethylbenzene] 2.59 1.18 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[ethylbenzene] 2.52 1.00 25.0 Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[mono-substitued benzene, C2H] 2.36 1.11 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[mono-substitued benzene, OCH3] 2.32 1.00 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[mono-substitued benzene, OC2H5] 2.49 1.18 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[mono-substitued benzene, OC2H5] 2.46 1.18 Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[mono-substitued benzene, CH2OH] 2.16 0.78 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[mono-substitued benzene, CH2Cl] 2.45 1.00 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[mono-substitued benzene, CHO] 2.18 0.85 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[mono-substitued benzene, COCH3] 2.27 0.90 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[mono-substitued benzene, COOCH3] 2.50 1.04 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[mono-substitued benzene, COOC2H5] 2.73 1.20 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[cyanobenzene] 2.23 0.90 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[aminobenzene] 1.93 0.40 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[mono-substitued benzene, NHCH3] 2.12 0.48 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[mono-substitued benzene, NHCH3] 1.68 0.38 Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[mono-substitued benzene, NHC2H5] 2.34 0.95 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[mono-substitued benzene, N(CH3)2] 2.40 1.00 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[mono-substitued benzene, N(CH3)2] 2.36 1.00 Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[mono-substitued benzene, NHCOCH3] 2.20 0.78 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[fluorobenzene] 1.96 1.30 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[fluorobenzene] 1.85 1.48 25.0 Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[chlorobenzene] 2.27 1.08 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[chlorobenzene] 2.20 1.00 25.0 Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[bromobenzene] 2.51 1.18 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[bromobenzene] 2.49 1.00 25.0 Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[iodobenzene] 2.93 1.30 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[iodobenzene] 2.90 1.00 25.0 Qing-Xiang Guo 1998
[b-Cyclodextrin](1).[calcium acetylhomotaurinate] 3.26 2.30 30.0 NMR spectroscopy Irina N. Topchieva 1998
[b-Cyclodextrin](1).[calcium acetylhomotaurinate] 3.03 1.30 50.0 NMR spectroscopy Irina N. Topchieva 1998
[b-Cyclodextrin](1).[calcium acetylhomotaurinate] 2.93 1.60 70.0 NMR spectroscopy Irina N. Topchieva 1998
[b-Cyclodextrin](1).[diflunisal] 3.18 2.00 7.4 absorption spectroscopy, induced circular dichroism Sandra Monti 1999
[b-Cyclodextrin](1).[fenbufen] 3.41 2.18 7.4 absorption spectroscopy, induced circular dichroism Sandra Monti 1999
[b-Cyclodextrin](1).[N-phenylphenothiazine] 2.10 1.00 25.0 UV-vis spectroscopy Qing-Xiang Guo 1999
[b-Cyclodextrin](1).[N-benzylphenothiazine] 2.49 1.49 25.0 UV-vis spectroscopy Qing-Xiang Guo 1999
[b-Cyclodextrin](1).[N-phenethylphenothiazine] 2.32 1.28 25.0 UV-vis spectroscopy Qing-Xiang Guo 1999
[b-Cyclodextrin](1).[p-nitrofluoroacetanilide] 2.00 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](1).[perfluoroalkylamide, "1a"] 3.46 2.00 10.0 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](1).[perfluoroalkylamide, "1a"] 2.67 1.60 3.0 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](1).[perfluoroalkylamide, "1b"] 3.51 2.00 10.0 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](1).[perfluoroalkylamide, "1b"] 3.30 2.00 3.0 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](1).[perfluoroalkylamide, "1c"] 3.20 2.00 10.0 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](1).[perfluoroalkylamide, "1c"] 3.79 2.00 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](1).[perfluoroalkylamide, "1d"] 4.80 3.00 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](1).[perfluoroalkylamide, "1f"] 4.92 3.95 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](2).[perfluoroalkylamide, "1a"] 1.61 0.70 10.0 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](2).[perfluoroalkylamide, "1a"] 2.26 1.48 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](2).[perfluoroalkylamide, "1b"] 1.93 0.78 10.0 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](2).[perfluoroalkylamide, "1b"] 1.69 0.90 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](2).[perfluoroalkylamide, "1c"] 1.36 0.48 10.0 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](2).[perfluoroalkylamide, "1c"] 1.48 0.85 3.0 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](2).[perfluoroalkylamide, "1d"] 2.00 1.00 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](2).[perfluoroalkylamide, "1e"] 1.30 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](2).[p-nitrofluoroacetanilide] 1.20 0.78 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](1).["3"] 3.00 2.00 10.0 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin](2).["3"] 1.95 1.48 10.0 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[b-Cyclodextrin].[pullulanase] 5.85 UV difference spectroscopy, flow calorimetry Bent W. Sigurskjold 1994
[b-Cyclodextrin].[starch-binding domain(SBD) of glucoamylase ] 5.77 titration calorimetry Bent W. Sigurskjold 1994
[b-Cyclodextrin].[glucoamylase G1] 4.75 Scatchard analysis Bent W. Sigurskjold 1994
[b-Cyclodextrin].[glucoamylase G1] 5.64 titration calorimetry Bent W. Sigurskjold 1994
[b-Cyclodextrin](1).[2-nitrophenol] 2.16 1.00 3.5 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[b-Cyclodextrin](1).[2-nitrophenolate ion] 2.00 0.70 10.28 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[b-Cyclodextrin](1).[3-nitrophenol] 2.11 1.00 3.5 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[b-Cyclodextrin](1).[3-nitrophenolate ion] 1.88 1.00 10.28 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[b-Cyclodextrin](1).[phenolate ion] 1.18 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[b-Cyclodextrin](1).[10-methyl-12H-benzo(a)phenothiazine] 1.15 0.85 20.0 fluorescence spectroscopy Jean-Jacques Aaron 2006
[b-Cyclodextrin].[sodium dodecyl sulfate] 3.51 fluorescence spectroscopy Hanqing Wang 1997
[b-Cyclodextrin](2).[tetradecyltrimethylammonium bromide] 3.49 isothermal titration calorimetry E. Wyn-Jones 1995
[b-Cyclodextrin](2).[tetradecyltrimethylammonium bromide] 1.75 potentiometry E. Wyn-Jones 1995
[b-Cyclodextrin](2).[tetradecyltrimethylammonium bromide] 2.07 E. Wyn-Jones 1995
[b-Cyclodextrin](2).[cetyltrimethylammonium bromide] 3.98 isothermal titration calorimetry E. Wyn-Jones 1995
[b-Cyclodextrin](2).[cetyltrimethylammonium bromide] 2.60 surface tension method E. Wyn-Jones 1995
[b-Cyclodextrin](2).[cetyltrimethylammonium bromide] 2.10 potentiometry E. Wyn-Jones 1995
[b-Cyclodextrin](2).[cetyltrimethylammonium bromide] 2.59 E. Wyn-Jones 1995
[b-Cyclodextrin](1).[dodecylpyridinium bromide] 4.40 Electromotive force E. Wyn-Jones 1995
[b-Cyclodextrin](1).[dodecylpyridinium bromide] 4.27 isothermal titration calorimetry E. Wyn-Jones 1995
[b-Cyclodextrin](1).[tert-butyl group on polymer chain] 2.53 NMR spectroscopy Akira Harada 1997
[b-Cyclodextrin](1).[n-hexyl group on polymer chain] 2.04 NMR spectroscopy Akira Harada 1997
[b-Cyclodextrin](1).[isooctyl group on polymer chain] 2.47 NMR spectroscopy Akira Harada 1997
[b-Cyclodextrin](1).[dodecyl group on polymer chain] 2.82 NMR spectroscopy Akira Harada 1997
[b-Cyclodextrin](1).[coumatetralyl] 2.75 1.62 20.0 fluorescence spectroscopy Jean-Jacques Aaron 1998
[b-Cyclodextrin](1).[coumatetralyl] 2.83 synchronous fluorescence measurements Jean-Jacques Aaron 1998
[b-Cyclodextrin](1).[pirimiphos-methyl] 2.23 1.53 10.0 20.0 fluorescence spectroscopy Jean-Jacques Aaron 1998
[b-Cyclodextrin](1).[chlorpyriphos] 1.95 1.45 4.0 20.0 fluorescence spectroscopy, photochemically induced fluorescence method Jean-Jacques Aaron 1998
[b-Cyclodextrin](1).[deltamethrin] 2.80 2.02 11.0 20.0 fluorescence spectroscopy, photochemically induced fluorescence method Jean-Jacques Aaron 1998
[b-Cyclodextrin](1).[fenvalerate] 2.50 1.79 10.0 20.0 fluorescence spectroscopy, photochemically induced fluorescence method Jean-Jacques Aaron 1998
[b-Cyclodextrin](1).[ricobendazole] 2.03 differential scanning calorimetry Natalie J. Medlicott 2005
[b-Cyclodextrin](1).[dimethyl terephthalate] 2.95 25.0 fluorescence spectroscopy Francisco Mendicuti 2004
[b-Cyclodextrin](1).[dimethyl terephthalate] 3.06 1.77 5.0 fluorescence spectroscopy Francisco Mendicuti 2004
[b-Cyclodextrin](1).[dimethyl terephthalate] 2.98 1.70 15.0 fluorescence spectroscopy Francisco Mendicuti 2004
[b-Cyclodextrin](1).[dimethyl terephthalate] 2.92 1.76 35.0 fluorescence spectroscopy Francisco Mendicuti 2004
[b-Cyclodextrin](1).[dimethyl terephthalate] 2.87 1.68 45.0 fluorescence spectroscopy Francisco Mendicuti 2004
[b-Cyclodextrin](1).[dimethyl isophthalate] 2.48 25.0 fluorescence spectroscopy Francisco Mendicuti 2004
[b-Cyclodextrin](1).[dimethyl isophthalate] 2.43 1.26 5.0 fluorescence spectroscopy Francisco Mendicuti 2004
[b-Cyclodextrin](1).[dimethyl isophthalate] 2.48 1.59 15.0 fluorescence spectroscopy Francisco Mendicuti 2004
[b-Cyclodextrin](1).[dimethyl isophthalate] 2.55 1.51 35.0 fluorescence spectroscopy Francisco Mendicuti 2004
[b-Cyclodextrin](1).[dimethyl isophthalate] 2.69 2.05 45.0 fluorescence spectroscopy Francisco Mendicuti 2004
[b-Cyclodextrin](1).[dimethyl phthalate] 1.84 25.0 fluorescence spectroscopy Francisco Mendicuti 2004
[b-Cyclodextrin](1).[dimethyl phthalate] 1.97 1.26 5.0 fluorescence spectroscopy Francisco Mendicuti 2004
[b-Cyclodextrin](1).[dimethyl phthalate] 1.91 1.20 15.0 fluorescence spectroscopy Francisco Mendicuti 2004
[b-Cyclodextrin](1).[dimethyl phthalate] 1.75 1.23 35.0 fluorescence spectroscopy Francisco Mendicuti 2004
[b-Cyclodextrin](1).[dimethyl phthalate] 1.48 1.48 45.0 fluorescence spectroscopy Francisco Mendicuti 2004
[b-Cyclodextrin](1).[o-hydroxybenzoic acid] 3.06 2.08 15.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[o-hydroxybenzoic acid] 2.97 1.95 20.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[o-hydroxybenzoic acid] 2.89 1.90 25.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[o-hydroxybenzoic acid] 2.80 1.78 30.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[o-hydroxybenzoic acid] 2.65 1.60 40.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[o-hydroxybenzoic acid] 2.85 25.0 Emilio Aicart 1999
[b-Cyclodextrin](1).[o-hydroxybenzoate] 2.08 1.30 15.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[o-hydroxybenzoate] 2.04 1.30 20.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[o-hydroxybenzoate] 1.95 1.30 25.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[o-hydroxybenzoate] 1.85 1.18 30.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[o-hydroxybenzoate] 1.65 1.00 40.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[o-hydroxybenzoate] 1.71 1.5 25.0 flow-injection dynamic dialysis technique Emilio Aicart 1999
[b-Cyclodextrin](1).[o-hydroxybenzoate] 2.02 25.0 speed of sound and conductivity experiments Emilio Aicart 1999
[b-Cyclodextrin](1).[m-hydroxybenzoic acid] 2.92 1.90 15.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[m-hydroxybenzoic acid] 2.81 1.78 20.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[m-hydroxybenzoic acid] 2.72 1.70 25.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[m-hydroxybenzoic acid] 2.65 1.60 30.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[m-hydroxybenzoic acid] 2.46 1.48 40.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[m-hydroxybenzoate] 1.74 1.08 15.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[m-hydroxybenzoate] 1.48 0.78 20.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[m-hydroxybenzoate] 1.46 0.78 25.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[m-hydroxybenzoate] 1.08 0.60 30.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[m-hydroxybenzoate] 0.70 40.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[p-hydroxybenzoic acid] 3.12 2.11 15.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[p-hydroxybenzoic acid] 3.05 2.04 20.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[p-hydroxybenzoic acid] 2.96 1.95 25.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[p-hydroxybenzoic acid] 2.90 1.90 30.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[p-hydroxybenzoic acid] 2.70 1.70 40.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[p-hydroxybenzoate] 2.00 1.30 15.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[p-hydroxybenzoate] 1.93 1.30 20.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[p-hydroxybenzoate] 1.88 1.18 25.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[p-hydroxybenzoate] 1.70 1.00 30.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[p-hydroxybenzoate] 1.68 1.00 40.0 pH Potentiometry Emilio Aicart 1999
[b-Cyclodextrin](1).[ethyl alcohol] -0.03 25.0 spectrophotometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[n-propyl alcohol] 0.57 25.0 spectrophotometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[n-propyl alcohol] 0.62 -0.82 11.6 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[n-butyl alcohol] 1.25 -0.49 25.0 spectrophotometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[n-pentyl alcohol] 1.80 25.0 spectrophotometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[n-pentyl alcohol] 1.86 0.79 11.6 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[n-hexyl alcohol] 2.36 0.71 25.0 spectrophotometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[n-hexyl alcohol] 2.32 0.89 11.6 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[n-heptil alcohol] 2.85 25.0 spectrophotometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[isopropyl alcohol] 0.58 25.0 spectrophotometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[isopropyl alcohol] 0.61 -0.59 11.6 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[isobutyl alcohol] 1.62 25.0 spectrophotometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[isopentyl alcohol] 2.25 25.0 spectrophotometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[2-butyl alcohol] 1.19 25.0 spectrophotometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[2-pentyl alcohol] 1.49 25.0 spectrophotometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[2-hexyl alcohol] 1.98 25.0 spectrophotometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[3-pentyl alcohol] 1.35 25.0 spectrophotometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[tert-butyl alcohol] 1.68 25.0 spectrophotometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[neopentyl alcohol] 2.76 25.0 spectrophotometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[cyclopentyl alcohol] 2.08 25.0 spectrophotometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[cyclohexyl alcohol] 2.74 0.79 25.0 spectrophotometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[cyclohexyl alcohol] 2.68 1.94 11.6 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[2-methoxy etylalcohol (MeOCH2CH2OH)] 0.22 25.0 spectrophotometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[Butyl sulfit ion (BuSO3-)] 1.05 -0.42 25.0 spectrophotometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[Pentyl sulfit ion (PentSO3-)] 1.78 25.0 conductometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[Hexyl sulfit ion (HexSO3-)] 2.25 25.0 conductometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[Heptyl sulfit ion (HeptSO3-)] 2.64 25.0 conductometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[Octyl sulfit ion (OctSO3-)] 3.01 25.0 conductometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[1-anilino-8-naphthalenesulfonate ion] 1.57 0.26 11.6 25.0 spectrofluorometry Oswald S.Tee 1996
[b-Cyclodextrin](1).[1-anilino-8-naphthalenesulfonate ion] 2.04 25.0 fluorescence spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[1-anilino-8-naphthalenesulfonate ion] 1.96 25.0 Oswald S.Tee 1996
[b-Cyclodextrin](1).[1-anilino-8-naphthalenesulfonate ion] 1.82 25.0 NMR titration Oswald S.Tee 1996
[b-Cyclodextrin](1).[n-butylamine] 2.13 11.6 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[n-butylamine] 1.00 11.6 25.0 dye displacement method Oswald S.Tee 1996
[b-Cyclodextrin](1).[n-butylamine] 0.48 11.6 25.0 indicator displacement method Oswald S.Tee 1996
[b-Cyclodextrin](1).[n-propylamine] 0.97 -0.37 11.6 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[n-propylamine] 0.95 11.6 25.0 dye displacement method Oswald S.Tee 1996
[b-Cyclodextrin](1).[n-pentylamine] 1.94 0.19 11.6 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[n-hexylamine] 2.58 1.59 11.6 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[n-heptylamine] 3.02 1.65 11.6 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[n-dimethyl-hexalamine] 2.18 0.92 11.6 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[cyclopentylamine] 1.87 1.06 11.6 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[cyclohexylamine] 2.74 1.86 11.6 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[morpholine] 1.25 0.29 11.6 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[morpholine] 1.23 11.6 25.0 indicator displacement method Oswald S.Tee 1996
[b-Cyclodextrin](1).[n-metylmorpholine] 1.63 0.57 11.6 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[n-etylmorpholine] 1.78 0.40 11.6 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[piperidine] 1.70 11.6 25.0 indicator displacement method Oswald S.Tee 1996
[b-Cyclodextrin](1).[L-valine] 0.59 -0.64 9.88 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[L-leucine] 0.97 -0.36 9.88 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[L-cysteine] 0.00 9.88 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[L-tryptophane] 1.35 -0.10 9.88 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[L-tryptophane] 2.35 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[b-Cyclodextrin](1).[DL-norvaline] -0.40 9.88 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[DL-norleucine] 0.80 0.08 9.88 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[prednisolone] 3.54 2.14 5.5 25.0 NMR spectroscopy Kim L.Larsen 2005
[b-Cyclodextrin](1).[prednisolone] 3.48 25.0 NMR, UV-vis spectroscopy, X-ray diffraction Kim L.Larsen 2005
[b-Cyclodextrin](1).[6a-methyl prednisolone] 3.01 1.48 5.5 25.0 NMR spectroscopy Kim L.Larsen 2005
[b-Cyclodextrin](1).[acetone] 0.44 -0.51 8.0 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[butan-2-one] 0.97 -0.76 8.0 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[pentan-2-one] 1.41 0.05 8.0 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[hexan-2-one] 1.79 0.42 8.0 25.0 displacement of a fluorescent probe Oswald S.Tee 1996
[b-Cyclodextrin](1).[heptan-2-one] 2.32 0.97 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[heptan-2-one] 2.31 1.31 25.0 fluorescent probe method Oswald S.Tee 1996
[b-Cyclodextrin](1).[octan-2-one] 2.76 1.00 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[pentan-3-one] 1.24 -0.15 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[hexan-3-one] 1.67 -0.05 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[heptan-3-one] 2.02 0.85 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[octan-3-one] 2.42 1.37 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[cyclobutanone] 0.97 -0.57 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[cyclopentanone] 1.71 0.19 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[cyclohexanone] 2.60 0.90 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[cycloheptanone] 3.20 2.32 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[cyclooctanone] 3.32 2.03 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[3-methylbutan-2-one] 1.82 0.25 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[3-methylpentan-2-one] 2.16 0.61 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[5-methylhexan-2-one] 2.50 1.01 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[3,3-dimethylbutan-2-one] 2.77 1.74 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[4-methylpentan-2-one] 1.90 0.54 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[heptan-4-one] 2.06 0.19 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[acetophenone] 2.09 0.92 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[heptan-2-ol] 2.63 0.57 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[hexan-3-ol] 1.75 -0.06 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[heptan-3-ol] 2.30 0.64 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[octan-3-ol] 2.91 1.78 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[1-phenylethanol] 2.02 0.44 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[b-Cyclodextrin](1).[ammonium 8-anilino-1-naphthalenesulphonic acid] 2.01 7.2 25.0 fluorescence spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[sodium 6-(p-toluidino)-2-naphthalenesulphonic acid] 3.56 7.2 25.0 fluorescence spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[N-methylaniline] 1.92 fluorescence spectroscopy Yu Liu 2001
[b-Cyclodextrin](1).[iodid ion] 0.66 0.15 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[b-Cyclodextrin](1).[nitrate ion (NO3-)] 1.75 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[b-Cyclodextrin](1).[perchlorate ion (ClO4-)] 0.91 0.23 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[b-Cyclodextrin](1).[fulminate ion (CNO-)] 0.23 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[b-Cyclodextrin](1).[thiocianate/rodanid ion (SCN-)] 0.73 0.15 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[b-Cyclodextrin](1).[dichromate ion(Cr2O72-)] 1.01 0.30 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[b-Cyclodextrin](1).[L-methionine] 0.18 0.11 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[b-Cyclodextrin](1).[aspartame] 2.32 1.62 NMR spectroscopy Soundar Divakar 1991
[b-Cyclodextrin](1).[Nile Blue] 3.28 7.0 25.0 UV-vis spectroscopy Hong-Yuan Chen 2002
[b-Cyclodextrin](1).[Nile Blue] 3.08 7.2 25.0 electrochemical characterization Hong-Yuan Chen 2002
[b-Cyclodextrin](1).[n-propanol] 0.57 7.2 25.0 UV-vis spectroscopy Yu Liu 1998
[b-Cyclodextrin](1).[n-butanol] 1.22 7.2 25.0 UV-vis spectroscopy Yu Liu 1998
[b-Cyclodextrin](1).[n-pentanol] 1.80 7.2 25.0 UV-vis spectroscopy Yu Liu 1998
[b-Cyclodextrin](1).[n-hexanol] 2.34 7.2 25.0 UV-vis spectroscopy Yu Liu 1998
[b-Cyclodextrin](1).[n-heptanol] 2.85 7.2 25.0 UV-vis spectroscopy Yu Liu 1998
[b-Cyclodextrin](1).[Ph-CH2CH2-ONO(1-phenylethyl nitrite)] 2.12 0.30 1.85 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[Ph-CH2CH2-ONO(1-phenylethyl nitrite)] 2.46 0.78 25.0 spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[Ph-CH2CH2-ONO(1-phenylethyl nitrite)] 2.07 0.90 13.3 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[Ph-CH2CH2-ONO(1-phenylethyl nitrite)] 2.04 0.90 13.6 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[Ph-CH2CH2-ONO(1-phenylethyl nitrite)] 2.05 0.78 12.7 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[Ph-CH2CH2-ONO(1-phenylethyl nitrite)] 2.07 0.30 13.0 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[Ph-CH2CH2-ONO(1-phenylethyl nitrite)] 2.45 1.20 11.35 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[(CH3)3C-ONO (tert-butyl nitrite)] 2.23 0.48 1.85 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[(CH3)3C-ONO (tert-butyl nitrite)] 2.17 0.30 4.89 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[(CH3)3C-ONO (tert-butyl nitrite)] 1.72 0.30 13.3 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[(CH3)3C-ONO (tert-butyl nitrite)] 2.16 0.70 11.35 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[Ph-CH-CH3-ONO(2-phenylethyl nitrite)] 2.56 0.85 1.85 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[Ph-CH-CH3-ONO(2-phenylethyl nitrite)] 2.45 1.04 4.89 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[Ph-CH-CH3-ONO(2-phenylethyl nitrite)] 1.93 0.85 13.6 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[Ph-CH-CH3-ONO(2-phenylethyl nitrite)] 2.03 0.85 13.3 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[Ph-CH-CH3-ONO(2-phenylethyl nitrite)] 1.96 1.04 13.0 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[C6H5-ONO] 2.72 0.95 1.85 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[C6H5-ONO] 2.74 1.32 4.89 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[CH3(CH2)2CH2-ONO] 1.70 0.30 1.85 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[CH3(CH2)4CH2-ONO] 2.15 0.48 1.85 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[Ph-CHCH2CH3-ONO] 2.72 1.18 4.89 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[pyrrolidine] 0.78 25.0 fluorescence spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[cyclohexyl nitrite] 2.45 1.57 13.3 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[cyclohexyl nitrite] 2.39 1.20 13.5 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[cyclohexyl nitrite] 2.44 1.56 13.0 25.0 UV-vis spectroscopy Emilia Iglesias 1998
[b-Cyclodextrin](1).[benzoate ion] 1.36 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[benzoate ion] 1.20 0.08 25.0 microcalorimetry Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[benzoate ion] 1.78 1.00 25.0 potentiometry Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[2-methyl benzoate ion] 1.11 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[2-methyl benzoate ion] 1.12 0.30 7.0 25.0 capillary electrophoresis(DAD) Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[3-methyl benzoate ion] 1.60 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[3-methyl benzoate ion] 1.68 -0.22 7.0 25.0 capillary electrophoresis(DAD) Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[4-methyl benzoate ion] 1.82 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[4-methyl benzoate ion] 2.00 7.0 25.0 capillary electrophoresis(DAD) Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[4-methyl benzoate ion] 2.04 25.0 potentiometry Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[2,4-dimethyl benzoate ion] 1.62 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[2,5-dimethyl benzoate ion] 1.43 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[3,5-dimethyl benzoate ion] 0.95 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[3,5-dimethoxy benzoate ion] 1.80 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[salicylate ion] 1.54 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[salicylate ion] 1.91 0.48 25.0 capillary electrophoresis(IAD) Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[salicylate ion] 1.70 0.85 25.0 capillary electrophoresis(DAD) Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[3-phenyl propionate ion] 1.90 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[4-tert-butyl benzoate ion] 2.58 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[4-tert-butyl benzoate ion] 4.26 25.0 microcalorimetry Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[ibuprofen anion] 3.40 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[ibuprofen anion] 3.46 2.70 25.0 UV-vis spectroscopy Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[ibuprofen anion] 3.11 0.70 37.0 capillary electrophoresis(DAD) Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[ibuprofen anion] 3.94 10.0 spectrofluorometry Graciela M. Escandar 2003
[b-Cyclodextrin](1).[ibuprofen anion] 3.96 25.0 spectrofluorometry Graciela M. Escandar 2003
[b-Cyclodextrin](1).[1-adamantane carboxylate ion] 2.70 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[1-adamantane carboxylate ion] 6.00 25.0 spectrophotometry Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[1-adamantane carboxylate ion] 4.30 25.0 microcalorimetry Wolfgang Zimmermann 1998
[b-Cyclodextrin](1).[palmoic acid] 2.32 0.30 10.8 25.0 fluorescence spectroscopy, circular dichroism Koji Kano 1991
[b-Cyclodextrin](1).[2,2'-dihydroxy-1,1'-dinaphthylmethane] 2.26 1.00 5.5 25.0 fluorescence spectroscopy, circular dichroism Koji Kano 1991
[b-Cyclodextrin](1).[3-hydroxy-2-naphthoic acid] 3.03 5.5 25.0 fluorescence spectroscopy, circular dichroism Koji Kano 1991
[b-Cyclodextrin](1).[4-(N,N-dimethylamino)benzonitrile] 1.01 -0.15 25.0 fluorescence spectroscopy Edwin Quinones 1999
[b-Cyclodextrin](1).[4-(N,N-dimethylamino)benzonitrile] 0.66 20.0 fluorescence spectroscopy Edwin Quinones 1999
[b-Cyclodextrin](1).[4-(N,N-dimethylamino)benzonitrile] 0.62 28.0 fluorescence spectroscopy Edwin Quinones 1999
[b-Cyclodextrin](1).[4-(N,N-dimethylamino)benzonitrile] 0.74 31.0 fluorescence spectroscopy Edwin Quinones 1999
[b-Cyclodextrin](1).[4-(N,N-dimethylamino)benzonitrile] 0.54 34.0 fluorescence spectroscopy Edwin Quinones 1999
[b-Cyclodextrin](1).[4-(N,N-dimethylamino)benzonitrile] 0.69 37.0 fluorescence spectroscopy Edwin Quinones 1999
[b-Cyclodextrin](1).[4-(N,N-dimethylamino)benzonitrile] 0.54 40.0 fluorescence spectroscopy Edwin Quinones 1999
[b-Cyclodextrin](1).[4-(N,N-dimethylamino)benzonitrile] 0.70 43.0 fluorescence spectroscopy Edwin Quinones 1999
[b-Cyclodextrin](1).[4-(N,N-dimethylamino)benzonitrile] 0.74 47.0 fluorescence spectroscopy Edwin Quinones 1999
[b-Cyclodextrin](1).[4-(N,N-dimethylamino)benzonitrile] 0.60 51.0 fluorescence spectroscopy Edwin Quinones 1999
[b-Cyclodextrin](1).[4-(N,N-dimethylamino)benzonitrile] 0.47 56.0 fluorescence spectroscopy Edwin Quinones 1999
[b-Cyclodextrin](1).[4-(N,N-dimethylamino)benzonitrile] 0.55 61.0 fluorescence spectroscopy Edwin Quinones 1999
[b-Cyclodextrin](1).[4-(N,N-dimethylamino)benzonitrile] 3.01 2.40 25.0 Edwin Quinones 1999
[b-Cyclodextrin](1).[6-p-toluidinylnaphthalene-2-sulphonate] 3.04 25.0 UV-vis spectroscopy Yannis L. Loukas 2000
[b-Cyclodextrin](1).[gentian violet] 2.52 1.85 7.5 25.0 UV-vis spectroscopy David Díaz 1999
[b-Cyclodextrin](1).[gentian violet] 1.65 25.0 UV-vis spectroscopy David Díaz 1999
[b-Cyclodextrin](1).[7-ferrocenyl-2,4,6-heptatrienal] 4.09 2.43 25.0 spectrophotometry Angel E. Kaifer 2000
[b-Cyclodextrin](1).[7-ferrocenyl-2,4,6-heptatrienol] 4.11 2.18 25.0 spectrophotometry Angel E. Kaifer 2000
[b-Cyclodextrin](1).[methyl red] 3.54 7.2 25.0 UV-vis spectroscopy Yu Liu 2002
[b-Cyclodextrin](2).[EG2RE (ethylene glycol-rhenium complex)] 3.28 2.48 7.0 25.0 NMR spectroscopy David N. Reinhoudt 2001
[b-Cyclodextrin](1).[C1C7V2+] 2.64 25.0 circular dichroism Joon Woo Park 2003
[b-Cyclodextrin](1).[methyloctyl viologen] 2.95 25.0 circular dichroism Joon Woo Park 2003
[b-Cyclodextrin](1).[C1C10V2+] 3.89 25.0 circular dichroism Joon Woo Park 2003
[b-Cyclodextrin](1).[C1C12V2+] 4.08 25.0 circular dichroism Joon Woo Park 2003
[b-Cyclodextrin](0.5).[Cu(II) ion] 39.20 Eugenijus Norkus 2004
[b-Cyclodextrin](1).[adamantylmethyl viologen] 3.86 2.60 25.0 circular dichroism Joon Woo Park 2002
[b-Cyclodextrin](1).[n-octylammonium] 2.88 25.0 Joon Woo Park 2002
[b-Cyclodextrin](1).[1-adamantanammonium] 3.93 25.0 spectrophotometry, pH potentiometry Joon Woo Park 2002
[b-Cyclodextrin](1).[PBNOH] 1.76 NMR spectroscopy Paul Tordo 2004
[b-Cyclodextrin](1).[a-phenyl-N-tert-butylnitrone] 2.07 NMR spectroscopy Paul Tordo 2004
[b-Cyclodextrin](1).[PBNdiOH] 1.51 NMR spectroscopy Paul Tordo 2004
[b-Cyclodextrin](1).[PBNtriOH] 1.54 NMR spectroscopy Paul Tordo 2004
[b-Cyclodextrin](1).[4-Me-PBNOH] 1.99 NMR spectroscopy Paul Tordo 2004
[b-Cyclodextrin](1).[4-MeO-PBNOH] 2.17 NMR spectroscopy Paul Tordo 2004
[b-Cyclodextrin](1).[4-Et-PBNOH] 3.03 NMR spectroscopy Paul Tordo 2004
[b-Cyclodextrin](1).[PEBNOH] 2.37 NMR spectroscopy Paul Tordo 2004
[b-Cyclodextrin](1).[1-adamantanol] 4.00 6.4 20.0 electrochemical masurements, cyclic voltammetry Marcin Majda 2000
[b-Cyclodextrin](1).[1-adamantane carboxylate] 4.30 25.0 pH titration Marcin Majda 2000
[b-Cyclodextrin](1).[o-fluorophenol] 1.53 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[m-fluorophenol] 1.57 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[p-fluorophenol] 1.48 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[o-iodophenol] 1.88 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[m-iodophenol] 2.08 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[p-iodophenol] 2.16 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[o-nitrophenol] 1.81 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[o-nitrophenol] 2.55 10.0 20.0 polarography Kazumi Fujimura 1986
[b-Cyclodextrin](1).[m-nitrophenol] 1.95 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[m-nitrophenol] 2.17 10.0 20.0 polarography Kazumi Fujimura 1986
[b-Cyclodextrin](1).[o-chlorophenol] 1.84 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[m-chlorophenol] 1.80 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[p-chlorophenol] 1.92 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[o-cresol] 1.92 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[p-cresol] 1.92 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[o-fluoroaniline] 1.32 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[m-fluoroaniline] 1.36 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[p-fluoroaniline] 1.95 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[o-iodoaniline] 1.82 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[m-iodoaniline] 2.03 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[p-iodoaniline] 2.20 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[o-nitroaniline] 0.97 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[m-nitroaniline] 1.41 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[p-nitroaniline] 1.63 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[o-chloroaniline] 1.78 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[m-chloroaniline] 1.79 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[p-chloroaniline] 2.01 23.0 reverse-phase liquid chromatography (RPLC) Kazumi Fujimura 1986
[b-Cyclodextrin](1).[dimethindene, S(+) enantiomer] 2.66 NMR spectroscopy Gottfried Blaschke 1998
[b-Cyclodextrin](1).[dimethindene, R(-) enantiomer] 2.70 NMR spectroscopy Gottfried Blaschke 1998
[b-Cyclodextrin](1).[2-naphthalenesulfonate] 5.37 0.07 7.2 25.0 calorimetric titration Yoshihisa Inoue 1993
[b-Cyclodextrin](1).[1-anilino-8-naphthalenesulfonate] 1.75 Yoshihisa Inoue 1993
[b-Cyclodextrin](1).[4-methylbenzylamine] 2.08 25.0 spectrophotometry Hans-Jürgen Buschmann 1997
[b-Cyclodextrin](1).[1,4-phenylene diamine] 1.14 25.0 spectrophotometry Hans-Jürgen Buschmann 1997
[b-Cyclodextrin](1).[Direct orange 39] 1.99 25.0 spectrophotometry Hans-Jürgen Buschmann 1997
[b-Cyclodextrin](1).[Direct orange 40] 2.10 25.0 spectrophotometry Hans-Jürgen Buschmann 1997
[b-Cyclodextrin](1).[Orange II.] 1.59 25.0 spectrophotometry Hans-Jürgen Buschmann 1997
[b-Cyclodextrin](1).[Orange IV.] 2.64 25.0 spectrophotometry Hans-Jürgen Buschmann 1997
[b-Cyclodextrin](1).[thioxanthone] 3.00 1.78 20.0 fluorescence spectroscopy Cornelia Bohne 2001
[b-Cyclodextrin](1).[thioxanthone] 1.85 1.60 25.0 absorption spectroscopy Cornelia Bohne 2001
[b-Cyclodextrin](1).[6-p-toluidinylnaphthalene-2-sulfonate] 3.04 25.0 Uv-vis spectrophotometry Yannis L. Loukas 2002
[b-Cyclodextrin](1).[pindolol] 2.07 12.1 17.0 spectrofluorimetry Miguel Sanchez 2003
[b-Cyclodextrin](1).[pindolol] 2.04 12.1 20.0 spectrofluorimetry Miguel Sanchez 2003
[b-Cyclodextrin](1).[pindolol] 1.99 12.1 25.0 spectrofluorimetry Miguel Sanchez 2003
[b-Cyclodextrin](1).[pindolol] 1.92 12.1 30.0 spectrofluorimetry Miguel Sanchez 2003
[b-Cyclodextrin](1).[alkyl-substitued hydroxyphenylazo derivative of sulfanilic acid; acid form] 3.30 4.6 25.0 Uv-vis absorption spectroscopy, circular dichroism Noboru Yoshida 1990
[b-Cyclodextrin](1).[alkyl-substitued hydroxyphenylazo derivative of sulfanilic acid; based form] 3.20 12.0 25.0 Uv-vis absorption spectroscopy, circular dichroism Noboru Yoshida 1990
[b-Cyclodextrin](1).[adamantanecarboxylate] 4.59 4.5 25.0 microcalorimetry, pH potentiometry Maurice R. Eftink 1985