[(h5-C5H5)Fe(h5-C5H4CH2N(CH3)2(CH2)12N-(CH3)2CH2h5-C5H4)Fe(h5-C5H5)]2+
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
None None SF_C743 None

SMILES:

Supramolecules

Namelog KSDpHT(°C)MethodRef
[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

[(h5-C5H5)Fe(h5-C5H4CH2N(CH3)2CH2(p-C6H4)CH2N(CH3)2CH2h5-C5H4)Fe(h5-C5H5)]2+
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
None None SF_C742 None

SMILES:

Supramolecules

Namelog KSDpHT(°C)MethodRef
[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

[(−)-(5R,6S)-7,8-didehydro-4,5-epoxy-3-methoxy-17-methyl-morphinan-6-ol]
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
299.36 4 1 1.44 SF_C998 None Not checked

SMILES: COc1ccc2C[C@@H]3[C@@H]4C=C[C@H](O)[C@@H]5Oc1c2[C@]45CCN3C

Supramolecules

Namelog KSDpHT(°C)MethodRef
[Heptakis(2,6-di-O-Methyl)-b-Cyclodextrin isomeric purity >80 %](1).[[(−)-(5R,6S)-7,8-didehydro-4,5-epoxy-3-methoxy-17-methyl-morphinan-6-ol]] 2.44 0.05 7.0 25.0 Potentiometry Lajos Barcza 2006
[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
[g-Cyclodextrin](1).[[(−)-(5R,6S)-7,8-didehydro-4,5-epoxy-3-methoxy-17-methyl-morphinan-6-ol]] 3.19 0.03 7.0 25.0 Potentiometry Lajos Barcza 2006

[(−)-(5R,6S)-7,8-didehydro-4,5-epoxy-3-methoxy-17-methyl-morphinan-6-ol]
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
299.36 4 1 1.44 SF_C998_p None Not checked

SMILES: COc1ccc2C[C@@H]3[C@@H]4C=C[C@H](O)[C@@H]5Oc1c2[C@]45CCN3C

Supramolecules

Namelog KSDpHT(°C)MethodRef

[(−)-(8S,9R)-6'-methoxy-cinchonanol]
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
None None SF_C1002 None

SMILES: [(−)-(8S,9R)-6'-methoxy-cinchonanol]

Supramolecules

Namelog KSDpHT(°C)MethodRef
[Heptakis(2,6-di-O-Methyl)-b-Cyclodextrin isomeric purity >80 %](1).[[(−)-(8S,9R)-6'-methoxy-cinchonanol]] 3.10 0.05 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

[1-(3,4-dimethoxy-benzyl)-6,7-dimethoxy-isoquinoline]
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
339.39 5 0 3.86 SF_C1000 None Not checked

SMILES: COc1ccc(Cc2nccc3cc(OC)c(OC)cc23)cc1OC

Supramolecules

Namelog KSDpHT(°C)MethodRef
[Heptakis(2,6-di-O-Methyl)-b-Cyclodextrin isomeric purity >80 %](1).[[1-(3,4-dimethoxy-benzyl)-6,7-dimethoxy-isoquinoline]] 1.99 0.05 7.0 25.0 Potentiometry Lajos Barcza 2006

[1-(3,4-dimethoxy-benzyl)-6,7-dimethoxy-isoquinoline]
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
339.39 5 0 3.86 SF_C1000_p None Not checked

SMILES: COc1ccc(Cc2nccc3cc(OC)c(OC)cc23)cc1OC

Supramolecules

Namelog KSDpHT(°C)MethodRef

[[1,4-dihydro-1-methyl-3-pyridinyl)carbonyl]-methyl[2S-(2a, 5a, 6b,)]-3,3-dimethyl-7-oxo-7-[(phenylacetyl)amino]-4-thia-azabicyclo[3.2.0] heptane-2-carboxylate
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
None None SF_C1825 None

SMILES:

Supramolecules

Namelog KSDpHT(°C)MethodRef
[2-O-(2-Hydroxy)propyl-b-Cyclodextrin](1).[[[1,4-dihydro-1-methyl-3-pyridinyl)carbonyl]-methyl[2S-(2a, 5a, 6b,)]-3,3-dimethyl-7-oxo-7-[(phenylacetyl)amino]-4-thia-azabicyclo[3.2.0] heptane-2-carboxylate] 2.97 4.66 40.0 HPLC-method Emil Pop 1991
[2-O-(2-Hydroxy)propyl-b-Cyclodextrin](1).[[[1,4-dihydro-1-methyl-3-pyridinyl)carbonyl]-methyl[2S-(2a, 5a, 6b,)]-3,3-dimethyl-7-oxo-7-[(phenylacetyl)amino]-4-thia-azabicyclo[3.2.0] heptane-2-carboxylate] 2.86 6.87 40.0 HPLC-method Emil Pop 1991
[2-O-(2-Hydroxy)propyl-b-Cyclodextrin](1).[[[1,4-dihydro-1-methyl-3-pyridinyl)carbonyl]-methyl[2S-(2a, 5a, 6b,)]-3,3-dimethyl-7-oxo-7-[(phenylacetyl)amino]-4-thia-azabicyclo[3.2.0] heptane-2-carboxylate] 2.89 8.36 40.0 HPLC-method Emil Pop 1991
[2-O-(2-Hydroxy)propyl-b-Cyclodextrin](1).[[[1,4-dihydro-1-methyl-3-pyridinyl)carbonyl]-methyl[2S-(2a, 5a, 6b,)]-3,3-dimethyl-7-oxo-7-[(phenylacetyl)amino]-4-thia-azabicyclo[3.2.0] heptane-2-carboxylate] 2.90 8.91 40.0 HPLC-method Emil Pop 1991
[2-O-(2-Hydroxy)propyl-b-Cyclodextrin](1).[[[1,4-dihydro-1-methyl-3-pyridinyl)carbonyl]-methyl[2S-(2a, 5a, 6b,)]-3,3-dimethyl-7-oxo-7-[(phenylacetyl)amino]-4-thia-azabicyclo[3.2.0] heptane-2-carboxylate] 2.91 6.45 70.0 HPLC-method Emil Pop 1991
[2-O-(2-Hydroxy)propyl-b-Cyclodextrin](1).[[[1,4-dihydro-1-methyl-3-pyridinyl)carbonyl]-methyl[2S-(2a, 5a, 6b,)]-3,3-dimethyl-7-oxo-7-[(phenylacetyl)amino]-4-thia-azabicyclo[3.2.0] heptane-2-carboxylate] 2.48 6.45 62.1 HPLC-method Emil Pop 1991
[2-O-(2-Hydroxy)propyl-b-Cyclodextrin](1).[[[1,4-dihydro-1-methyl-3-pyridinyl)carbonyl]-methyl[2S-(2a, 5a, 6b,)]-3,3-dimethyl-7-oxo-7-[(phenylacetyl)amino]-4-thia-azabicyclo[3.2.0] heptane-2-carboxylate] 2.26 6.45 51.5 HPLC-method Emil Pop 1991

a-(Diethoxyphosphinoximino)dicyclopropylmethane
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
245.26 5 0 3.48 VR_C102 None Not checked

SMILES: CCOP(OCC)ON=C(C1CC1)C2CC2

Supramolecules

Namelog KSDpHT(°C)MethodRef
[g-Cyclodextrin](1).[a-(Diethoxyphosphinoximino)dicyclopropylmethane] 3.17 35.0 HPLC Ekaterini Antoniadou-Vyza 1994
[g-Cyclodextrin](1).[a-(Diethoxyphosphinoximino)dicyclopropylmethane] 3.10 40.0 HPLC Ekaterini Antoniadou-Vyza 1994
[g-Cyclodextrin](1).[a-(Diethoxyphosphinoximino)dicyclopropylmethane] 2.94 45.0 HPLC Ekaterini Antoniadou-Vyza 1994
[g-Cyclodextrin](1).[a-(Diethoxyphosphinoximino)dicyclopropylmethane] 2.85 50.0 HPLC Ekaterini Antoniadou-Vyza 1994

a-Cyclodextrin
MW HBA HBD LogP CAS Suppliers Supplier IDs Storage ID Quantity Class PAINS
None None CY-1001 None

SMILES:

Supramolecules

Namelog KSDpHT(°C)MethodRef
[a-Cyclodextrin](1).[Fluorescein] 1.54 Induced circular dichroism absorption spectroscopy and steady-state and picosecond time resolved fluorescence spectroscopy Flamigni, Lucia 1993
[a-Cyclodextrin](1).[Erythrosine B] 1.30 Induced circular dichroism absorption spectroscopy and steady-state and picosecond time resolved fluorescence spectroscopy Flamigni, Lucia 1993
[a-Cyclodextrin](1).[N-adamantan-1'-ylpyrazinium cation] 1.88 6.8 25.0 1H NMR chemical shift titration and visible spectrophotometric titration Donald H. Macartney 1993
[a-Cyclodextrin](1).[(N-adamantan-1'-ylpyrazinium)pentacyanoferrate (II)-ion] 1.86 6.8 25.0 1H NMR chemical shift titration and visible spectrophotometric titration Donald H. Macartney 1993
[a-Cyclodextrin](1).[V+C11V+] 3.61 7.0 25.0 Potenciometric method Angel E. 1997
[a-Cyclodextrin](1).[C2V2+C11V2+C2] 2.36 7.0 25.0 Potenciometric method Angel E. 1997
[a-Cyclodextrin](1).[chenodeoxycholic acid] 3.96 8.3 25.0 Absorption spectroscopy Ueno, Akihiko 1997
[a-Cyclodextrin](1).[ursodeoxycholic acid] 4.97 8.3 25.0 Absorption spectroscopy Ueno, Akihiko 1997
[a-Cyclodextrin](1).[cholic acid] 2.83 8.3 25.0 Absorption spectroscopy Ueno, Akihiko 1997
[a-Cyclodextrin](1).[deoxycholic acid] 3.13 8.3 25.0 Absorption spectroscopy Ueno, Akihiko 1997
[a-Cyclodextrin](1).[hyodeoxycholic acid] 4.82 8.3 25.0 Absorption spectroscopy Ueno, Akihiko 1997
[a-Cyclodextrin](1).[1-adamantanol] 3.91 8.3 25.0 Absorption spectroscopy Ueno, Akihiko 1997
[a-Cyclodextrin](1).[2-adamantanol] 4.01 8.3 25.0 Absorption spectroscopy Ueno, Akihiko 1997
[a-Cyclodextrin](1).[1-adamantanecarboxylic acid] 3.97 8.3 25.0 Absorption spectroscopy Ueno, Akihiko 1997
[a-Cyclodextrin](1).[(+)-menthol] 3.00 8.3 25.0 Absorption spectroscopy Ueno, Akihiko 1997
[a-Cyclodextrin](1).[(-)-menthol] 2.96 8.3 25.0 Absorption spectroscopy Ueno, Akihiko 1997
[a-Cyclodextrin](1).[(+)-camphor] 2.66 8.3 25.0 Absorption spectroscopy Ueno, Akihiko 1997
[a-Cyclodextrin](1).[(-)-camphor] 2.59 8.3 25.0 Absorption spectroscopy Ueno, Akihiko 1997
[a-Cyclodextrin](1).[(+)-borneol] 3.40 8.3 25.0 Absorption spectroscopy Ueno, Akihiko 1997
[a-Cyclodextrin](1).[(-)-borneol] 3.39 8.3 25.0 Absorption spectroscopy Ueno, Akihiko 1997
[a-Cyclodextrin](1).[cyclohexanol] 2.42 8.3 25.0 Absorption spectroscopy Ueno, Akihiko 1997
[a-Cyclodextrin](1).[cyclohexanol] 1.92 0.60 7.0 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[cyclohexanol] 1.99 1.04 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[cyclooctanol] 2.56 8.3 25.0 Absorption spectroscopy Ueno, Akihiko 1997
[a-Cyclodextrin](1).[nerol] 2.46 8.3 25.0 Absorption spectroscopy Ueno, Akihiko 1997
[a-Cyclodextrin](1).[geraniol] 2.25 8.3 25.0 Absorption spectroscopy Ueno, Akihiko 1997
[a-Cyclodextrin](1).[imipramine] 2.11 1.30 25.0 conductivity measurments Aicart, E. 2001
[a-Cyclodextrin](1).[amitriptyline] 2.05 0.85 25.0 conductivity measurments Aicart, E. 2001
[a-Cyclodextrin](1).[5-benzoyl-1H-benzimidazol-2-yl-carbamic acide methyl ester] 2.40 7.2 25.0 Higuchi and Connors solubility method Shehatta, Ibrahim 2002
[a-Cyclodextrin](1).[5-benzoyl-1H-benzimidazol-2-yl-carbamic acide methyl ester] 2.18 7.5 25.0 Higuchi and Connors solubility method Shehatta, Ibrahim 2002
[a-Cyclodextrin].[phenol] 1.94 25.0 near-infrared spectrometry Tran, Chieu D. 2002
[a-Cyclodextrin](2.9).[1,4-diaminobutane] 1.18 0.14 25.0 NMR diffusion measurements Cohen, Yoram 2002
[a-Cyclodextrin](5.1).[1,6-diaminohexane] 1.81 0.07 25.0 NMR diffusion measurements Cohen, Yoram 2002
[a-Cyclodextrin](0.8).[1,8-diaminooctane] 2.83 0.21 25.0 NMR diffusion measurements Cohen, Yoram 2002
[a-Cyclodextrin](0.7).[1,10-diaminodecane] 4.13 0.30 25.0 NMR diffusion measurements Cohen, Yoram 2002
[a-Cyclodextrin](0.9).[1,12-diaminododecane] 3.85 0.27 25.0 NMR diffusion measurements Cohen, Yoram 2002
[a-Cyclodextrin](1.1).[1,8-diaminooctane hydrochloride] 1.87 0.15 25.0 NMR diffusion measurements Cohen, Yoram 2002
[a-Cyclodextrin](1.7).[1,10-diaminodecane hydrochloride] 3.34 0.19 25.0 NMR diffusion measurements Cohen, Yoram 2002
[a-Cyclodextrin](1).[1-b-D ribofuranosyl-1-H-1,2,4-triazole-3-carboxamide] 3.17 4.6 18.0 HPLC Kedzierewicz, F. 2005
[a-Cyclodextrin](1).[L-tryptophan] 1.79 0.03 7.2 25.0 Calorimetry Yu Liu 1998
[a-Cyclodextrin](1).[L-tryptophan] 2.01 1.06 8.0 18.0 UV-vis spectroscopy Andrzej Temeriusz 2006
[a-Cyclodextrin](1).[L-tryptophan] 4.28 7.0 25.0 microcalorimetry Giuseppina Castronuovo 1995
[a-Cyclodextrin](1).[L-tryptophan] 4.45 11.3 25.0 microcalorimetry Giuseppina Castronuovo 1995
[a-Cyclodextrin](1).[Disodium 2,7-naphthalenedisulfonate] 0.98 0.06 7.2 25.0 Calorimetry Yu Liu 1998
[a-Cyclodextrin](1).[Lauryl hexaoxyethylene] 3.30 2.30 25.0 Titration microcalorimetry Apryll M. Stalcup 2002
[a-Cyclodextrin](1.4).[Lauryl hexaoxyethylene] 5.81 4.90 25.0 Titration microcalorimetry Apryll M. Stalcup 2002
[a-Cyclodextrin](1).[Costa-type complex (R=n-C6H13)] 5.01 25.0 1H-NMR Hui-Lan Chen 2003
[a-Cyclodextrin](1).[Ebselen] 1.00 7.0 25.0 phase solubility Kaneto Uekama 2002
[a-Cyclodextrin](2).[Ebselen] 1.70 7.0 25.0 phase solubility Kaneto Uekama 2002
[a-Cyclodextrin](1).[N-(1-adamantylmethyl)-] 2.00 7.0 25.0 surface plasmon resonance (SPR) Susan E. Brown 2003
[a-Cyclodextrin](1).[N-octyl-] 3.23 1.90 7.0 25.0 surface plasmon resonance (SPR) Susan E. Brown 2003
[a-Cyclodextrin](1).[N-(4-tert-butyl benzyl)-] 2.00 7.0 25.0 surface plasmon resonance (SPR) Susan E. Brown 2003
[a-Cyclodextrin](1).[p-nitrophenol] 2.30 25.0 Potentiometric titration Kenneth A. Connors 1976
[a-Cyclodextrin](1).[p-nitrophenol] 2.46 25.0 Spectrophotometric method Kenneth A. Connors 1976
[a-Cyclodextrin](1).[p-nitrophenol] 2.24 3.0 30.0 NMR spectroscopy Soledad Penades 1993
[a-Cyclodextrin](1).[p-nitrophenol] 3.21 10.0 30.0 NMR spectroscopy Soledad Penades 1993
[a-Cyclodextrin](1).[p-nitrophenol] 3.20 7.4 23.0 UV-vis spectroscopy Jiri Horsky 1994
[a-Cyclodextrin](1).[p-nitrophenol] 2.22 0.05 7.0 30.0 NMR spectroscopy Yoshio Inoue 1992
[a-Cyclodextrin](1).[p-nitrophenol] 2.36 0.01 25.0 UV-vis spectroscopy Agustín G. Asuero 2006
[a-Cyclodextrin](1).[p-nitrophenol] 3.30 1.60 8.0 25.0 UV-vis spectroscopy Iwao Suzuki 2006
[a-Cyclodextrin](1).[p-nitrophenol] 2.18 0.48 3.0 25.0 UV and NMR spectroscopy Yoshihisa Matsui 1994
[a-Cyclodextrin](1).[p-nitrophenol] 2.16 0.70 3.5 25.0 UV and NMR spectroscopy Yoshihisa Matsui 1994
[a-Cyclodextrin](1).[p-nitrophenol] 2.17 0.30 4.0 25.0 UV and NMR spectroscopy Yoshihisa Matsui 1994
[a-Cyclodextrin](1).[p-nitrophenol] 3.27 1.38 10.0 25.0 UV and NMR spectroscopy Yoshihisa Matsui 1994
[a-Cyclodextrin](1).[p-nitrophenol] 3.27 1.30 10.4 25.0 UV and NMR spectroscopy Yoshihisa Matsui 1994
[a-Cyclodextrin](1).[p-nitrophenol] 3.27 1.30 11.0 25.0 UV and NMR spectroscopy Yoshihisa Matsui 1994
[a-Cyclodextrin](1).[p-nitrophenol] 3.38 2.48 11.0 25.0 capillary electrophoresis Daniel W. Armstrong 1996
[a-Cyclodextrin](1).[p-nitrophenol] 3.26 2.48 11.1 25.0 calorimetry Daniel W. Armstrong 1996
[a-Cyclodextrin](1).[p-nitrophenol] 3.36 11.0 25.0 UV spectroscopy Daniel W. Armstrong 1996
[a-Cyclodextrin](1).[p-nitrophenol] 2.83 10.0 25.0 NMR spectroscopy Daniel W. Armstrong 1996
[a-Cyclodextrin](1).[p-nitrophenol] 2.10 25.0 titration calorimetry Yannis L. Loukas 1997
[a-Cyclodextrin](1).[p-nitrophenol] 2.40 25.0 spectrophotometry Yannis L. Loukas 1997
[a-Cyclodextrin](1).[Benzoic acid] 3.15 25.0 Potentiometric titration Kenneth A. Connors 1976
[a-Cyclodextrin](1).[Benzoic acid] 3.02 1.1 25.0 Spectrophotometric method Kenneth A. Connors 1976
[a-Cyclodextrin](1).[Benzoic acid] 3.15 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,4-dimethoxybenzene] 0.93 7.0 12.0 absorption, circular dichroism, fluorescence, nanosecond transient absorption spectroscopy Gottfried Grabner; Sandra Monti 1996
[a-Cyclodextrin](1).[1,4-dimethoxybenzene] 1.11 7.0 22.0 absorption, circular dichroism, fluorescence, nanosecond transient absorption spectroscopy Gottfried Grabner; Sandra Monti 1996
[a-Cyclodextrin](1).[1,4-dimethoxybenzene] 1.53 7.0 35.0 absorption, circular dichroism, fluorescence, nanosecond transient absorption spectroscopy Gottfried Grabner; Sandra Monti 1996
[a-Cyclodextrin](1).[1,4-dimethoxybenzene] 1.60 7.0 48.0 absorption, circular dichroism, fluorescence, nanosecond transient absorption spectroscopy Gottfried Grabner; Sandra Monti 1996
[a-Cyclodextrin](2).[1,4-dimethoxybenzene] 3.26 7.0 12.0 absorption, circular dichroism, fluorescence, nanosecond transient absorption spectroscopy Gottfried Grabner; Sandra Monti 1996
[a-Cyclodextrin](2).[1,4-dimethoxybenzene] 2.80 7.0 22.0 absorption, circular dichroism, fluorescence, nanosecond transient absorption spectroscopy Gottfried Grabner; Sandra Monti 1996
[a-Cyclodextrin](2).[1,4-dimethoxybenzene] 2.16 7.0 35.0 absorption, circular dichroism, fluorescence, nanosecond transient absorption spectroscopy Gottfried Grabner; Sandra Monti 1996
[a-Cyclodextrin](2).[1,4-dimethoxybenzene] 1.78 7.0 48.0 absorption, circular dichroism, fluorescence, nanosecond transient absorption spectroscopy Gottfried Grabner; Sandra Monti 1996
[a-Cyclodextrin](1).[dimethyl phthalate] 2.93 7.0 25.0 self-assembled monolayer Hiromi Kitano 2000
[a-Cyclodextrin](1).[dimethyl phthalate] 4.62 7.0 25.0 UV-VIS Hiromi Kitano 2000
[a-Cyclodextrin](1).[diethyl phthalate] 2.96 7.0 25.0 self-assembled monolayer Hiromi Kitano 2000
[a-Cyclodextrin](1).[diethyl phthalate] 4.64 7.0 25.0 UV-VIS Hiromi Kitano 2000
[a-Cyclodextrin](1).[di-n-propyl phthalate] 3.09 7.0 25.0 self-assembled monolayer Hiromi Kitano 2000
[a-Cyclodextrin](1).[di-n-propyl phthalate] 4.68 7.0 25.0 UV-VIS Hiromi Kitano 2000
[a-Cyclodextrin](1).[di-n-butyl phthalate] 3.23 7.0 25.0 self-assembled monolayer Hiromi Kitano 2000
[a-Cyclodextrin](1).[di-n-butyl phthalate] 4.87 7.0 25.0 UV-VIS Hiromi Kitano 2000
[a-Cyclodextrin](1).[di-n-heptyl phthalate] 3.47 7.0 25.0 self-assembled monolayer Hiromi Kitano 2000
[a-Cyclodextrin](1).[di-n-heptyl phthalate] 5.18 7.0 25.0 UV-VIS Hiromi Kitano 2000
[a-Cyclodextrin](1).[di-2-ethylhexyl phthalate] 3.35 7.0 25.0 self-assembled monolayer Hiromi Kitano 2000
[a-Cyclodextrin](1).[di-2-ethylhexyl phthalate] 5.07 7.0 25.0 UV-VIS Hiromi Kitano 2000
[a-Cyclodextrin](1).[I3-] 5.34 N.A Hiromi Kitano 2000
[a-Cyclodextrin](1).[bisphenol F] 3.26 2.30 7.0 25.0 self-assembled monolayer Hiromi Kitano 2002
[a-Cyclodextrin](1).[bisphenol A] 3.26 2.30 7.0 25.0 self-assembled monolayer Hiromi Kitano 2002
[a-Cyclodextrin](1).[bisphenol B] 3.20 1.81 7.0 25.0 self-assembled monolayer Hiromi Kitano 2002
[a-Cyclodextrin](1).[bisphenol S] 3.92 3.20 7.0 25.0 self-assembled monolayer Hiromi Kitano 2002
[a-Cyclodextrin](1).[2-methylnaphthoate] 2.30 1.30 steady-state fluorescence measurement Francisco Mendicuti 1999
[a-Cyclodextrin](1).[2-methylnaphthoate] 2.30 1.30 25.0 steady-state fluorescence spectroscopy Wayne L. Mattice 1998
[a-Cyclodextrin](1).[Acetaminophen] 0.77 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Acetic acid] 3.80 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Acetonitrile] 0.75 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Acetylbenzoic acid] 2.95 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Acetylbenzoic acid anion] 1.78 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[N-Acetylimidazole] 0.46 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[N-Acetyl-L-leucinamide] 1.30 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Acetylnaphthalene] 1.48 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-Adamantanecarboxylic acid] 2.13 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-Adamantanecarboxylic acid anion] 2.15 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Adiphenine] 1.06 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Adipic acid] 2.51 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Adipic acid anion] 2.18 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-Aminoadamantane] 2.43 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[adamantan-1-yl-ammonium] 1.70 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Aminoaniline] 0.36 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Aminobenzoic acid] 2.02 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Aminobenzoic acid] 1.73 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Aminobenzoic acid] 3.13 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Aminobenzoic acid anion] 0.95 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Aminocinnamic acid] 2.91 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Aminophthalimide] 1.96 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Amitriptylin] 1.79 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Amobarbital] 2.15 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Amobarbital anion] 2.30 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[D-Amphetamine] 1.38 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Aniline] 0.94 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-Anilinonaphthalene-8-sulfonate anion] 0.91 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Anthracene] 1.60 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Aspirin] 1.89 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Azapropazone] 1.56 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Beclomethasone dipropionate] 2.55 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Bencyclane] 0.30 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Benzalacetone] 2.02 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Benzaldehyde] 3.39 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Benz[a]anthracene] 1.94 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Benzene] 1.50 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Benzidine] 0.48 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Benzoic acid anion] 1.58 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Benzophenone] 1.70 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Benzo[a]pyrene] 2.24 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[p-Benzoquinone] 0.83 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Benzoylbenzoic acid anion] 1.40 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Benzoyltrifluoroacetone] 1.60 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Benzyl alcohol] 1.33 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Benzylamine] 1.24 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Betamethasone] 2.35 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Betamethasone 17-valerate] 2.48 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-Bicyclo[2,2,1]heptanecarboxylic acid] 1.97 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-Bicyclo[2,2,1]heptanecarboxylic acid anion] 1.34 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-Bicyclo[2,2,2]octanecarboxylic acid] 1.48 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-Bicyclo[2,2,2]octanecarboxylic acid anion] 1.48 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Biphenyl] 1.70 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Biphenylcarboxylic acid anion] 1.77 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Bromazepam] 1.78 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Bromazepam] 1.78 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[a-Cyclodextrin](1).[Bromide anion] 0.54 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Bromine] 2.68 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Bromobenzene] 2.71 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Bromobenzoic acid] 1.60 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Bromobenzoic acid] 3.22 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Bromocinnamic acid] 3.14 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Bromocinnamic acid anion] 2.47 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Bromocinnamic acid] 4.09 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Bromocinnamic acid anion] 2.76 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Bromodiphenhydramine] 3.13 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Bromofluorobenzene] 2.40 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Bromophenol] 2.85 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Bromophenol anion] 3.09 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,2-Butanediol] 1.11 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,3-Butanediol] 4.21 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,4-Butanediol] 0.90 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-Butanol] 2.00 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-Butanol] 1.91 25.0 GC Isao Sanemasa 1999
[a-Cyclodextrin](1).[2-Butanol] 1.45 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Butyl 4-hydroxybenzoate] 2.67 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-t-Butyl-4-hydroxyphenylazobenzene-4-carboxylic acid anion] 2.22 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-s-Butyl-4-hydroxyphenylazobenzene-4-sulfonate anion] 2.90 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-t-Butyl-4-hydroxyphenylazobenzene-4-sulfonate anion] 2.92 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-t-Butyl-4-hydroxyphenylazobenzene-4-sulfonate] 3.04 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-t-Butylphenol] 1.47 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-t-Butylphenol] 1.92 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-t-Butylphenyl acetate] 2.70 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-t-Butylphenyl acetate] 2.19 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-t-Butylpyridine] 1.93 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Butyric acid] 2.13 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Butyric acid anion] 1.19 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Carbamoylproxyl] 0.52 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Carbon tetrachloride] 1.62 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-CarboxyBenzoic acid] 2.37 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-CarboxyBenzoic acid] 3.13 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Carboxy-4-hydroxyphenylazo-4-aniline anion] 4.00 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Carboxy-4-hydroxyphenylazo-4-aniline] 2.62 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Carboxy-4-hydroxyphenylazobenzene-4-sulfonate] 3.57 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Carboxy-4-hydroxyphenylazo-4-chlorobenzene anion] 3.60 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Carboxy-4-hydroxyphenylazo-3,5-dimethylbenzene anion] 3.52 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Carboxy-4-hydroxyphenylazo-4-ethoxybenzene anion] 3.61 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Carboxy-4-hydroxyphenylazo-4-methylbenzene anion] 3.11 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Carboxy-4-hydroxyphenylazo-4-n-propylbenzene anion] 3.79 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Carboxy-2-nitrophenyl acetate anion] 2.05 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Carboxy-2-nitrophenyl butanoate anion] 2.11 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Carboxy-2-nitrophenyl heptanoate anion] 2.96 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Carboxy-2-nitrophenyl hexanoate anion] 2.85 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Carboxy-2-nitrophenyl octanoate anion] 3.30 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Carboxyphenyl acetate anion] 0.98 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Carboxyphenyl acetate anion] 0.83 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Cetyltrimethylammonium] 3.05 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Chlorcyclizine] 3.08 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Chlordiazepoxide] 1.07 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Chlordiazepoxide] 1.64 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[a-Cyclodextrin](1).[Chloride anion] 0.18 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Chloroaniline] 2.40 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Chlorobenzene] 2.00 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-ChloroBenzoic acid] 1.40 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-ChloroBenzoic acid] 3.07 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-ChloroBenzoic acid anion] 1.83 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-ChloroBenzoic acid] 2.85 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-ChloroBenzoic acid anion] 2.22 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Chlorocinnamic acid] 2.75 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Chlorocinnamic acid anion] 2.45 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Chlorocinnamic acid] 3.42 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Chlorocinnamic acid anion] 2.63 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Chlorocinnamic acid] 3.67 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Chlorocinnamic acid anion] 2.46 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Chlorofluorobenzene] 1.81 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Chloroform] 1.62 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-(3-Chloro-4-hydroxyphenylazo)naphthalene-4-sulfonate anion] 2.45 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-(3-Chloro-4-hydroxyphenylazo)naphthalene-4-sulfonate] 2.66 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Chloronitrobenzene] 1.43 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Chloronitrobenzene] 1.77 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Chloronitrobenzene] 1.83 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Chlorophenol] 2.43 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Chlorophenol anion] 2.69 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Chlorophenyl acetate] 2.25 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Chlorophenyl acetate] 1.80 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Chlorpromazine] 2.08 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[trans-Cinnamic acid] 3.35 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[trans-Cinnamic acid anion] 2.04 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Cinnarizine] 1.45 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Clobazam] 1.08 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Clonazepam] 1.34 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Cortisone] 1.80 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Cortisone acetate] 1.93 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Cyanoaniline] 2.65 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-CyanoBenzoic acid anion] 0.88 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-CyanoBenzoic acid] 2.56 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-CyanoBenzoic acid anion] 1.78 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-CyanoBenzoic acid] 2.64 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-CyanoBenzoic acid anion] 1.90 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Cyanophenol] 1.98 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Cyanophenol anion] 2.68 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Cyanophenol] 2.15 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Cyanophenol anion] 2.82 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Cyclizine] 1.68 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Cyclobutane-1,1-dicarboxylatodiammine Pt (II)] 1.78 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Cyclobutanol] 1.59 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Cyclobutanol] 1.36 0.30 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[Cyclodecane] 2.26 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Cycloheptane] 1.30 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Cycloheptanol] 1.90 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Cyclohexane] 2.63 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Cyclohexanecarboxylic acid] 1.70 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Cyclohexanecarboxylic acid anion] 1.72 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[cis-1,2-Cyclohexanediol] 1.20 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[cis-1,2-Cyclohexanediol] 1.59 0.30 7.0 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[trans-1,2-Cyclohexanediol] 1.23 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[trans-1,2-Cyclohexanediol] 1.61 1.04 7.0 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[Cyclohexanol] 1.86 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Cyclohexanol] 1.70 0.90 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[Cyclohexanone] 1.34 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Cyclooctane] -0.22 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Cyclooctanol] 2.25 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Cyclopentane] 1.26 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Cyclopentanol] 1.66 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Cyclopentanol] 1.80 0.30 7.0 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[Cyclopentanol] 1.60 0.70 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[n-Decanoic acid] 3.30 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[n-Decanoic acid anion] 3.03 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[N-Desmethyldiazepam] 1.31 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Dexamethasone] 2.23 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Dexamethasone acetate] 2.50 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Diacetin] 1.11 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,4-Diacetylbenzene] 1.01 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Diazepam] 1.38 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Diazepam] 1.38 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[a-Cyclodextrin](1).[1,4-Dibromobenzene] 2.96 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4,4'-Dibromobiphenyl] 3.64 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Di-t-butylnitroxide] 0.78 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,4-Dichlorobenzene] 2.37 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4,4'-Dichlorobiphenyl] 3.01 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3,5-Dichloro-4-hydroxyphenylazobenzene-4-carboxylic acid anion] 4.86 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Dichloromethane] 1.45 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,3-Dicyanobenzene] 1.29 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,4-Dicyanobenzene] 1.52 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4,4'-Dicyanobiphenyl] 2.48 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Dicyclomine] 2.45 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,4-Diethoxybenzene] 2.11 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Diethylethylphosphonate] 1.83 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[5,5-Diethylthiobarbituric acid] 2.70 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Diflunisal anion] 1.23 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,4-Difluorobenzene] 1.29 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,4-Dihydroxybenzene] 1.38 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3,4-Dihydroxybenzoic acid] 2.85 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4,4'-Dihydroxybiphenyl] 1.61 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,4-Dihydroxybutane] 0.89 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3,4-Dihydroxycinnamic acid] 3.34 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3,4-Dihydroxycinnamic acid anion] 2.39 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,10-Dihydroxydecane] 3.85 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,7-Dihydroxyheptane] 2.50 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,6-Dihydroxyhexane] 2.01 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,9-Dihydroxynonane] 3.55 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,8-Dihydroxyoctane] 3.08 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,5-Dihydroxypentane] 1.45 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,3-Dihydroxypropane] 0.34 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,4-Diiodobenzene] 3.70 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-(3,5-Diisopropyl-4-hydroxyphenylazo)benzenesulfonate anion] 2.96 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-(3,5-Diisopropyl-4-hydroxyphenylazo)benzenesulfonate] 2.89 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,4-Dimethoxybenzene] 1.75 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3,4-Dimethoxycinnamic acid] 3.62 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3,5-Dimethoxycinnamic acid] 3.29 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Dimethylaminoazobenzene] 3.08 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Dimethylaminocinnamic acid] 3.11 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Dimethylaminocinnamic acid anion] 2.26 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Dimethylaminophenylazobenzene-4-sulfonate anion] 3.79 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4,4'-Dimethylbiphenyl] 3.00 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3,3-Dimethyl-2-butanol] 1.30 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2,5-Dimethyl-4-hydroxyphenylazobenzene-4-carboxylic acid anion] 3.09 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3,5-Dimethyl-4-hydroxyphenylazobenzene-4-carboxylic acid anion] 4.35 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-(3,5-Dimethyl-4,6-dihydroxyphenylazo)benzenesulfonate anion] 3.11 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-(3,5-Dimethyl-4,6-dihydroxyphenylazo)benzenesulfonate] 2.11 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3,5-Dimethyl-4-hydroxybenzoic acid anion] 1.25 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3,5-Dimethyl-4-hydroxycinnamic acid anion] 2.51 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3,5-Dimethyl-4-hydroxyhydrocinnamic acid anion] 1.83 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3,5-Dimethyl-4-hydroxyhydrocinnamic acid] 1.14 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-(2,3-Dimethyl-4-hydroxyphenylazo)benzenesulfonate anion] 2.89 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-(2,3-Dimethyl-4-hydroxyphenylazo)benzenesulfonate] 2.65 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-(3,5-Dimethyl-4-hydroxyphenylazo)benzenesulfonate anion] 3.75 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-(3,5-Dimethyl-4-hydroxyphenylazo)benzenesulfonate] 3.72 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,4-Dimethylnaphthalene] 1.63 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,5-Dimethylnaphthalene] 1.45 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,8-Dimethylnaphthalene] 1.30 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2,6-Dimethyl-4-nitrophenol] 2.75 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2,6-Dimethyl-4-nitrophenol anion] 3.03 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3,5-Dimethylphenol] 1.80 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3,5-Dimethylphenyl acetate] 1.82 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2,2-Dimethyl-1-propanol] 1.47 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2,2-Dimethylpropionic acid anion] 0.70 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Dimethylsulfoxide] -0.39 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,4-Dimethyl terephthalate] 2.67 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,3-Dinitrobenzene] 1.34 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,4-Dinitrobenzene] 1.55 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4,4'-Dinitrobiphenyl] 2.93 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Dioxane] 0.64 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Diphenhydramine] 1.65 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Diphenidol] 1.64 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Diphenylhydantoin] 2.04 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Diphenylpyraline] 1.50 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Dodecylammonium] 3.36 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Dodecylbenzenesulfonate anion] 3.76 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-Dodecylpyridinium] 3.45 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Dodecylsulfate anion] 3.05 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Dodecyltrimethylammonium] 3.39 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Doxepin] 1.70 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Ethanol] 0.83 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Ethyl 4-aminobenzoate] 2.27 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Ethylbenzene] 2.04 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[5-Ethyl-5-n-butylbarbituric acid] 2.63 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[5-Ethyl-5-n-butylbarbituric acid anion] 2.34 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[5-Ethyl-5-n-butylthiobarbituric acid] 2.78 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[5-Ethyl-5-n-butylthiobarbituric acid anion] 2.41 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[5-Ethyl-5-n-heptylbarbituric acid] 3.62 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[5-Ethyl-5-n-heptylbarbituric acid anion] 2.93 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[5-Ethyl-5-n-hexylbarbituric acid] 3.38 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[5-Ethyl-5-n-hexylbarbituric acid anion] 2.83 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[5-Ethyl-5-n-hexylthiobarbituric acid] 3.46 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[5-Ethyl-5-n-hexylthiobarbituric acid anion] 2.98 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Ethyl 4-hydroxybenzoate] 2.20 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Ethyl-4-hydroxyphenylazobenzene-4-carboxylic acid anion] 2.67 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-(3-Ethyl-4-hydroxyphenylazo)benzenesulfonate anion] 4.00 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-(3-Ethyl-4-hydroxyphenylazo)benzenesulfonate] 3.59 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-(3-Ethyl-4-hydroxyphenylazo)naphthalene-5-sulfonate anion] 2.34 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-(3-Ethyl-4-hydroxyphenylazo)naphthalene-5-sulfonate] 2.86 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[5-Ethyl-5-n-pentylbarbituric acid] 2.94 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[5-Ethyl-5-n-pentylbarbituric acid anion] 2.65 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[5-Ethyl-5-n-pentylthiobarbituric acid] 3.27 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[5-Ethyl-5-n-pentylthiobarbituric acid anion] 2.68 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Ethylphenyl acetate] 1.97 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[5-Ethyl-5-n-propylbarbituric acid] 2.72 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[5-Ethyl-5-n-propylbarbituric acid anion] 2.34 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[5-Ethyl-5-n-propylthiobarbituric acid] 2.88 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[5-Ethyl-5-n-propylthiobarbituric acid anion] 2.38 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Ferrocenemonocarboxylic acid anion] 2.11 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Fludiazepam] 1.43 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Fludiazepam] 1.43 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[a-Cyclodextrin](1).[Flufenamic acid] 0.78 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Flunitrazepam] 1.18 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Fluocinolone acetonide] 2.47 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Fluoride anion] 0.20 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Fluoroanisole] 1.77 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Fluorobenzene] 1.53 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-FluoroBenzoic acid] 1.50 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-FluoroBenzoic acid] 3.00 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-FluoroBenzoic acid anion] 1.15 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Fluorophenol anion] 1.19 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Flurazepam] 1.00 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Flurbiprofen] 1.30 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Flurbiprofen anion] 1.84 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Formic acid] 0.61 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[D-Fructose] 1.72 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Fumaric acid] 3.57 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Fumaric acid anion] 2.30 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[D-Galactose] 1.19 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[D-Glucose] 1.56 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[n-Heptane] 1.57 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-Heptanol] 3.07 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-Heptanol] 2.95 1.65 5.5 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Heptanol] 2.58 1.34 7.0 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Heptanol] 2.52 1.81 11.3 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Heptanol] 2.49 1.60 1.3 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Heptanol] 3.39 1.70 25.0 GC Isao Sanemasa 1999
[a-Cyclodextrin](1).[4-Heptanol] 2.27 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[n-Hexane] 1.26 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,2-Hexanediol] 2.27 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,5-Hexanediol] 1.54 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,6-Hexanediol] 1.97 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2,5-Hexanediol] 1.41 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[n-Hexanoic acid] 2.91 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[n-Hexanoic acid anion] 2.32 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-Hexanol] 2.94 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-Hexanol] 2.93 1.30 25.0 GC Isao Sanemasa 1999
[a-Cyclodextrin](1).[2-Hexanol] 2.55 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Hexanol] 2.19 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Hexobarbital] 2.34 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Hexobarbital anion] 2.34 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Hydrocinnamic acid] 3.10 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Hydrocortisone] 1.76 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Hydrocortisone acetate] 1.94 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Hydrocortisone butyrate] 2.48 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Hydroxybenzoic acid] 2.66 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Hydroxybenzoic acid anion] 0.80 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Hydroxybenzoic acid] 3.05 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Hydroxybenzoic acid anion] 1.22 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Hydroxycinnamic acid] 3.05 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Hydroxycinnamic acid] 3.12 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Hydroxycinnamic acid anion] 1.95 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Hydroxycinnamic acid] 3.30 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Hydroxycinnamic acid anion] 2.04 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Hydroxyphenylazobenzene-4-carboxylic acid anion] 4.13 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Hydroxyphenylazobenzene-4-sulfonate anion] 3.80 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Hydroxyphenylazobenzene-4-sulfonate] 3.76 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-(4-Hydroxyphenylazo)naphthalene-5-sulfonate anion] 2.59 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-(4-Hydroxyphenylazo)naphthalene-5-sulfonate] 2.32 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Hydroxypyridine] 1.55 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Hydroxyzine] 3.06 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Imidazole] 1.21 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Imipramin] 1.91 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Indole] 0.30 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Indomethacin] 2.04 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Iodide anion] 1.09 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Iodoaniline] 3.45 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Iodobenzene] 3.04 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Iodofluorobenzene] 2.99 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Iodophenol] 3.36 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Isopropylbenzene] 1.86 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Isopropyl-4-hydroxyphenylazobenzene-4-sulfonate anion] 3.65 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Isopropyl-4-hydroxyphenylazobenzene-4-sulfonate] 3.70 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Isoquinoline] 1.36 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Lauryl sulfate anion] 2.05 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Lorazepam] 1.43 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Maleic acid] 1.39 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Maleic acid anion] 1.88 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Malonic acid] 1.19 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Malonic acid anion] 1.51 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[L-Mandelic acid] 2.30 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[L-Mandelic acid anion] 0.89 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[D-Mandelic acid anion] 0.89 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[D-Mannose] 1.77 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Maprotilin] 2.09 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Meclizine] 2.94 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Medazepam] 1.66 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Medazepam] 1.66 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[a-Cyclodextrin](1).[Mephobarbital] 2.40 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Mephobarbital anion] 2.08 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Methanol] -0.05 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[L-Methionine] 0.95 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Methoxyaniline] 0.83 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Methoxybenzene] 2.43 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Methoxybenzoic acid] 1.50 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Methoxybenzoic acid anion] 0.86 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Methoxybenzoic acid] 2.93 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Methoxybenzoic acid anion] 1.17 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Methoxybenzoic acid] 2.95 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Methoxybenzoic acid anion] 0.54 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Methoxycinnamic acid] 2.75 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Methoxycinnamic acid] 3.40 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Methoxycinnamic acid anion] 1.85 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Methoxycinnamic acid] 4.01 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Methoxycinnamic acid anion] 2.44 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Methoxyphenol anion] 0.43 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Methylacetanilide] 1.23 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Methylacetanilide] 1.00 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Methylacetanilide] 1.50 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-N-Methylaminobenzoic acid] 3.11 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-N-Methylaminobenzoic acid anion] 0.79 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Methylaniline] 1.76 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Methylanisole] 1.82 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Methylbenzoic acid] 2.62 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Methylbenzoic acid] 2.82 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Methylbenzoic acid anion] 1.17 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Methylbenzoic acid] 3.04 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Methylbenzoic acid anion] 0.82 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[(-)-a-Methylbenzylamine] 1.53 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[(+)-a-Methylbenzylamine] 1.41 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Methyl-1-butanol] 2.04 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Methyl-2-butanol] 1.53 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Methyl-1-butanol] 1.87 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Methyl-2-butanol] 1.27 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Methyl trans-cinnamate] 3.08 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Methylcinnamic acid] 2.44 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Methylcinnamic acid] 3.49 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Methylcinnamic acid anion] 2.12 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Methylcinnamic acid] 4.13 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Methylcinnamic acid anion] 2.55 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Methylcyclohexanone] 1.48 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Methyl 3,4-dihydroxybenzoate] 2.65 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Methyl a-D-glucopyranoside] 1.32 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Methyl 4-hydroxybenzoate] 2.76 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Methyl-4-hydroxy-5-carboxyphenylazobenzene-4-sulfonate] 3.45 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Methyl-4-hydroxy-5-nitrophenylazobenzene-4-carboxylic acid] 2.90 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Methyl-4-hydroxyphenylazobenzene-4-carboxylic acid anion] 3.20 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Methyl-4-hydroxyphenylazobenzene-4-sulfonate anion] 3.92 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Methyl-4-hydroxyphenylazobenzene-4-sulfonate] 3.67 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-(3-Methyl-4-hydroxyphenylazo)naphthalene-4-sulfonate anion] 2.26 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-(3-Methyl-4-hydroxyphenylazo)naphthalene-4-sulfonate] 2.26 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[N-Methylimidazole] 1.13 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-Methylnaphthalene] 1.60 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Methylnaphthalene] 1.34 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Methyl-4-nitrophenol anion] 1.38 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Methyl Orange anion] 3.66 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Methyl Orange] 2.83 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Methyl Orange] 2.83 0.00 1.0 25.0 UV-vis spectroscopy Agustín G. Asuero 2006
[a-Cyclodextrin](1).[4-Methyl-2-pentanol] 1.72 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Methylphenol] 1.57 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Methylphenol anion] 2.21 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Methylphenyl acetate] 1.72 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Methylphenyl acetate] 1.77 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Methylphenyl acetate] 1.96 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Methyl-1-propanol] 1.34 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Methyl-2-propanol] 0.61 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Methylpropionic acid] 0.65 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-(2-Methyl-n-propyl)-4-hydroxyphenylazobenzene-4-sulfonate anion] 3.75 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-(2-Methyl-n-propyl)-4-hydroxyphenylazobenzene-4-sulfonate] 3.77 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Methyl Red anion] 3.96 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Methyl Red] 3.61 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Methyl 3,4,5-trihydroxybenzoate] 2.33 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Monoacetin] 0.95 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Naphthalene] 1.89 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-Naphthaleneacetic acid anion] 2.94 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Naphthalenesulfonate anion] 2.56 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2,7-Naphthalenedisulfonate] 0.98 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Naphthol] 2.10 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Naphthoyltrifluoroacetone] 1.86 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Nimetazepam] 1.38 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Nitrate anion] 0.15 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Nitrazepam] 1.41 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Nitrazine Yellow] 1.87 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Nitrazine Yellow] 1.87 0.01 9.2 25.0 UV-vis spectroscopy Agustín G. Asuero 2006
[a-Cyclodextrin](1).[2-Nitroaniline] 1.36 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Nitroaniline] 1.86 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Nitroaniline] 2.67 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Nitrobenzene] 1.69 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-NitroBenzoic acid] 1.92 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-NitroBenzoic acid anion] 0.61 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-NitroBenzoic acid] 2.04 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-NitroBenzoic acid anion] 2.69 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-NitroBenzoic acid] 2.54 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-NitroBenzoic acid anion] 2.56 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Nitrobenzyl alcohol] 0.95 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Nitrobenzyl alcohol] 1.40 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Nitrobenzyl alcohol] 1.45 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Nitrocinnamic acid] 2.01 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Nitrocinnamic acid] 2.71 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Nitrocinnamic acid] 2.76 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Nitrocinnamic acid anion] 2.42 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Nitroimidazole] 1.70 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Nitrophenol] 0.90 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Nitrophenol anion] 2.30 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Nitrophenol] 2.07 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Nitrophenol anion] 2.70 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Nitrophenol] 2.30 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Nitrophenol anion] 3.34 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Nitrophenyl acetate] 1.76 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Nitrophenyl acetate] 1.92 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Nitrophenylacetic acid] 1.69 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Nitrophenyl butyrate] 2.32 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Nitrophenyl dodecanoate] 3.43 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Nitrophenyl hexanoate] 2.70 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Nitrophenyl octanoate] 3.01 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[S-Nitroso-N-acetylpenicillamine] 1.41 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Nocloprost] 3.05 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[n-Nonane] 1.90 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-Noradamantanecarboxylic acid] 2.09 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Norbornaneacetic acid] 2.52 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Norbornaneacetic acid anion] 2.00 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[D-Norleucine] 1.66 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[L-Norleucine] 1.66 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[D-Norvaline] 1.08 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[L-Norvaline] 1.08 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[n-Octane] 1.90 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[n-Octanoic acid] 3.25 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[n-Octanoic acid anion] 2.95 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-Octanol] 3.80 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-Octanol] 3.69 1.78 25.0 GC Isao Sanemasa 1999
[a-Cyclodextrin](1).[2-Octanol] 3.15 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Orphenadrine] 1.55 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Oxalic acid] 1.40 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Oxalic acid anion] 0.38 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Oxazepam] 1.64 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Penicillin V anion] 1.72 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[n-Pentane] 0.90 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,2-Pentanediol] 1.89 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,5-Pentanediol] 1.49 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[n-Pentanoic acid] 2.73 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[n-Pentanoic acid anion] 1.88 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-Pentanol] 2.48 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-Pentanol] 2.46 0.48 25.0 GC Isao Sanemasa 1999
[a-Cyclodextrin](1).[2-Pentanol] 2.13 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Pentanol] 2.06 25.0 GC Isao Sanemasa 1999
[a-Cyclodextrin](1).[3-Pentanol] 1.94 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Pentobarbital] 2.61 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Pentobarbital anion] 2.04 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Perchlorate anion] 1.46 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Perfluorobutyric acid anion] 1.46 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Perfluoroheptanoic acid anion] 1.41 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Perfluorononanoic acid anion] 1.36 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Perfluorooctanoic acid anion] 1.45 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Phenanthrene] 1.20 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Phenethylamine] 1.42 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Pheniramine] 1.83 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Phenobarbital] 2.23 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Phenobarbital anion] 2.08 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Phenol] 1.57 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Phenol anion] 1.04 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Phenolphthalein] 2.73 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Phenol Red anion] 2.62 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Phenol Red] 0.73 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Phenyl acetate] 1.66 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[L-Phenylalanine anion] 1.09 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[L-Phenylalanine methyl ester] 1.28 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Phenylbutazone] 2.85 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Pimelic acid] 2.87 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Prednisolone] 2.47 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Prednisolone acetate] 2.44 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Proadifen] 2.26 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Progesterone] 2.16 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,2-Propanediol] 0.48 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,3-Propanediol] 0.63 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-Propanol] 1.43 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2-Propanol] 0.66 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Propionic acid] 1.58 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Propionic acid anion] 0.26 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[n-Propylbenzene] 2.77 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Propyl 4-hydroxybenzoate] 2.22 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-n-Propyl-4-hydroxyphenylazobenzene-4-sulfonate anion] 3.92 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3-n-Propyl-4-hydroxyphenylazobenzene-4-sulfonate] 3.53 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-(3-n-Propyl-4-hydroxyphenylazo)naphthalene-5-sulfonate anion] 2.51 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1-(3-n-Propyl-4-hydroxyphenylazo)naphthalene-5-sulfonate] 2.51 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Prostaglandin B1] 2.16 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Prostaglandin B2] 1.98 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Prostaglandin F2a] 2.26 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Prostaglandin F2a anion] 1.33 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Pyrene] 1.43 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Pyridine] 2.20 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Quinoline] 1.46 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Salicylic acid] 1.51 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Salicylic acid anion] 0.89 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Sorbic acid] 2.81 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Suberic acid] 3.15 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Suberic acid anion] 2.99 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Succinic acid] 2.01 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Succinic acid anion] 1.25 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Sulfate] -0.05 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Testosterone] 2.13 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Tetradecyltrimethylammonium] 3.65 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Thiocyanate anion] 2.36 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Thiopental] 2.45 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Thiopental anion] 2.36 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Thiophenobarbital] 3.52 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Toluene] 1.52 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[4-Toluenesulfonate anion] 1.22 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[6-p-Toluidinylnaphthalene-2-sulfonate anion] 1.62 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Triacetin] 1.08 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Triamcinolone] 2.08 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Triamcinolone acetonide] 2.41 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Triamcinolone diacetate] 2.48 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[D-N-Trifluoroacetyl-4-fluorophenylalanine anion] 1.06 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[L-N-Trifluoroacetyl-4-fluorophenylalanine anion] 1.06 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[D-N-Trifluoroacetylphenylalanine anion] 0.79 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[L-N-Trifluoroacetylphenylalanine anion] 0.80 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[3,4,5-Trihydroxybenzoic acid] 2.33 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Trimethylacetic acid] 1.18 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,2,3-Trimethylbenzene] 1.11 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,2,4-Trimethylbenzene] 1.66 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[1,3,5-Trimethylbenzene] 1.79 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[2,3,5-Trimethyl-4-hydroxyphenylazobenzene-4-carboxylic acid anion] 3.10 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Triprolidine] 1.75 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[d-Valerolactam] 0.70 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[Vanillin] 1.19 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[o-Xylene] 1.20 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[m-Xylene] 1.60 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[p-Xylene] 1.75 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[D-Xylose] 1.57 25.0 Kenneth A. Connors 1995
[a-Cyclodextrin](1).[chiral N-imidazole derivative 1 (R enantiomer)] 1.57 25.0 NMR spectroscopy Claude Vaccher 2006
[a-Cyclodextrin](1).[chiral N-imidazole derivative 1 (S enantiomer)] 1.00 26.0 NMR spectroscopy Claude Vaccher 2006
[a-Cyclodextrin](1).[4-tert-butylcatechol] 1.67 1.48 25.0 NMR spectroscopy Dona1 H. Macartney 1993
[a-Cyclodextrin](1).[4-tert-butylcatechol] 2.15 25.0 UV-vis spectroscopy Dona1 H. Macartney 1993
[a-Cyclodextrin](2).[4-tert-butylcatechol] 1.46 0.90 25.0 NMR spectroscopy Dona1 H. Macartney 1993
[a-Cyclodextrin](2).[4-tert-butylcatechol] 0.70 25.0 UV-vis spectroscopy Dona1 H. Macartney 1993
[a-Cyclodextrin](1).[1,1'-(a,w-octanediyl)bis(pyrazinium) diiodid] 1.23 0.30 7.0 25.0 NMR spectroscopy Donald H. Macartney 1994
[a-Cyclodextrin](1).[1,1'-(a,w-nonanediyl)bis(pyrazinium) diiodid] 2.11 1.85 7.0 25.0 NMR spectroscopy Donald H. Macartney 1994
[a-Cyclodextrin](1).[1,1'-(a,w-decanediyl)bis(pyrazinium) diiodid] 3.04 2.00 7.0 25.0 NMR spectroscopy Donald H. Macartney 1994
[a-Cyclodextrin](1).[1,1'-(a,w-undecanediyl)bis(pyrazinium) diiodid] 3.43 2.48 7.0 25.0 NMR spectroscopy Donald H. Macartney 1994
[a-Cyclodextrin](1).[1,1'-(a,w-dodecanediyl)bis(pyrazinium) diiodid] 3.51 2.87 7.0 25.0 NMR spectroscopy Donald H. Macartney 1994
[a-Cyclodextrin](1).[(a,w-octanediyl)-l-(4,4'-bipyridinium)-1"-(pyrazinium) diodide] 1.62 0.48 7.0 25.0 NMR spectroscopy Donald H. Macartney 1994
[a-Cyclodextrin](1).[(a,w-nonanediyl)-l-(4,4'-bipyridinium)-1"-(pyrazinium) diodide] 2.34 1.48 7.0 25.0 NMR spectroscopy Donald H. Macartney 1994
[a-Cyclodextrin](1).[(a,w-decnediyl)-l-(4,4'-bipyridinium)-1"-(pyrazinium) diodide] 3.15 2.11 7.0 25.0 NMR spectroscopy Donald H. Macartney 1994
[a-Cyclodextrin](1).[(a,w-undecanediyl)-l-(4,4'-bipyridinium)-1"-(pyrazinium) diodide] 3.45 2.52 7.0 25.0 NMR spectroscopy Donald H. Macartney 1994
[a-Cyclodextrin](1).[(a,w-dodecanediyl)-l-(4,4'-bipyridinium)-1"-(pyrazinium) diodide] 3.62 2.48 7.0 25.0 NMR spectroscopy Donald H. Macartney 1994
[a-Cyclodextrin](1).[1,l"-(a,w-octanediyl)bis(4,4'-bipyridinium) dication] 1.86 0.30 7.0 25.0 NMR spectroscopy Donald H. Macartney 1994
[a-Cyclodextrin](1).[1,l"-(a,w-nonanediyl)bis(4,4'-bipyridinium) dication] 2.64 1.48 7.0 25.0 NMR spectroscopy Donald H. Macartney 1994
[a-Cyclodextrin](1).[1,l"-(a,w-decanediyl)bis(4,4'-bipyridinium) dication] 3.18 2.00 7.0 25.0 NMR spectroscopy Donald H. Macartney 1994
[a-Cyclodextrin](1).[1,l"-(a,w-undecanediyl)bis(4,4'-bipyridinium) dication] 3.53 2.60 7.0 25.0 NMR spectroscopy Donald H. Macartney 1994
[a-Cyclodextrin](1).[1,l"-(a,w-dodecanediyl)bis(4,4'-bipyridinium) dication] 3.57 2.70 7.0 25.0 NMR spectroscopy Donald H. Macartney 1994
[a-Cyclodextrin](2).[phenylbutazone] 3.20 2.00 7.5 15.0 UV-vis spectroscopy David Diaz 1998
[a-Cyclodextrin](2).[phenylbutazone] 3.32 2.70 7.5 20.0 UV-vis spectroscopy David Diaz 1998
[a-Cyclodextrin](2).[phenylbutazone] 3.60 2.78 7.5 25.0 UV-vis spectroscopy David Diaz 1998
[a-Cyclodextrin](2).[phenylbutazone] 3.78 3.00 7.5 30.0 UV-vis spectroscopy David Diaz 1998
[a-Cyclodextrin](2).[phenylbutazone] 3.90 3.00 7.5 37.0 UV-vis spectroscopy David Diaz 1998
[a-Cyclodextrin](1).[phenylbutazone] 3.85 3.30 15.0 UV-vis spectroscopy David Diaz 1998
[a-Cyclodextrin](1).[phenylbutazone] 3.65 2.90 20.0 UV-vis spectroscopy David Diaz 1998
[a-Cyclodextrin](1).[phenylbutazone] 3.79 2.95 25.0 UV-vis spectroscopy David Diaz 1998
[a-Cyclodextrin](1).[phenylbutazone] 3.72 2.95 30.0 UV-vis spectroscopy David Diaz 1998
[a-Cyclodextrin](1).[phenylbutazone] 3.67 2.90 37.0 UV-vis spectroscopy David Diaz 1998
[a-Cyclodextrin](2).[oxyphenbutazone] 3.62 2.30 7.5 15.0 UV-vis spectroscopy David Diaz 1998
[a-Cyclodextrin](2).[oxyphenbutazone] 3.04 1.60 7.5 20.0 UV-vis spectroscopy David Diaz 1998
[a-Cyclodextrin](2).[oxyphenbutazone] 2.98 1.85 7.5 25.0 UV-vis spectroscopy David Diaz 1998
[a-Cyclodextrin](2).[oxyphenbutazone] 2.60 1.30 7.5 30.0 UV-vis spectroscopy David Diaz 1998
[a-Cyclodextrin](2).[oxyphenbutazone] 2.04 0.85 7.5 37.0 UV-vis spectroscopy David Diaz 1998
[a-Cyclodextrin](1).[oxyphenbutazone] 2.71 1.85 15.0 UV-vis spectroscopy David Diaz 1998
[a-Cyclodextrin](1).[oxyphenbutazone] 3.00 2.48 20.0 UV-vis spectroscopy David Diaz 1998
[a-Cyclodextrin](1).[oxyphenbutazone] 2.71 1.78 25.0 UV-vis spectroscopy David Diaz 1998
[a-Cyclodextrin](1).[oxyphenbutazone] 2.85 2.30 30.0 UV-vis spectroscopy David Diaz 1998
[a-Cyclodextrin](1).[oxyphenbutazone] 2.85 2.00 37.0 UV-vis spectroscopy David Diaz 1998
[a-Cyclodextrin](1).[sodium a,w-hexyl dicarboxylate] 2.48 2.18 10.5 25.0 Apparent molar volume measurements Ronald E. Verrall 2000
[a-Cyclodextrin](1).[sodium a,w-hexyl dicarboxylate] 2.21 0.48 Ronald E. Verrall 2000
[a-Cyclodextrin](1).[sodium a,w-octyl dicarboxylate] 2.79 2.20 10.5 25.0 Apparent molar volume measurements Ronald E. Verrall 2000
[a-Cyclodextrin](1).[sodium a,w-octyl dicarboxylate] 3.18 1.36 Ronald E. Verrall 2000
[a-Cyclodextrin](1).[sodium a,w-decanyl dicarboxylate] 3.30 3.00 10.5 25.0 Apparent molar volume measurements Ronald E. Verrall 2000
[a-Cyclodextrin](2).[sodium a,w-decanyl dicarboxylate] 2.70 2.40 10.5 25.0 Apparent molar volume measurements Ronald E. Verrall 2000
[a-Cyclodextrin](1).[sodium a,w-dodecyl dicarboxylate] 3.70 3.40 10.5 25.0 Apparent molar volume measurements Ronald E. Verrall 2000
[a-Cyclodextrin](2).[sodium a,w-dodecyl dicarboxylate] 3.85 2.54 10.5 25.0 Apparent molar volume measurements Ronald E. Verrall 2000
[a-Cyclodextrin](1).[trans-1,2-bis(4-pyridyl)ethylene] 1.52 0.30 7.0 25.0 UV-vis spectroscopy Donal H. Macartney 2000
[a-Cyclodextrin](1).[trans-1,2-bis(4-pyridyl)ethylene] 1.71 0.30 7.0 25.0 NMR spectroscopy Donal H. Macartney 2000
[a-Cyclodextrin](1).[4,4'-azopyridine ligand] 2.47 1.56 7.0 25.0 UV-vis spectroscopy Donal H. Macartney 2000
[a-Cyclodextrin](1).[4,4'-azopyridine ligand] 2.44 0.70 7.0 25.0 NMR spectroscopy Donal H. Macartney 2000
[a-Cyclodextrin](1).[4-pyridinecarboxaldehyde azine] 3.32 2.40 7.0 25.0 UV-vis spectroscopy Donal H. Macartney 2000
[a-Cyclodextrin](2).[4-pyridinecarboxaldehyde azine] 1.85 1.30 7.0 25.0 UV-vis spectroscopy Donal H. Macartney 2000
[a-Cyclodextrin](1).[4-acetylpyridine azine] 1.43 0.90 7.0 25.0 UV-vis spectroscopy Donal H. Macartney 2000
[a-Cyclodextrin](1).[4-acetylpyridine azine] 1.32 1.00 7.0 25.0 NMR spectroscopy Donal H. Macartney 2000
[a-Cyclodextrin](2).[4-acetylpyridine azine] 0.78 0.30 7.0 25.0 UV-vis spectroscopy Donal H. Macartney 2000
[a-Cyclodextrin](2).[4-acetylpyridine azine] 0.60 0.30 7.0 25.0 NMR spectroscopy Donal H. Macartney 2000
[a-Cyclodextrin](1).[[(NC)5Fe(bpe)Fe(CN)5]6-] 1.85 1.20 7.0 25.0 UV-vis spectroscopy Donal H. Macartney 2000
[a-Cyclodextrin](1).[[(NC)5Fe(azp)Fe(CN)5]6-] 3.11 1.90 7.0 25.0 UV-vis spectroscopy Donal H. Macartney 2000
[a-Cyclodextrin](1).[[(NC)5Fe(pca)Fe(CN)5]6-] 2.88 2.11 7.0 25.0 UV-vis spectroscopy Donal H. Macartney 2000
[a-Cyclodextrin](1).[20(S)-Camptothecin] 2.27 1.7 25.0 HPLC-method Vijay Kumar 2002
[a-Cyclodextrin](1).[propanol] 1.33 -0.82 7.0 25.0 NMR spectroscopy Noriaki Funasaki 2002
[a-Cyclodextrin](1).[propanesulfonate] 1.36 0.10 7.0 25.0 NMR spectroscopy Noriaki Funasaki 2002
[a-Cyclodextrin](1).[1-butanol] 1.87 7.0 25.0 Modified static head-space gas chromatography method Yoshihiro Saito 2004
[a-Cyclodextrin](1).[1-butanol] 1.95 Spectrophotometry Yoshihiro Saito 2004
[a-Cyclodextrin](1).[1-butanol] 1.97 Surface tension Yoshihiro Saito 2004
[a-Cyclodextrin](1).[1-butanol] 1.97 1.30 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[1-butanol] 1.90 0.40 6.9 25.0 Titration calorimetry Robert N. Goldberg 1994
[a-Cyclodextrin](1).[1-pentanol ] 2.46 7.0 25.0 Modified static head-space gas chromatography method Yoshihiro Saito 2004
[a-Cyclodextrin](1).[1-pentanol ] 2.51 Spectrophotometry Yoshihiro Saito 2004
[a-Cyclodextrin](1).[1-pentanol ] 2.58 Surface tension Yoshihiro Saito 2004
[a-Cyclodextrin](1).[1-pentanol ] 2.46 0.60 7.0 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[a-Cyclodextrin](1).[1-hexanol] 2.97 7.0 25.0 Modified static head-space gas chromatography method Yoshihiro Saito 2004
[a-Cyclodextrin](1).[1-hexanol] 2.95 Spectrophotometry Yoshihiro Saito 2004
[a-Cyclodextrin](1).[1-hexanol] 2.84 Surface tension Yoshihiro Saito 2004
[a-Cyclodextrin](1).[1-hexanol] 2.84 1.26 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[1-hexanol] 4.95 6.4 20.0 electrochemical masurements, cyclic voltammetry Marcin Majda 2000
[a-Cyclodextrin](1).[1-hexanol] 2.95 spectrophotometry Marcin Majda 2000
[a-Cyclodextrin](1).[1-heptanol ] 3.17 7.0 25.0 Modified static head-space gas chromatography method Yoshihiro Saito 2004
[a-Cyclodextrin](1).[1-heptanol ] 3.36 Spectrophotometry Yoshihiro Saito 2004
[a-Cyclodextrin](1).[1-heptanol ] 3.10 Surface tension Yoshihiro Saito 2004
[a-Cyclodextrin](1).[1-octanol] 3.40 7.0 25.0 Modified static head-space gas chromatography method Yoshihiro Saito 2004
[a-Cyclodextrin](1).[1-octanol] 3.80 Spectrophotometry Yoshihiro Saito 2004
[a-Cyclodextrin](1).[1-octanol] 3.52 Surface tension Yoshihiro Saito 2004
[a-Cyclodextrin](1).[1-octanol] 3.52 1.88 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[3-hydroxyflavone] 1.21 7.0 25.0 UV-vis spectroscopy S. Tommasini 2004
[a-Cyclodextrin](1).[morin] 1.69 7.0 25.0 UV-vis spectroscopy S. Tommasini 2004
[a-Cyclodextrin](1).[quercetin] 1.28 7.0 25.0 UV-vis spectroscopy S. Tommasini 2004
[a-Cyclodextrin](1).[Bis( 2-pyridylcarbinolato)copper(II)] 2.53 7.0 ESR spectroscopy Hiroshi Yokoi 1991
[a-Cyclodextrin](1).[alprostadil] 2.98 2.11 7.0 27.0 NMR spectroscopy Tore Ramstad 2005
[a-Cyclodextrin](1).[alprostadil] 2.85 1.81 7.2 27.0 Capillary electrophoresis Tore Ramstad 2005
[a-Cyclodextrin](1).[alprostadil] 2.81 1.71 7.2 30.0 Capillary electrophoresis Tore Ramstad 2005
[a-Cyclodextrin](1).[alprostadil] 2.73 1.43 7.2 37.0 Capillary electrophoresis Tore Ramstad 2005
[a-Cyclodextrin](1).[1,4-methoxybenzene] 1.75 0.66 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1984
[a-Cyclodextrin](2).[1,4-methoxybenzene] 2.29 1.59 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1984
[a-Cyclodextrin](1).[1,4-ethoxybenzene] 2.11 1.20 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1984
[a-Cyclodextrin](2).[1,4-ethoxybenzene] 2.51 1.69 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1984
[a-Cyclodextrin](1).[1,4-diiodobenzene] 3.70 2.97 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1984
[a-Cyclodextrin](2).[1,4-diiodobenzene] 3.80 3.10 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1984
[a-Cyclodextrin](1).[1,4-dibromobenzene] 2.96 1.34 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1984
[a-Cyclodextrin](2).[1,4-dibromobenzene] 2.60 1.15 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1984
[a-Cyclodextrin](1).[1,4-dichlorobenzene] 2.37 1.20 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1984
[a-Cyclodextrin](2).[1,4-dichlorobenzene] 1.95 1.08 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1984
[a-Cyclodextrin](1).[terephthalic acid] 3.13 1.23 1.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1984
[a-Cyclodextrin](2).[terephthalic acid] 1.38 -0.22 1.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1984
[a-Cyclodextrin](1).[dimethyl terephthalate] 2.67 0.90 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1984
[a-Cyclodextrin](1).[dimethyl terephthalate] 2.58 25.0 fluorescence spectroscopy Francisco Mendicuti 2004
[a-Cyclodextrin](1).[dimethyl terephthalate] 2.98 1.61 5.0 fluorescence spectroscopy Francisco Mendicuti 2004
[a-Cyclodextrin](1).[dimethyl terephthalate] 2.81 1.43 15.0 fluorescence spectroscopy Francisco Mendicuti 2004
[a-Cyclodextrin](1).[dimethyl terephthalate] 2.46 1.04 35.0 fluorescence spectroscopy Francisco Mendicuti 2004
[a-Cyclodextrin](1).[dimethyl terephthalate] 2.50 1.62 45.0 fluorescence spectroscopy Francisco Mendicuti 2004
[a-Cyclodextrin](2).[dimethyl terephthalate] 2.04 0.67 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1984
[a-Cyclodextrin](1).[1,4-diacetyl benzene] 1.01 -0.15 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1984
[a-Cyclodextrin](1).[chlorpheniramine] 1.48 7.0 20.0 NMR spectroscopy Thomas J. Wenzel 2006
[a-Cyclodextrin](1).[1,4-dinitrile benzene] 1.52 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1984
[a-Cyclodextrin](2).[1,4-dinitrile benzene] 0.86 -0.15 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1984
[a-Cyclodextrin](1).[1,4-dinitrobenzene] 1.55 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1984
[a-Cyclodextrin](2).[1,4-dinitrobenzene] 0.66 -0.40 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1984
[a-Cyclodextrin](1).[pyrene] 2.83 7.0 25.0 Fluorescence spectroscopy J. N. Demas 1993
[a-Cyclodextrin](1).[brompheniramine] 1.48 7.0 20.0 NMR spectroscopy Thomas J. Wenzel 2006
[a-Cyclodextrin](1).[t-BuOH] 0.62 -0.46 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[a-Cyclodextrin](1).[neo-PenOH] 1.41 0.52 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[a-Cyclodextrin](1).[n-BuSO3-] 1.66 0.32 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[a-Cyclodextrin](1).[n-PenSO3-] 2.19 0.39 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[a-Cyclodextrin](1).[n-HexSO3-] 2.70 1.40 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[a-Cyclodextrin](1).[n-HepSO3-] 2.99 1.67 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[a-Cyclodextrin](1).[n-OctSO3-] 3.48 2.26 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[a-Cyclodextrin](1).[n-DecSO3-] 4.30 3.83 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[a-Cyclodextrin](1).[p-tolSO3-] 1.23 0.60 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[a-Cyclodextrin](1).[EtCO2-] 0.22 -1.78 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[a-Cyclodextrin](1).[n-PrCO2-] 1.05 -0.12 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[a-Cyclodextrin](1).[n-BuCO2-] 1.80 0.59 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[a-Cyclodextrin](1).[n-PenCO2-] 2.41 0.82 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[a-Cyclodextrin](1).[c-HexCO2-] 2.51 2.19 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[a-Cyclodextrin](1).[n-HexCO2-] 0.97 0.20 11.6 25.0 UV-vis spectroscopy Oswald S. Tee 1993
[a-Cyclodextrin](1).[2-naphthalenesul fonate] 2.56 0.01 7.2 25.0 Calorimetry Yoshihisa Inoue 1993
[a-Cyclodextrin](1).[2,7-naphthalenedisulfonate ] 0.98 0.06 7.2 25.0 Calorimetry Yoshihisa Inoue 1993
[a-Cyclodextrin](1).[1-naphthaleneacetate] 2.94 0.04 7.2 25.0 Calorimetry Yoshihisa Inoue 1993
[a-Cyclodextrin](1).[p-nitrophenyl a-D-mannose] 2.28 7.0 30.0 NMR spectroscopy Soledad Penades 1993
[a-Cyclodextrin](1).[p-nitrophenyl b-D-mannose] 2.52 7.0 30.0 NMR spectroscopy Soledad Penades 1993
[a-Cyclodextrin](1).[risperidone] 1.38 10.5 25.0 UV-Vis spectroscopy M.B. Zughul 2005
[a-Cyclodextrin](1).[p-nitrophenolate] 2.52 13.5 20.0 Pulse Voltammetry Janet G. Osteryoung 1991
[a-Cyclodextrin](1).[p-nitrophenolate] 2.26 13.5 25.0 UV-vis spectroscopy Janet G. Osteryoung 1991
[a-Cyclodextrin](1).[p-nitrophenolate] 3.30 2.30 11.0 24.5 Gradient flow injection spectrophotometric technique Michael A. Koupparis 1995
[a-Cyclodextrin](1).[sym-4,4'-dihydroxy biphenyl] 1.61 0.70 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1988
[a-Cyclodextrin](2).[sym-4,4'-dihydroxy biphenyl] 2.54 1.68 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1988
[a-Cyclodextrin](1).[sym-4,4'-dimethyl biphenyl] 3.00 2.24 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1988
[a-Cyclodextrin](2).[sym-4,4'-dimethyl biphenyl] 2.09 1.26 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1988
[a-Cyclodextrin](1).[biphenyl] 1.70 0.48 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1988
[a-Cyclodextrin](2).[biphenyl] 1.80 0.48 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1988
[a-Cyclodextrin](1).[sym-4,4'-dichlor biphenyl] 3.01 2.60 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1988
[a-Cyclodextrin](2).[sym-4,4'-dichlor biphenyl] 3.21 2.74 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1988
[a-Cyclodextrin](1).[sym-4,4'-dibrome biphenyl] 3.64 3.16 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1988
[a-Cyclodextrin](2).[sym-4,4'-dibrome biphenyl] 3.73 3.19 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1988
[a-Cyclodextrin](1).[sym-4,4'-diciano biphenyl] 2.48 1.23 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1988
[a-Cyclodextrin](2).[sym-4,4'-diciano biphenyl] 1.77 1.11 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1988
[a-Cyclodextrin](1).[sym-4,4'-dinitro biphenyl] 2.93 2.01 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1988
[a-Cyclodextrin](2).[sym-4,4'-dinitro biphenyl] 2.17 1.23 7.0 25.0 UV-vis spectroscopy Kenneth A. Connors 1988
[a-Cyclodextrin](1).[9-methylanthracene] 2.08 1.30 25.0 Fluorescence spectroscopy Vincent C. Reinsborough 1995
[a-Cyclodextrin](2).[manganese(III) tetrakis(4-sulfonatopheny1)porphine] 0.43 7.0 25.0 UV-vis spectroscopy Robert G. Bryant 1995
[a-Cyclodextrin](1).[p-(N,N-diethylamino)benzoic acid] 3.57 1.40 5.0 UV-vis spectroscopy Minjoong Yoon 1996
[a-Cyclodextrin](1).[2-[ (p-amino)phenyl]-3,3-dimethyl-5-cyano-3H-indole] 1.32 9.5 25.0 Fluorescence spectroscopy Gilles Durocher 1997
[a-Cyclodextrin](2).[2-[ (p-amino)phenyl]-3,3-dimethyl-5-cyano-3H-indole] 1.41 9.5 25.0 Fluorescence spectroscopy Gilles Durocher 1997
[a-Cyclodextrin](1).[2-[ (p-dimethylamino)phenyll-3,3-dimethyl-5-cyano-3H-indole] 1.23 9.5 25.0 Fluorescence spectroscopy Gilles Durocher 1997
[a-Cyclodextrin](2).[2-[ (p-dimethylamino)phenyll-3,3-dimethyl-5-cyano-3H-indole] 1.23 9.5 25.0 Fluorescence spectroscopy Gilles Durocher 1997
[a-Cyclodextrin](1).[Heptanedioic acid] 1.38 11.3 25.0 Calorimetry Giuseppina Castronuovo 1997
[a-Cyclodextrin](1).[Octanedioic acid] 1.97 0.48 11.3 25.0 Calorimetry Giuseppina Castronuovo 1997
[a-Cyclodextrin](1).[Octanedioic acid] 2.46 0.90 1.3 25.0 Calorimetry Giuseppina Castronuovo 1997
[a-Cyclodextrin](1).[Nonanedioic acid] 2.80 1.32 11.3 25.0 Calorimetry Giuseppina Castronuovo 1997
[a-Cyclodextrin](1).[Nonanedioic acid] 2.64 0.90 1.3 25.0 Calorimetry Giuseppina Castronuovo 1997
[a-Cyclodextrin](1).[Decanedioic acid ] 3.25 1.92 11.3 25.0 Calorimetry Giuseppina Castronuovo 1997
[a-Cyclodextrin](1).[Undecanedioic acid] 3.20 2.41 11.3 25.0 Calorimetry Giuseppina Castronuovo 1997
[a-Cyclodextrin](1).[Pentanedioic acid] 2.41 1.04 1.3 25.0 Calorimetry Giuseppina Castronuovo 1997
[a-Cyclodextrin](1).[Hexanedioic acid ] 2.45 0.70 1.3 25.0 Calorimetry Giuseppina Castronuovo 1997
[a-Cyclodextrin](1).[Heptanedioic acid ] 2.86 0.70 1.3 25.0 Calorimetry Giuseppina Castronuovo 1997
[a-Cyclodextrin](1).[Decanedioic acid] 3.36 2.43 1.3 25.0 Calorimetry Giuseppina Castronuovo 1997
[a-Cyclodextrin](1).[1-ethanol] 0.83 7.0 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[1-propanol] 1.43 7.0 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[1-propanol] 1.97 0.70 11.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[1-propanol] 2.17 1.11 1.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[1-butanol ] 2.00 7.0 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[1-butanol ] 2.04 0.48 11.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[1-butanol ] 2.27 0.85 1.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[1-pentanol] 2.44 1.18 7.0 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[1-pentanol] 2.58 1.04 11.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[1-pentanol] 2.75 1.04 1.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[1-pentanol] 2.58 1.40 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[1-hexanol ] 3.12 1.00 7.0 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[1-hexanol ] 3.07 1.98 11.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[1-hexanol ] 2.92 1.76 1.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[1-hexanol ] 2.92 1.48 7.0 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[a-Cyclodextrin](1).[1-heptanol] 2.89 1.63 7.0 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[1-heptanol] 2.67 1.86 11.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[1-heptanol] 2.60 1.69 1.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[1-heptanol] 3.10 1.54 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[1-octanol ] 2.64 1.72 7.0 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[1-octanol ] 3.12 1.53 11.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[1-octanol ] 2.82 1.79 1.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[1-nonanol ] 2.87 1.83 7.0 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[propanoic acid] 1.74 1.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[butanoic acid ] 2.25 0.90 1.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[butanoic acid ] 1.93 1.15 11.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[pentanoic acid] 2.78 1.41 1.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[pentanoic acid] 2.16 0.85 11.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[pentanoic acid] 5.16 3.85 11.3 25.0 calorimetry Giuseppina Castronuovo 1996
[a-Cyclodextrin](1).[hexanoic acid] 2.96 1.41 1.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[hexanoic acid] 2.71 1.73 11.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[hexanoic acid] 5.71 4.73 11.3 25.0 calorimetry Giuseppina Castronuovo 1996
[a-Cyclodextrin](1).[heptanoic acid] 2.77 1.62 1.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[heptanoic acid] 3.09 1.83 11.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[heptanoic acid] 6.09 4.83 11.3 25.0 calorimetry Giuseppina Castronuovo 1996
[a-Cyclodextrin](1).[octanoic acid] 3.13 2.04 1.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[octanoic acid] 3.13 2.05 11.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[nonanoic acid] 2.99 1.68 1.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[nonanoic acid] 2.40 1.30 11.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[decanoic acid] 2.40 0.78 11.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[undecanedioic acid] 2.93 1.23 11.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[dodecanoic acid] 3.03 2.27 11.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[dodecanoic acid] 6.03 5.27 11.3 25.0 calorimetry Giuseppina Castronuovo 1996
[a-Cyclodextrin](1).[c-pentanol ] 2.11 0.70 7.0 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[c-hexanol ] 2.20 0.95 7.0 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[c-heptanol ] 1.58 0.48 7.0 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[c-octanol] 1.58 0.85 7.0 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[propane-1,3-diol] 0.63 7.0 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[butane-1,4-diol] 0.90 7.0 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[pentane-1,5-diol] 1.49 7.0 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[pentane-1,5-diol] 2.15 0.30 11.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[hexane-1,6-diol] 1.97 7.0 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[hexane-1,6-diol] 2.51 0.78 11.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[heptane-1,7-diol ] 2.44 0.70 7.0 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[heptane-1,7-diol ] 3.00 0.85 11.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[octane-1,8-diol ] 3.28 2.39 7.0 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[octane-1,8-diol ] 3.23 1.94 11.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[nonane-1,9-diol ] 3.19 1.98 7.0 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[nonane-1,9-diol ] 3.30 2.13 11.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[decane-1,10-diol] 3.19 2.53 7.0 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[decane-1,10-diol] 3.16 2.68 11.3 25.0 Calorimetry Giuseppina Castronuovo 1998
[a-Cyclodextrin](1).[chlorpromazine hydrochloride] 2.04 7.4 37.0 Surface tension Noriaki Funasaki 1999
[a-Cyclodextrin](1).[chlorpromazine hydrochloride] 2.30 25.0 UV-vis spectroscopy Noriaki Funasaki 1999
[a-Cyclodextrin](1).[propantheline bromide] 1.90 37.0 Surface tension Noriaki Funasaki 1999
[a-Cyclodextrin](1).[TX100] 2.44 5.0 25.0 Calorimetric titrations H.-J. Buschmann 2000
[a-Cyclodextrin](1).[Benzyl tert-butyl nitroxide] 1.16 7.0 21.0 EPR spectroscopy Marco Lucarini 2004
[a-Cyclodextrin](1).[NP10 ] 2.46 5.0 25.0 Calorimetric titrations H.-J. Buschmann 2000
[a-Cyclodextrin](1).[NP20 ] 2.56 5.0 25.0 Calorimetric titrations H.-J. Buschmann 2000
[a-Cyclodextrin](1).[Igepal CO-720 ] 3.71 5.0 25.0 Calorimetric titrations H.-J. Buschmann 2000
[a-Cyclodextrin](1).[Brij56 ] 5.00 5.0 25.0 Calorimetric titrations H.-J. Buschmann 2000
[a-Cyclodextrin](1).[Brij99 ] 5.00 5.0 25.0 Calorimetric titrations H.-J. Buschmann 2000
[a-Cyclodextrin](1).[PEG1000 ] 2.51 5.0 25.0 Calorimetric titrations H.-J. Buschmann 2000
[a-Cyclodextrin](1).[cis-1,2-Cyclopentanediol ] 1.92 0.85 7.0 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[trans-1,2-Cyclopentanediol] 1.84 1.20 7.0 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[trans-1,2-Cyclopentanediol] 4.43 5.0 25.0 Calorimetric titrations H.-J. Buschmann 2000
[a-Cyclodextrin](1).[cis-1,2-Cyclooctanediol] 1.91 0.90 7.0 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[Cyclohexanol ] 1.92 0.60 7.0 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[Cycloheptanol ] 1.40 1.15 7.0 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[Cyclooctanol ] 1.45 1.28 7.0 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Cyclohexylethanol ] 1.93 0.85 7.0 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[4-Cyclohexylbutan-1-ol ] 2.99 2.20 7.0 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Butanol ] 0.95 1.04 5.5 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Butanol ] 2.00 7.0 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Butanol ] 2.04 0.48 11.3 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Butanol ] 1.97 0.60 1.3 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Pentanol ] 2.56 0.70 5.5 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Pentanol ] 2.44 1.18 7.0 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Pentanol ] 2.58 1.04 11.3 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Pentanol ] 2.50 0.78 1.3 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Hexanol ] 2.90 1.49 5.5 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Hexanol ] 2.72 0.85 7.0 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Hexanol ] 2.83 1.76 11.3 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Hexanol ] 2.64 1.34 1.3 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Octanol ] 2.94 1.69 5.5 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Octanol ] 2.34 1.43 7.0 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Octanol ] 2.29 1.52 11.3 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Octanol ] 2.62 1.60 1.3 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Nonanol] 3.02 2.36 5.5 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Nonanol] 2.68 1.57 7.0 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Nonanol] 4.13 2.00 25.0 GC Isao Sanemasa 1999
[a-Cyclodextrin](1).[1-Ethanol] 0.83 7.0 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Propanol ] 1.43 7.0 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Propanol ] 1.97 0.70 11.3 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Propanol ] 1.83 0.85 1.3 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Propylamine] 1.66 1.51 1.3 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Butylamine ] 1.71 2.04 1.3 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Pentylamine ] 2.01 0.60 1.3 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Hexylamine ] 2.60 0.70 1.3 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Heptylamine ] 3.07 1.43 1.3 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[1-Octylamine] 2.68 1.56 1.3 25.0 Calorimetry Giuseppina Castronuovo 2000
[a-Cyclodextrin](1).[p-N,Ndimethylaminobenzoic acid] 0.70 7.0 Fluorescence spectroscopy Minjoong Yoon 2001
[a-Cyclodextrin](1).[(1-[2-(4-chlorophenyl)methoxy]-2-(2,4-dichlorophenyl)ethyl)-1H-imidazole] 3.42 2.41 7.0 25.0 UV-vis spectroscopy P. Mura 2001
[a-Cyclodextrin](1).[(1-[2-(4-chlorophenyl)methoxy]-2-(2,4-dichlorophenyl)ethyl)-1H-imidazole] 3.12 7.0 37.0 UV-vis spectroscopy P. Mura 2001
[a-Cyclodextrin](1).[(1-[2-(4-chlorophenyl)methoxy]-2-(2,4-dichlorophenyl)ethyl)-1H-imidazole] 2.79 7.0 45.0 UV-vis spectroscopy P. Mura 2001
[a-Cyclodextrin](1).[(1-[2-(4-chlorophenyl)methoxy]-2-(2,4-dichlorophenyl)ethyl)-1H-imidazole] 2.63 1.58 25.0 UV-vis spectroscopy P. Mura 2001
[a-Cyclodextrin](1).[(1-[2-(4-chlorophenyl)methoxy]-2-(2,4-dichlorophenyl)ethyl)-1H-imidazole] 2.37 37.0 UV-vis spectroscopy P. Mura 2001
[a-Cyclodextrin](1).[(1-[2-(4-chlorophenyl)methoxy]-2-(2,4-dichlorophenyl)ethyl)-1H-imidazole] 2.27 45.0 UV-vis spectroscopy P. Mura 2001
[a-Cyclodextrin](1).[benzenesulfonate] 0.99 7.0 25.0 NMR spectroscopy Noriaki Funasaki 2001
[a-Cyclodextrin](1).[pancreatic a-amylase] 2.19 6.9 30.0 UV-vis spectroscopy Roger Koukiekolo 2001
[a-Cyclodextrin](1).[1-butanol-d10] 1.90 0.18 7.0 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[a-Cyclodextrin](1).[hexanoic acid-d11 ] 2.48 0.60 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[a-Cyclodextrin](1).[hexylamine ] 2.59 0.60 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[a-Cyclodextrin](1).[octanoic acid-d15 ] 3.39 2.11 6.9 25.0 Titration Calorimetry Yoshihisa Inoue 2002
[a-Cyclodextrin](1).[hexyltrimethylammonium bromide] -4.36 7.0 25.0 NMR spectroscopy Noriaki Funasaki 2003
[a-Cyclodextrin](1).[octyltrimethylammonium bromide] -2.44 7.0 25.0 NMR spectroscopy Noriaki Funasaki 2003
[a-Cyclodextrin](1).[octyltrimethylammonium bromide] 3.42 2.04 7.0 25.0 Calorimetry De-Zhi Sun 2005
[a-Cyclodextrin](1).[2-(2-cyclohexyl-2-hydroxy-2-phenylacetoxy)-N,N-diethyl-N-methylethanaminium bromide] 1.85 0.60 7.0 36.0 NMR spectroscopy Noriaki Funasaki 2003
[a-Cyclodextrin](1).[suberic acid] 3.52 3.00 9.0 80.0 electrospray ionization mass spectrometry Valérie Gabelica 2003
[a-Cyclodextrin](1).[azelaic acid] 3.41 2.78 9.0 80.0 electrospray ionization mass spectrometry Valérie Gabelica 2003
[a-Cyclodextrin](1).[sebacic acid] 3.30 2.60 9.0 80.0 electrospray ionization mass spectrometry Valérie Gabelica 2003
[a-Cyclodextrin](1).[1,2-pentanediol] 1.72 0.70 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[1,2-pentanediol] 1.89 0.70 7.0 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[1,2-hexanediol] 1.80 0.85 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[1,2-hexanediol] 2.27 1.63 7.0 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[1,2-octanediol ] 2.36 1.36 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[1,6-hexanediol] 1.85 1.00 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[1,6-hexanediol] 1.97 0.85 7.0 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[1,7-heptanediol ] 2.51 1.43 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[1,7-heptanediol ] 2.44 0.70 7.0 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[1,8-octanediol] 2.20 0.78 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[1,8-octanediol] 3.07 2.24 7.0 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[1,9-nonanediol ] 2.58 1.64 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[1,9-nonanediol ] 2.93 1.71 7.0 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[1,10-decanediol] 2.73 1.23 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[1,10-decanediol] 2.90 1.90 7.0 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[1,2-propanediol] 0.48 0.30 7.0 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[1,2-butanediol] 1.11 -0.40 7.0 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[1,3-propanediol] 0.63 -0.40 7.0 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[1,4-butanediol] 0.90 7.0 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[1,5-pentanediol] 1.49 7.0 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[1-cyclohexylethanol] 1.93 0.85 7.0 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[1-cyclohexylethanol] 1.51 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[4-cyclohexylbutan-1-ol] 2.99 2.20 7.0 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[4-cyclohexylbutan-1-ol] 2.30 1.11 25.0 Calorimetry Giuseppina Castronuovo 2002
[a-Cyclodextrin](1).[Pb(II) nitrate] 2.95 1.13 Cyclic voltammetry Maria Teresa Ramirez-Silva 2005
[a-Cyclodextrin](1).[dodecyltrimethylammonium bromide] 3.50 2.20 7.0 25.0 Calorimetry De-Zhi Sun 2005
[a-Cyclodextrin](2).[dodecyltrimethylammonium bromide] 6.69 5.40 7.0 25.0 Calorimetry De-Zhi Sun 2005
[a-Cyclodextrin](1).[tetradecyltrimethylammonium bromide] -2.64 7.0 25.0 Calorimetry De-Zhi Sun 2005
[a-Cyclodextrin](1).[tetradecyltrimethylammonium bromide] 4.63 3.16 25.0 Potentiometric titration Toshihiro Tominaga 1994
[a-Cyclodextrin](1).[tetradecyltrimethylammonium bromide] 4.79 isothermal titration calorimetry E. Wyn-Jones 1995
[a-Cyclodextrin](2).[tetradecyltrimethylammonium bromide] 6.81 5.51 7.0 25.0 Calorimetry De-Zhi Sun 2005
[a-Cyclodextrin](2).[tetradecyltrimethylammonium bromide] 3.50 2.96 25.0 Potentiometric titration Toshihiro Tominaga 1994
[a-Cyclodextrin](2).[tetradecyltrimethylammonium bromide] 3.85 isothermal titration calorimetry E. Wyn-Jones 1995
[a-Cyclodextrin](1).[ascorbic acid] 0.28 -0.70 7.0 25.0 Calorimetry I. V. Terekhova 2005
[a-Cyclodextrin](1).[eugenol] 4.69 7.0 20.0 UV-vis spectroscopy Le Xin Song 2005
[a-Cyclodextrin](1).[sodium dodecyl sulfate] 2.15 0.90 7.0 25.0 Fluorescence spectroscopy Daniel E. Otzen 2006
[a-Cyclodextrin](1).[sodium dodecyl sulfate] 4.52 7.0 25.0 Isothermal titration calorimetry Nobuhiko Yui 2000
[a-Cyclodextrin](1).[sodium lauroyl sarcosine] 2.36 1.08 7.0 25.0 Fluorescence spectroscopy Daniel E. Otzen 2006
[a-Cyclodextrin](1).[4-[4-(dimethylamino)phenylazo]benzoic acid] -2.24 -3.82 1.0 16.0 UV-vis spectroscopy Khalid M. Tawarah 1993
[a-Cyclodextrin](1).[4-[4-(dimethylamino)phenylazo]benzoic acid] -2.39 -3.96 1.0 25.0 UV-vis spectroscopy Khalid M. Tawarah 1993
[a-Cyclodextrin](1).[4-[4-(dimethylamino)phenylazo]benzoic acid] -2.51 -3.85 1.0 33.0 UV-vis spectroscopy Khalid M. Tawarah 1993
[a-Cyclodextrin](1).[4-[4-(dimethylamino)phenylazo]benzoic acid] -2.62 -4.15 1.0 40.5 UV-vis spectroscopy Khalid M. Tawarah 1993
[a-Cyclodextrin](1).[4-[4-(dimethylamino)phenylazo]benzoic acid] -1.91 -4.52 9.5 16.0 UV-vis spectroscopy Khalid M. Tawarah 1993
[a-Cyclodextrin](1).[4-[4-(dimethylamino)phenylazo]benzoic acid] -2.04 -3.66 9.5 25.0 UV-vis spectroscopy Khalid M. Tawarah 1993
[a-Cyclodextrin](1).[4-[4-(dimethylamino)phenylazo]benzoic acid] -2.12 -4.52 9.5 33.0 UV-vis spectroscopy Khalid M. Tawarah 1993
[a-Cyclodextrin](1).[4-[4-(dimethylamino)phenylazo]benzoic acid] -2.21 -4.00 9.5 40.5 UV-vis spectroscopy Khalid M. Tawarah 1993
[a-Cyclodextrin](1).[NADH] 0.45 6.0 25.0 HPLC-method Manabu Seno 1990
[a-Cyclodextrin](1).[NADP] 0.64 6.0 25.0 HPLC-method Manabu Seno 1990
[a-Cyclodextrin](1).[4-[4-(dimethylamino)phenylaza]benzenesulfonic acid sodium salt] 4.07 2.48 6.8 25.0 Conductivity measurements Khalid M. Tawarah 1993
[a-Cyclodextrin](1).[2-[4-(dimethylamino)phenylaza]benzoic acid sodium salt] 2.51 1.20 6.8 25.0 Conductivity measurements Khalid M. Tawarah 1993
[a-Cyclodextrin](1).[p-methyl red] 4.22 2.78 6.8 25.0 Conductivity measurements Khalid M. Tawarah 1993
[a-Cyclodextrin](2).[Diazepam] 0.30 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[a-Cyclodextrin](2).[Medazepam] 0.30 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[a-Cyclodextrin](1).[Nitrazepam ] 1.41 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[a-Cyclodextrin](1).[Nimetazepam ] 1.38 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[a-Cyclodextrin](1).[Flunitrazepam ] 1.32 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[a-Cyclodextrin](1).[Clonazepam ] 1.34 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[a-Cyclodextrin](1).[Flurazepam ] 1.00 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[a-Cyclodextrin](1).[Lorazepam ] 1.43 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[a-Cyclodextrin](1).[oxazepam ] 1.64 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[a-Cyclodextrin](1).[Clobazam ] 1.00 7.0 25.0 UV-vis spectroscopy M. Otagiri 1983
[a-Cyclodextrin](1).[( 5Z, 13E)-(9R, 11 R, 15R)-9-chloro-11,15-dihydroxy-16,16-dimethyl-5,13-prostadienoic acid] 3.22 7.0 15.0 UV-vis spectroscopy Kaneto Uekama 1990
[a-Cyclodextrin](1).[( 5Z, 13E)-(9R, 11 R, 15R)-9-chloro-11,15-dihydroxy-16,16-dimethyl-5,13-prostadienoic acid] 3.05 7.0 25.0 UV-vis spectroscopy Kaneto Uekama 1990
[a-Cyclodextrin](1).[( 5Z, 13E)-(9R, 11 R, 15R)-9-chloro-11,15-dihydroxy-16,16-dimethyl-5,13-prostadienoic acid] 2.92 7.0 35.0 UV-vis spectroscopy Kaneto Uekama 1990
[a-Cyclodextrin](1).[hydrocortisone butyrate ] 2.51 4.0 20.0 Solubility method (UV-vis spectroscopy) In Koo Chun 1993
[a-Cyclodextrin](1).[hydrocortisone butyrate ] 2.45 4.0 30.0 Solubility method (UV-vis spectroscopy) In Koo Chun 1993
[a-Cyclodextrin](1).[hydrocortisone butyrate ] 2.40 4.0 37.0 Solubility method (UV-vis spectroscopy) In Koo Chun 1993
[a-Cyclodextrin](1).[L-Phe ] 1.11 -0.40 7.4 23.0 UV-vis spectroscopy Jiri Horsky 1994
[a-Cyclodextrin](1).[Gly-L-Phe ] 1.30 -0.22 7.4 23.0 UV-vis spectroscopy Jiri Horsky 1994
[a-Cyclodextrin](1).[Gly-D-Phe ] 1.36 -0.15 7.4 23.0 UV-vis spectroscopy Jiri Horsky 1994
[a-Cyclodextrin](1).[L-PheGly ] 1.15 -0.15 7.4 23.0 UV-vis spectroscopy Jiri Horsky 1994
[a-Cyclodextrin](1).[GlyGly-L-Phe ] 1.67 -0.10 7.4 23.0 UV-vis spectroscopy Jiri Horsky 1994
[a-Cyclodextrin](1).[Gly-L-Tyr ] 1.11 -0.70 7.4 23.0 UV-vis spectroscopy Jiri Horsky 1994
[a-Cyclodextrin](1).[L-TrpGly ] 1.32 0.04 7.4 23.0 UV-vis spectroscopy Jiri Horsky 1994
[a-Cyclodextrin](1).[Aspartame] 1.62 -0.15 7.4 23.0 UV-vis spectroscopy Jiri Horsky 1994
[a-Cyclodextrin](1).[Adenine ] 0.51 -0.30 7.0 25.0 UV-vis spectroscopy Bradley D. Anderson 1990
[a-Cyclodextrin](1).[monobutylurea] 2.10 7.0 25.0 Calorimetry Massimo Muscetta 1986
[a-Cyclodextrin](1).[monopropylurea] 1.11 7.0 25.0 Calorimetry Massimo Muscetta 1986
[a-Cyclodextrin](1).[monoethylurea] 0.45 7.0 25.0 Calorimetry Massimo Muscetta 1986
[a-Cyclodextrin](1).[Diphenidol HCl] 1.64 -0.10 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[a-Cyclodextrin](1).[Diphenhydramine HCI] 1.65 -0.22 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[a-Cyclodextrin](1).[Orphenadrine HCI ] 1.55 -0.22 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[a-Cyclodextrin](1).[Bromodiphenhydramine HCl ] 3.13 1.95 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[a-Cyclodextrin](1).[Diphenylpyraline HCI ] 1.50 -0.10 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[a-Cyclodextrin](1).[Cyclizine HCl] 1.68 0.56 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[a-Cyclodextrin](1).[Chlorcyclizine HCI] 3.05 1.82 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[a-Cyclodextrin](1).[Chlorcyclizine 2HCl] 3.05 0.98 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[a-Cyclodextrin](1).[Meclizine 2HCl] 2.94 1.14 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[a-Cyclodextrin](1).[Hydroxyzine HCI] 3.06 1.78 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[a-Cyclodextrin](1).[Hydroxyzine 2HCl ] 3.06 1.57 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[a-Cyclodextrin](1).[Proadifen HCl] 2.27 0.90 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[a-Cyclodextrin](1).[Adiphenine HCl ] 1.06 -0.10 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[a-Cyclodextrin](1).[Terfenadine HCl] 1.72 -0.30 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[a-Cyclodextrin](1).[amitriptylin] 1.79 6.0 25.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[a-Cyclodextrin](1).[notriptylin] 1.94 0.95 6.0 25.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[a-Cyclodextrin](1).[doxepin] 1.70 0.30 6.0 25.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[a-Cyclodextrin](1).[imipramin] 1.91 0.30 6.0 25.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[a-Cyclodextrin](1).[protriptylin] 2.03 0.95 6.0 25.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[a-Cyclodextrin](1).[maprotilin] 2.09 0.90 6.0 25.0 Measurements with ion selective electrode Panayotis E. Macheras 1992
[a-Cyclodextrin](1).[Cinnarizine 2HCl] 1.45 -0.10 7.0 25.0 Calorimetry Bradley D. Anderson 1993
[a-Cyclodextrin](1).[fenoprofen calcium dihydrate] 2.40 1.26 7.4 25.0 UV-vis spectroscopy David Diaz 1999
[a-Cyclodextrin](1).[fenoprofen calcium dihydrate] 2.68 1.69 7.4 25.0 Fluorescence spectroscopy David Diaz 1999
[a-Cyclodextrin](1).[L-tyrosine ] 1.43 0.48 7.0 20.0 Fluorescence spectroscopy Frank V. Bright 1996
[a-Cyclodextrin](1).[L-tyrosine ] 1.36 0.60 10.0 20.0 Fluorescence spectroscopy Frank V. Bright 1996
[a-Cyclodextrin](1).[YIGSR ] 1.30 0.60 7.0 20.0 Fluorescence spectroscopy Frank V. Bright 1996
[a-Cyclodextrin](1).[YIGSR ] 1.28 0.60 10.0 20.0 Fluorescence spectroscopy Frank V. Bright 1996
[a-Cyclodextrin](1).[YGGFL] 1.30 0.48 7.0 20.0 Fluorescence spectroscopy Frank V. Bright 1996
[a-Cyclodextrin](1).[YGGFL] 1.30 0.48 10.0 20.0 Fluorescence spectroscopy Frank V. Bright 1996
[a-Cyclodextrin](1).[N-methyil-p-(p-dimethylaminophenyl)-pyridinium iodide] 0.85 7.0 27.0 Fluorescence spectroscopy Michael I. Knyazhansky 1993
[a-Cyclodextrin](1).[tryptophan] 1.63 0.78 7.0 30.0 NMR spectroscopy Akira Harada 2006
[a-Cyclodextrin](1).[phenylalanine] 1.20 0.70 7.0 30.0 NMR spectroscopy Akira Harada 2006
[a-Cyclodextrin](1).[poly(N-methacryloyltryptophan)] 1.48 0.30 7.0 30.0 NMR spectroscopy Akira Harada 2006
[a-Cyclodextrin](1).[p-Nitrobenzoate] 1.82 0.04 9.2 25.0 UV-vis spectroscopy Agustín G. Asuero 2006
[a-Cyclodextrin](1).[p-Nitrophenol] 2.36 0.01 7.0 25.0 UV-vis spectroscopy Agustín G. Asuero 2006
[a-Cyclodextrin](1).[4-Acetylbenzoate] 1.70 0.02 9.18 25.0 UV-vis spectroscopy Agustín G. Asuero 2006
[a-Cyclodextrin](1).[R-1-T3] 1.31 George W. Gokel 2003
[a-Cyclodextrin](1).[S-1-T3] 1.20 George W. Gokel 2003
[a-Cyclodextrin](1).[R-3-T3] 1.34 George W. Gokel 2003
[a-Cyclodextrin](1).[S-3-T3] 1.51 George W. Gokel 2003
[a-Cyclodextrin](1).[R-5-T3] 1.92 George W. Gokel 2003
[a-Cyclodextrin](1).[S-5-T3] 1.87 George W. Gokel 2003
[a-Cyclodextrin](1).[R-6-T3] 1.09 George W. Gokel 2003
[a-Cyclodextrin](1).[S-6-T3] 1.03 George W. Gokel 2003
[a-Cyclodextrin](1).[R-1-T5] 1.41 George W. Gokel 2003
[a-Cyclodextrin](1).[S-1-T5] 1.53 George W. Gokel 2003
[a-Cyclodextrin](1).[R-2-T5] 0.90 George W. Gokel 2003
[a-Cyclodextrin](1).[S-2-T5] 0.92 George W. Gokel 2003
[a-Cyclodextrin](1).[R-3-T5] 1.75 George W. Gokel 2003
[a-Cyclodextrin](1).[S-3-T5] 1.76 George W. Gokel 2003
[a-Cyclodextrin](1).[R-4-T5] 1.38 George W. Gokel 2003
[a-Cyclodextrin](1).[S-4-T5] 1.40 George W. Gokel 2003
[a-Cyclodextrin](1).[R-5-T5] 2.60 George W. Gokel 2003
[a-Cyclodextrin](1).[S-5-T5] 2.30 George W. Gokel 2003
[a-Cyclodextrin](1).[R-6-T5] 2.05 George W. Gokel 2003
[a-Cyclodextrin](1).[S-6-T5] 1.96 George W. Gokel 2003
[a-Cyclodextrin](1).[1,4-diaminobutane] 1.18 0.14 7.0 25.0 NMR diffusion measurements Cohen, Yoram 2002
[a-Cyclodextrin](1).[1,6-diaminohexane] 1.81 0.07 7.0 25.0 NMR diffusion measurements Cohen, Yoram 2002
[a-Cyclodextrin](1).[1,8-diaminooctane] 2.83 0.21 7.0 25.0 NMR diffusion measurements Cohen, Yoram 2002
[a-Cyclodextrin](1).[1,8-diaminooctane] 1.75 0.18 25.0 NMR diffusion measurements Cohen, Yoram 2002
[a-Cyclodextrin](1).[1,10-diaminodecane] 4.13 0.30 7.0 25.0 NMR diffusion measurements Cohen, Yoram 2002
[a-Cyclodextrin](1).[1,10-diaminodecane] 3.31 0.05 25.0 NMR diffusion measurements Cohen, Yoram 2002
[a-Cyclodextrin](1).[1,12-diaminododecane] 3.85 0.27 7.0 25.0 NMR diffusion measurements Cohen, Yoram 2002
[a-Cyclodextrin](1).[1,12-diaminododecane] 3.86 0.06 25.0 NMR diffusion measurements Cohen, Yoram 2002
[a-Cyclodextrin](1).[R-C8] 1.20 0.48 7.0 25.0 NMR spectroscopy George W. Gokel 2003
[a-Cyclodextrin](1).[S-C8] 1.18 0.48 7.0 25.0 NMR spectroscopy George W. Gokel 2003
[a-Cyclodextrin](1).[R-C1] 1.34 0.30 7.0 25.0 NMR spectroscopy George W. Gokel 2003
[a-Cyclodextrin](1).[1,8-diaminooctane*HCl] 1.87 0.15 7.0 25.0 NMR diffusion measurements Cohen, Yoram 2002
[a-Cyclodextrin](1).[S-C1] 1.28 0.30 7.0 25.0 NMR spectroscopy George W. Gokel 2003
[a-Cyclodextrin](1).[1,10-diaminodecane*HCl] 3.34 0.19 7.0 25.0 NMR diffusion measurements Cohen, Yoram 2002
[a-Cyclodextrin](1).[pyridinephenolates] 2.20 1.38 7.0 25.0 UV-vis spectroscopy Marcos Caroli Rezende 2006
[a-Cyclodextrin](1).[acetic acid] 1.50 0.46 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[acetic acid] 1.16 0.28 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[a-Cyclodextrin](1).[propinoic acid] 1.54 0.60 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[butyric acid] 2.07 0.77 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[isobutyric acid] 1.16 -0.10 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[valeric acid] 2.50 1.32 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[isovaleric acid] 1.55 0.08 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[lactic acid] 1.37 0.72 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[succinic acid] 1.81 0.04 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[succinic acid] 2.24 1.21 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[a-Cyclodextrin](1).[cadaverine] 1.46 0.45 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[putrescine] 1.51 0.71 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[pyridine ] 1.10 0.20 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[3-methyl-pyridine] 1.27 0.11 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[diphenylamine] 1.38 0.38 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[hydrogen sulfide] 1.32 -0.12 22.0 HS-GCMS Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[methanethiol] 1.36 -0.52 22.0 HS-GCMS Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[dimethyl sulfide] 1.40 0.34 22.0 HS-GCMS Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[phenyl acetate] 0.84 0.08 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[m-cresol] 1.68 0.36 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[phenol ] 1.27 0.11 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[indole] 0.74 -0.10 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[skatole] 0.61 -0.22 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[dodecanol] 2.15 1.31 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[tatradecanol] 2.63 1.85 7.0 22.0 NMR titration Daniel W. Armstrong 2006
[a-Cyclodextrin](1).[p-nitrobenzene derivative 1] 3.00 1.40 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[a-Cyclodextrin](0.5).[p-nitrobenzene derivative 1] 1.18 0.08 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[a-Cyclodextrin](1).[p-nitrobenzene derivative 2] 3.07 1.60 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[a-Cyclodextrin](1).[p-nitrobenzene derivative 3] 3.16 1.54 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[a-Cyclodextrin](0.5).[p-nitrobenzene derivative 3] 1.52 0.15 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[a-Cyclodextrin](1).[p-nitrobenzene derivative 4] 3.06 1.78 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[a-Cyclodextrin](1).[p-nitrobenzene derivative 5] 2.50 1.70 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[a-Cyclodextrin](1).[p-nitrobenzene derivative 6] 2.70 1.85 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[a-Cyclodextrin](1).[p-nitrobenzene derivative 7] 3.08 1.48 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[a-Cyclodextrin](0.5).[p-nitrobenzene derivative 7] 1.89 0.28 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[a-Cyclodextrin](1).[p-nitrobenzene derivative 8] 3.33 2.08 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[a-Cyclodextrin](0.5).[p-nitrobenzene derivative 8] 2.37 1.18 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[a-Cyclodextrin](1).[p-nitrobenzene derivative 9] 3.13 1.40 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[a-Cyclodextrin](1).[p-nitrobenzene derivative 11] 3.56 1.95 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[a-Cyclodextrin](1).[p-nitrobenzene derivative 12] 3.00 1.60 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[a-Cyclodextrin](1).[p-nitrobenzene derivative 12] 3.00 1.78 2.5 25.0 UV-vis spectroscopy Renato Noto 2003
[a-Cyclodextrin](0.5).[p-nitrobenzene derivative 12] 1.41 0.08 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[a-Cyclodextrin](0.5).[p-nitrobenzene derivative 12] 1.93 0.70 2.5 25.0 UV-vis spectroscopy Renato Noto 2003
[a-Cyclodextrin](1).[p-nitrobenzene derivative 13] 3.07 1.18 6.0 25.0 UV-vis spectroscopy Renato Noto 2003
[a-Cyclodextrin](1).[p-nitrobenzene derivative 13] 3.02 1.40 2.5 25.0 UV-vis spectroscopy Renato Noto 2003
[a-Cyclodextrin](1).[4-chlorophenol] 2.15 7.0 22.0 Circular dichroism spectroscopy Sandra Monti 2005
[a-Cyclodextrin](1).[4-chlorophenol] 2.44 1.41 2.0 20.0 UV-vis spectroscopy Miguel A. Garcia-Garibay 2001
[a-Cyclodextrin](1).[4-chlorophenol] 2.52 1.18 7.0 20.0 NMR spectroscopy Miguel A. Garcia-Garibay 2001
[a-Cyclodextrin](1).[4-chlorophenol] 2.51 23.0 NIR spectroscopy Chieu D. Tran 1995
[a-Cyclodextrin](1).[styrene] 2.46 Kasi Pitchumani 2005
[a-Cyclodextrin](1).[methyl cinnamate] 2.33 Kasi Pitchumani 2005
[a-Cyclodextrin](1).[phenylacetylene] 2.27 Kasi Pitchumani 2005
[a-Cyclodextrin](1).[allylbenzene] 2.35 Kasi Pitchumani 2005
[a-Cyclodextrin](1).[cyclosporin A] 2.46 7.0 25.0 HPLC method Laura Matilainen 2006
[a-Cyclodextrin](1).[cyclosporin A] 1.68 25.0 HPLC-method Yingqing Ran 2001
[a-Cyclodextrin](0.5).[cyclosporin A] 1.63 7.0 25.0 HPLC method Laura Matilainen 2006
[a-Cyclodextrin](1).[E-4-tertbutylphenyl-4' -oxyazobenzene] 5.45 4.45 10.0 25.0 UV-vis spectroscopy Stephen F. Lincoln 2005
[a-Cyclodextrin](2).[E-4-tertbutylphenyl-4' -oxyazobenzene] 3.84 1.78 10.0 25.0 UV-vis spectroscopy Stephen F. Lincoln 2005
[a-Cyclodextrin](1).[p-dimethylaminobenzonitrile] 3.04 0.10 7.0 20.0 Fluorescence spectroscopy Sandra Monti 2003
[a-Cyclodextrin](1).[p-dimethylaminobenzonitrile] 4.46 0.18 7.0 20.0 UV-vis spectroscopy Sandra Monti 2003
[a-Cyclodextrin](1).[p-dimethylaminobenzonitrile] 4.02 0.74 7.0 20.0 Circular dichroism spectroscopy Sandra Monti 2003
[a-Cyclodextrin](2).[p-dimethylaminobenzonitrile] 4.67 0.13 7.0 20.0 Fluorescence spectroscopy Sandra Monti 2003
[a-Cyclodextrin](2).[p-dimethylaminobenzonitrile] 6.80 0.30 7.0 20.0 Triplet–triplet absorption spectroscopy Sandra Monti 2003
[a-Cyclodextrin](2).[p-dimethylaminobenzonitrile] 7.21 0.19 7.0 20.0 UV-vis spectroscopy Sandra Monti 2003
[a-Cyclodextrin](2).[p-dimethylaminobenzonitrile] 6.66 0.77 7.0 20.0 Circular dichroism spectroscopy Sandra Monti 2003
[a-Cyclodextrin](1).[nitrazine yellow] 1.88 0.02 9.2 UV-vis spectroscopy Agustín G. Asuero 2006
[a-Cyclodextrin](1).[methyl orange] 2.83 0.00 1.0 25.0 UV-vis spectroscopy Agustín G. Asuero 2006
[a-Cyclodextrin](1).[methyl orange] 3.01 1.08 0.7 25.0 UV and NMR spectroscopy Yoshihisa Matsui 1994
[a-Cyclodextrin](1).[methyl orange] -0.11 -0.75 spectrophotometry C.van Hooidonk 1970
[a-Cyclodextrin](1).[p-nitrobenzoate] 1.89 0.03 9.2 UV-vis spectroscopy Agustín G. Asuero 2006
[a-Cyclodextrin](1).[4-acetylbenzoate] 1.70 0.02 9.18 25.0 UV-vis spectroscopy Agustín G. Asuero 2006
[a-Cyclodextrin](1).[b-lapachone] 1.30 -0.15 7.4 25.0 UV-vis spectroscopy Jinming Gao 2003
[a-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] 1.63 1.30 8.7 30.0 UV-vis spectroscopy Mahmoud M. Al Omari 2006
[a-Cyclodextrin](2).[cyclosporin A] 1.26 25.0 HPLC-method Yingqing Ran 2001
[a-Cyclodextrin](1).[fenoprofen] 2.06 0.90 2.0 20.0 Fluorescence spectroscopy Jana Sadecka 2005
[a-Cyclodextrin](1).[fenoprofen] 1.90 1.00 7.0 20.0 Fluorescence spectroscopy Jana Sadecka 2005
[a-Cyclodextrin](1).[dibenzofuran-2-carboxylic acid] 3.04 1.90 2.0 25.0 Fluorescence spectroscopy Gustavo González-Gaitano 2004
[a-Cyclodextrin](1).[(+)-menthone] 0.58 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](2).[(+)-menthone] 0.95 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](1).[(-)-menthone] 0.64 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](2).[(-)-menthone] 0.79 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](1).[(+)-isomnethone] 0.81 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](2).[(+)-isomnethone] 0.95 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](1).[(-)-isomnethone] 0.87 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](2).[(-)-isomnethone] 1.04 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](1).[(+)-fenchone] 1.53 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](2).[(+)-fenchone] 1.00 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](2).[(-)-fenchone] 1.04 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](1).[(±)-pulegone] 0.53 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](1).[(+)-a-pinene] 1.92 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](2).[(+)-a-pinene] 1.32 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](1).[(-)-a-pinene] 2.21 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](2).[(-)-a-pinene] 1.41 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](1).[(+)-b-pinene] 2.04 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](2).[(+)-b-pinene] 0.95 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](1).[(-)-b-pinene] 2.32 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](2).[(-)-b-pinene] 1.00 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](1).[(+)-limonene] 1.30 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](2).[(+)-limonene] 1.20 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](1).[(-)-limonene] 1.26 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](2).[(-)-limonene] 1.18 60.0 Gas chromatography Monika Asztemborska 2005
[a-Cyclodextrin](1).[N,N'-Diheptyl-4,4'-bipyridinium] 3.52 2.45 8.0 25.0 UV-vis spectroscopy Iwao Suzuki 2006
[a-Cyclodextrin](2).[N,N'-Diheptyl-4,4'-bipyridinium] 2.99 1.92 8.0 25.0 UV-vis spectroscopy Iwao Suzuki 2006
[a-Cyclodextrin](1).[heptanol] 3.26 2.45 8.0 25.0 UV-vis spectroscopy Iwao Suzuki 2006
[a-Cyclodextrin](1).[4,4'-azodibenzoic acid] 4.00 7.0 UV-vis spectroscopy Akira Harada 2005
[a-Cyclodextrin](1).[N,N'-Dibutyl-1,4,5,8-naphthalenediimide] 3.12 7.0 23.0 UV-vis spectroscopy Mario J. Politi 1999
[a-Cyclodextrin](2).[N,N'-Dibutyl-1,4,5,8-naphthalenediimide] 2.52 7.0 23.0 UV-vis spectroscopy Mario J. Politi 1999
[a-Cyclodextrin](1).[N-Butyl-1,8-naphthalimide] 2.67 7.0 23.0 UV-vis spectroscopy Mario J. Politi 1999
[a-Cyclodextrin](1).[N-Butyl-1,8-naphthalimide] 2.72 3.0 23.0 UV-vis spectroscopy Mario J. Politi 1999
[a-Cyclodextrin](1).[2,3-diazabicyclo[2.2.2]oct-2-ene] 1.70 1.00 7.0 25.0 NMR spectroscopy Werner M. Nau 1999
[a-Cyclodextrin](1).[2,4-dichlorophenoxyacetic acid] 1.98 7.0 25.0 UV-vis spectroscopy J. I. Perez-Martinez 2000
[a-Cyclodextrin](2).[2,4-dichlorophenoxyacetic acid] 0.81 7.0 25.0 UV-vis spectroscopy J. I. Perez-Martinez 2000
[a-Cyclodextrin](1).[3-chlorophenol] 2.30 1.20 2.0 20.0 UV-vis spectroscopy Miguel A. Garcia-Garibay 2001
[a-Cyclodextrin](1).[3-chlorophenol] 2.51 1.15 2.0 20.0 NMR spectroscopy Miguel A. Garcia-Garibay 2001
[a-Cyclodextrin](1).[2-chlorophenol] 1.54 0.60 2.0 20.0 UV-vis spectroscopy Miguel A. Garcia-Garibay 2001
[a-Cyclodextrin](1).[3,4-dichlorophenol] 2.08 1.18 2.0 20.0 UV-vis spectroscopy Miguel A. Garcia-Garibay 2001
[a-Cyclodextrin](1).[2,4-dichlorophenol] 2.32 1.43 2.0 20.0 UV-vis spectroscopy Miguel A. Garcia-Garibay 2001
[a-Cyclodextrin](1).[2,4-dichlorophenol] 2.61 1.23 7.0 20.0 NMR spectroscopy Miguel A. Garcia-Garibay 2001
[a-Cyclodextrin](1).[2,6-dichlorophenol] 2.00 1.11 2.0 20.0 UV-vis spectroscopy Miguel A. Garcia-Garibay 2001
[a-Cyclodextrin](1).[nimodipine] 1.79 1.15 7.0 25.0 UV-vis spectroscopy Frantisek Kopecky 2001
[a-Cyclodextrin](1).[α-asarone] 2.88 7.2 25.0 Fluorescence spectroscopy Yu Liu 2003
[a-Cyclodextrin](1).[ferulic acid] 3.05 7.2 25.0 Fluorescence spectroscopy Yu Liu 2003
[a-Cyclodextrin](1).[magnolol] 3.62 7.2 25.0 Fluorescence spectroscopy Yu Liu 2003
[a-Cyclodextrin](1).[honokiol] 3.96 7.2 25.0 Fluorescence spectroscopy Yu Liu 2003
[a-Cyclodextrin](1).[L-phenylalanine] 1.16 -0.40 7.8 17.0 NMR spectroscopy Reinhard Wimmer 2002
[a-Cyclodextrin](1).[L-phenylalanine] 1.18 7.0 Calorimetry Reinhard Wimmer 2002
[a-Cyclodextrin](1).[L-phenylalanine] 0.90 0.48 13.6 Calorimetry Reinhard Wimmer 2002
[a-Cyclodextrin](1).[L-phenylalanine] 1.40 11.3 Calorimetry Reinhard Wimmer 2002
[a-Cyclodextrin](1).[L-phenylalanine] 1.20 0.04 11.0 Spectral inhibition titration Reinhard Wimmer 2002
[a-Cyclodextrin](1).[L-phenylalanine] 1.19 -0.70 11.0 Calorimetry Reinhard Wimmer 2002
[a-Cyclodextrin](1).[L-phenylalanine] 1.63 7.2 Calorimetry Reinhard Wimmer 2002
[a-Cyclodextrin](1).[L-phenylalanine] 0.90 0.70 5.0 Calorimetry Reinhard Wimmer 2002
[a-Cyclodextrin](1).[L-phenylalanine] 1.00 7.0 Diffusion followed by Gouey-interferometry Reinhard Wimmer 2002
[a-Cyclodextrin](1).[L-phenylalanine] 0.90 0.70 5.01 25.0 Titration calorimetry Robert N. Goldberg 1994
[a-Cyclodextrin](1).[L-phenylalanine] 4.18 7.0 25.0 microcalorimetry Giuseppina Castronuovo 1995
[a-Cyclodextrin](1).[L-phenylalanine] 4.40 11.3 25.0 microcalorimetry Giuseppina Castronuovo 1995
[a-Cyclodextrin](1).[L-phenylalanine] 3.90 13.6 25.0 microcalorimetry Giuseppina Castronuovo 1995
[a-Cyclodextrin](1).[L-phenylalanine] 1.21 0.30 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[a-Cyclodextrin](1).[acridine red] 1.70 6.0 25.0 Fluorescence spectroscopy Yu Liu 2002
[a-Cyclodextrin](1).[sodium 6-p-toluidino-2-naphthalenesulfonic acid] 1.73 6.0 25.0 Fluorescence spectroscopy Yu Liu 2002
[a-Cyclodextrin](1).[p-Methyl red-modified b-CD] 2.30 1.0 25.0 Induced circular dichroism Tetsuo Kuwabara 2002
[a-Cyclodextrin](1).[p-Methyl red-modified b-CD] 2.48 6.59 25.0 Induced circular dichroism Tetsuo Kuwabara 2002
[a-Cyclodextrin](1).[p-Nitorophenol-modified b-CD] 1.82 4.6 25.0 Induced circular dichroism Tetsuo Kuwabara 2002
[a-Cyclodextrin](1).[p-Nitorophenol-modified b-CD] 1.20 6.5 25.0 Induced circular dichroism Tetsuo Kuwabara 2002
[a-Cyclodextrin](1).[1,10-bis(trimethylammonium)decane] 3.19 2.60 7.0 25.0 NMR spectroscopy G. Wenz 1997
[a-Cyclodextrin](1).[1,10-bis(trimethylammonium)decane] 2.85 1.63 7.2 35.0 Microcalorimetric titrations G. Wenz 1997
[a-Cyclodextrin](1).[1,10-bis(trimethylammonium)decane] 2.65 7.2 50.0 Microcalorimetric titrations G. Wenz 1997
[a-Cyclodextrin](1).[atrazine] 3.69 7.0 Polarography L. Pospisil 1998
[a-Cyclodextrin](1).[Naphtalene-1-sulfonate] 1.56 0.51 3.0 25.0 Capillary electrophoresis Wang-Hsien Ding 2004
[a-Cyclodextrin](1).[Naphtalene-2-sulfonate] 1.57 0.45 3.0 25.0 Capillary electrophoresis Wang-Hsien Ding 2004
[a-Cyclodextrin](1).[Naphtalene-1,5-disulfonate] 1.61 0.85 3.0 25.0 Capillary electrophoresis Wang-Hsien Ding 2004
[a-Cyclodextrin](1).[Naphtalene-1,6-disulfonate] 1.62 0.99 3.0 25.0 Capillary electrophoresis Wang-Hsien Ding 2004
[a-Cyclodextrin](1).[N-carboxybenzoyl-L-glutamic acid] 1.18 0.30 6.9 25.0 Isothermal titration calorimetry Yoshihisa Inoue 2004
[a-Cyclodextrin](1).[Naphtalene-2,6-disulfonate] 1.57 0.91 3.0 25.0 Capillary electrophoresis Wang-Hsien Ding 2004
[a-Cyclodextrin](1).[N-carboxybenzoyl-D-glutamic acid] 1.15 0.30 6.9 25.0 Isothermal titration calorimetry Yoshihisa Inoue 2004
[a-Cyclodextrin](1).[N-acetyl-D-tyrosine] 0.95 0.30 6.9 25.0 Isothermal titration calorimetry Yoshihisa Inoue 2004
[a-Cyclodextrin](1).[N-acetyl-L-tyrosine] 0.85 0.30 6.9 25.0 Isothermal titration calorimetry Yoshihisa Inoue 2004
[a-Cyclodextrin](1).[N-carboxybenzoyl-D-glutamyl-L-tyrosine] 1.23 0.30 6.9 25.0 Isothermal titration calorimetry Yoshihisa Inoue 2004
[a-Cyclodextrin](1).[N-carboxybenzoyl-L-glutamyl-L-tyrosine] 1.24 0.18 6.9 25.0 Isothermal titration calorimetry Yoshihisa Inoue 2004
[a-Cyclodextrin](1).[3-aminonaphtalene-2,7-disulfonate] 1.58 0.94 3.0 25.0 Capillary electrophoresis Wang-Hsien Ding 2004
[a-Cyclodextrin](1).[5,10,15-tris(3,5-dicarboxylatophenyl)-20-phenylporphyrin] 1.52 0.60 7.0 25.0 Isothermal titration calorimetry Koji Kano 2005
[a-Cyclodextrin](1).[2-aminonaphtalene-1,5-disulfonate] 1.47 0.91 3.0 25.0 Capillary electrophoresis Wang-Hsien Ding 2004
[a-Cyclodextrin](1).[triclosan] 2.59 7.0 25.0 UV-vis spectroscopy P. Mura 2005
[a-Cyclodextrin](1).[phenol] 1.94 23.0 NIR spectroscopy Chieu D. Tran 1995
[a-Cyclodextrin](1).[phenol] 1.61 0.28 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[phenol] 1.57 0.60 Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[phenolate] 1.63 23.0 NIR spectroscopy Chieu D. Tran 1995
[a-Cyclodextrin](1).[4-chlorophenolate] 2.18 23.0 NIR spectroscopy Chieu D. Tran 1995
[a-Cyclodextrin](1).[phenolphthalein] 2.03 10.4 VIS spectroscopy Tsuneo Okubo 1989
[a-Cyclodextrin](1).[trans-[[[4'-[(4-ethylphenyl)azo]phenyl]oxy]ethyl]trimethylammonuim bromide] 1.57 25.0 Induced circular dichroism Keishiro Shiahama 1996
[a-Cyclodextrin](1).[trans-[[[4'-[(4-ethylphenyl)azo]phenyl]oxy]ethyl]trimethylammonuim bromide] 1.51 25.0 Electromotive force potentiometric titration Keishiro Shiahama 1996
[a-Cyclodextrin](1).[trans-[[[4'-[(4-butylphenyl)azo]phenyl]oxy]ethyl]trimethylammonuim bromide] 1.70 25.0 Induced circular dichroism Keishiro Shiahama 1996
[a-Cyclodextrin](1).[trans-[[[4'-[(4-butylphenyl)azo]phenyl]oxy]ethyl]trimethylammonuim bromide] 1.57 25.0 Electromotive force potentiometric titration Keishiro Shiahama 1996
[a-Cyclodextrin](1).[(S)-(+)-2-heptanol] 2.88 2.10 6.9 25.0 Titration calorimetry Robert N. Goldberg 1994
[a-Cyclodextrin](1).[(R)-(-)-2-heptanol] 2.88 2.28 6.9 25.0 Titration calorimetry Robert N. Goldberg 1994
[a-Cyclodextrin](1).[3-nitrophenolate] 2.30 0.70 11.1 27.8 Capillary electrophoresis David M. Goodall 1995
[a-Cyclodextrin](1).[4-nitrophenolate] 3.20 1.30 11.1 27.8 Capillary electrophoresis David M. Goodall 1995
[a-Cyclodextrin](1).[2-butanol] 1.32 0.30 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[2-pentanol] 2.03 0.90 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[3-pentanol] 1.65 0.30 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[3-methyl-1-butanol] 1.76 0.60 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[2-hexanol] 2.61 0.95 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[3-hexanol] 2.20 1.04 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[2-methyl-2-pentanol] 2.39 0.70 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[3-methyl-2-pentanol] 2.18 0.70 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[3,3-dimethyl-1-butanol] 1.89 0.70 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[4-methyl-1-pentanol] 2.18 0.60 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[4-methyl-2-pentanol] 1.76 0.48 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[2-heptanol] 2.85 0.95 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[3-heptanol] 2.71 0.90 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[4-heptanol] 2.58 0.85 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[2-octanol] 3.30 1.36 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[3-octanol] 2.97 1.04 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[4-octanol] 2.73 0.70 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[1-nonanol] 3.83 2.11 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[2-nonanol] 3.55 1.64 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[3-nonanol] 3.33 1.38 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[4-nonanol] 3.00 1.08 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[5-nonanol] 2.84 1.20 25.0 Surface tension Yoshihiro Saito 2000
[a-Cyclodextrin](1).[methyl tert-butyl ether] 2.10 25.0 GC Ji-Won Yang 2003
[a-Cyclodextrin](1).[n-hexane] 1.65 0.70 25.0 GC (SHSGC) É. Fenyvesi 2005
[a-Cyclodextrin](4).[praziquantel] 1.75 30.0 UV spectroscopy Gordon Becket 1999
[a-Cyclodextrin](1).[n-heptane] 2.44 1.57 25.0 GC (SHSGC) É. Fenyvesi 2005
[a-Cyclodextrin](1).[n-octane] 2.73 1.72 25.0 GC (SHSGC) É. Fenyvesi 2005
[a-Cyclodextrin](1).[n-nonane] 3.07 1.76 25.0 GC (SHSGC) É. Fenyvesi 2005
[a-Cyclodextrin](1).[n-decane] 3.12 2.16 25.0 GC (SHSGC) É. Fenyvesi 2005
[a-Cyclodextrin](1).[n-undecane] 3.30 2.22 25.0 GC (SHSGC) É. Fenyvesi 2005
[a-Cyclodextrin](1).[n-dodecane] 3.34 2.46 25.0 GC (SHSGC) É. Fenyvesi 2005
[a-Cyclodextrin](1).[cyclohexane] 2.21 1.36 25.0 GC (SHSGC) É. Fenyvesi 2005
[a-Cyclodextrin](1).[Me-cyclohexane] 2.15 0.85 25.0 GC (SHSGC) É. Fenyvesi 2005
[a-Cyclodextrin](1).[Et-cyclohexane] 3.30 2.37 25.0 GC (SHSGC) É. Fenyvesi 2005
[a-Cyclodextrin](1).[benzene] 1.30 0.85 25.0 GC (SHSGC) É. Fenyvesi 2005
[a-Cyclodextrin](1).[toluene] 1.46 0.90 25.0 GC (SHSGC) É. Fenyvesi 2005
[a-Cyclodextrin](1).[o-xylene] 0.99 0.43 25.0 GC (SHSGC) É. Fenyvesi 2005
[a-Cyclodextrin](1).[m-xylene] 1.56 0.60 25.0 GC (SHSGC) É. Fenyvesi 2005
[a-Cyclodextrin](1).[p-xylene] 2.12 1.26 25.0 GC (SHSGC) É. Fenyvesi 2005
[a-Cyclodextrin](1).[Et-benzene] 2.12 1.28 25.0 GC (SHSGC) É. Fenyvesi 2005
[a-Cyclodextrin](1).[1,3,5-trimethyl-benzene] 1.75 0.85 25.0 GC (SHSGC) É. Fenyvesi 2005
[a-Cyclodextrin](1).[1,2,3-trimethyl-benzene] 1.71 1.04 25.0 GC (SHSGC) É. Fenyvesi 2005
[a-Cyclodextrin](1).[1,2,4-trimethyl-benzene] 1.41 0.85 25.0 GC (SHSGC) É. Fenyvesi 2005
[a-Cyclodextrin](1).[D-phenylalanine] 0.90 0.78 5.01 25.0 Titration calorimetry Robert N. Goldberg 1994
[a-Cyclodextrin](1).[L-phenylalanineamide+] 1.08 0.04 5.01 25.0 Titration calorimetry Robert N. Goldberg 1994
[a-Cyclodextrin](1).[L-phenylalanineamide0] 1.27 0.36 10.02 25.0 Titration calorimetry Robert N. Goldberg 1994
[a-Cyclodextrin](1).[2-propanol] 0.99 0.49 6.9 25.0 Titration calorimetry Robert N. Goldberg 1994
[a-Cyclodextrin](1).[(S)-(+)-2-butanol] 1.38 0.34 6.9 25.0 Titration calorimetry Robert N. Goldberg 1994
[a-Cyclodextrin](1).[(R)-(-)-2-butanol] 1.39 0.11 6.9 25.0 Titration calorimetry Robert N. Goldberg 1994
[a-Cyclodextrin](1).[(+/-)-2-butanol] 1.44 0.18 6.9 25.0 Titration calorimetry Robert N. Goldberg 1994
[a-Cyclodextrin](1).[(S)-(+)-2-pentanol] 2.10 0.48 6.9 25.0 Titration calorimetry Robert N. Goldberg 1994
[a-Cyclodextrin](1).[(R)-(-)-2-pentanol] 2.10 0.60 6.9 25.0 Titration calorimetry Robert N. Goldberg 1994
[a-Cyclodextrin](1).[(S)-(+)-2-hexanol] 2.54 1.04 6.9 25.0 Titration calorimetry Robert N. Goldberg 1994
[a-Cyclodextrin](1).[(R)-(-)-2-hexanol] 2.54 1.23 6.9 25.0 Titration calorimetry Robert N. Goldberg 1994
[a-Cyclodextrin](1).[4,4’-bipyridine] 1.39 25.0 stopped-flow spectrophotometry R.Prado-Gotor 2006
[a-Cyclodextrin](1).[norflurazon] 1.71 0.20 25.0 HPLC, fluorescence spectroscopy Jaime Villaverde 2005
[a-Cyclodextrin](2).[2'-hydroxy-2-trans-styrylquinoline] 4.06 UV-Vis spectroscopy, fluorescence spectroscopy Shun-Li Wang 2005
[a-Cyclodextrin](2).[2'-methoxy-2-trans-styrylquinoline] 3.51 UV-Vis spectroscopy, fluorescence spectroscopy Shun-Li Wang 2005
[a-Cyclodextrin](1).[p-nitrophenolate ion] 3.27 1.30 10.4 25.0 UV and NMR spectroscopy Yoshihisa Matsui 1994
[a-Cyclodextrin](1).[p-nitrophenolate ion] 3.20 25.0 optical rotation method Yannis L. Loukas 1997
[a-Cyclodextrin](1).[p-nitrophenolate ion] 3.55 gel chromatography Yannis L. Loukas 1997
[a-Cyclodextrin](1).[I -] 0.96 -0.52 0.7 25.0 UV and NMR spectroscopy Yoshihisa Matsui 1994
[a-Cyclodextrin](1).[SCN-] 1.35 -0.52 0.7 25.0 UV and NMR spectroscopy Yoshihisa Matsui 1994
[a-Cyclodextrin](1).[ClO4-] 1.42 -0.40 0.7 25.0 UV and NMR spectroscopy Yoshihisa Matsui 1994
[a-Cyclodextrin](1).[simvastatin] 2.73 25.0 UV spectrophotometry Ziyang Liu 2005
[a-Cyclodextrin](1).[4-amino-phthalimide] 1.96 fluorescence spectroscopy Véronique Wintgens 2004
[a-Cyclodextrin](1).[Ponceau SX] 4.88 23.0 electrospray ionization mass spectrometry, Uv-vis and fluorescence spectroscopy Hanqi Zhang 2006
[a-Cyclodextrin](1).[Allura Red AC] 5.31 23.0 electrospray ionization mass spectrometry, Uv-vis and fluorescence spectroscopy Hanqi Zhang 2006
[a-Cyclodextrin](1).[Tartrazine] 4.13 23.0 electrospray ionization mass spectrometry, Uv-vis and fluorescence spectroscopy Hanqi Zhang 2006
[a-Cyclodextrin](1).[Orange II] 3.39 23.0 electrospray ionization mass spectrometry, Uv-vis and fluorescence spectroscopy Hanqi Zhang 2006
[a-Cyclodextrin](0.5).[Orange II] 6.34 23.0 electrospray ionization mass spectrometry, Uv-vis and fluorescence spectroscopy Hanqi Zhang 2006
[a-Cyclodextrin](1).[1,2,4 trithiolane] -2.57 25.0 gas chromatography-mass spectrometry, scanning electron microscopy Takeshi Furuta 2005
[a-Cyclodextrin](1).[1,2,4,5-tetrathiane] -2.36 25.0 gas chromatography-mass spectrometry, scanning electron microscopy Takeshi Furuta 2005
[a-Cyclodextrin](1).[1,2,3,4-tetrathiane] -2.45 25.0 gas chromatography-mass spectrometry, scanning electron microscopy Takeshi Furuta 2005
[a-Cyclodextrin](1).[1,2,3,5,6-pentathiepane] -2.28 25.0 gas chromatography-mass spectrometry, scanning electron microscopy Takeshi Furuta 2005
[a-Cyclodextrin](1).[hexathiepane] -4.52 25.0 gas chromatography-mass spectrometry, scanning electron microscopy Takeshi Furuta 2005
[a-Cyclodextrin](1).[L-histidine] 3.95 7.0 25.0 microcalorimetry Giuseppina Castronuovo 1995
[a-Cyclodextrin](1).[L-histidine] 4.08 11.3 25.0 microcalorimetry Giuseppina Castronuovo 1995
[a-Cyclodextrin](1).[11-Amino-undecanoic acid] 6.34 4.30 6.7 25.0 microcalorimetry Giuseppina Castronuovo 1995
[a-Cyclodextrin](1).[8-Amino-octanoic acid] 4.88 3.48 7.1 25.0 microcalorimetry Giuseppina Castronuovo 1995
[a-Cyclodextrin](1).[2-Amino-octanoic acid] 5.80 4.48 7.8 25.0 microcalorimetry Giuseppina Castronuovo 1995
[a-Cyclodextrin](1).[6-Aminohexanoic acid] 4.34 3.78 7.0 25.0 microcalorimetry Giuseppina Castronuovo 1995
[a-Cyclodextrin](1).[2-Aminohexanoic acid] 4.66 3.30 25.0 microcalorimetry Giuseppina Castronuovo 1995
[a-Cyclodextrin](1).[2-Aminopentanoic acid] 4.08 3.85 25.0 microcalorimetry Giuseppina Castronuovo 1995
[a-Cyclodextrin](1).[2,6-Diaminohexanoic acid] 3.70 3.30 10.0 25.0 microcalorimetry Giuseppina Castronuovo 1995
[a-Cyclodextrin](1).[2,6-Diaminohexanoic acid] 4.03 2.48 11.3 25.0 microcalorimetry Giuseppina Castronuovo 1995
[a-Cyclodextrin](1).[adamantane carboxylate] 2.00 10.0 25.0 UV-vis spectroscopy Rita H. de Rossi 1995
[a-Cyclodextrin](1).[butanoic acid] 4.93 4.15 11.3 25.0 calorimetry Giuseppina Castronuovo 1996
[a-Cyclodextrin](1).[octanoic acid (bent form)] 6.13 5.05 11.3 25.0 calorimetry Giuseppina Castronuovo 1996
[a-Cyclodextrin](1).[nonanoic acid (bent form)] 5.40 4.30 11.3 25.0 calorimetry Giuseppina Castronuovo 1996
[a-Cyclodextrin](1).[decanoic acid (bent form)] 5.40 3.78 11.3 25.0 calorimetry Giuseppina Castronuovo 1996
[a-Cyclodextrin](1).[undecanoic acid] 5.93 4.23 11.3 25.0 calorimetry Giuseppina Castronuovo 1996
[a-Cyclodextrin](1).[calcichrome] 2.76 2.11 25.0 NMR spectroscopy Bo-Long Poh 1996
[a-Cyclodextrin](1).[m-nitrophenol] 2.64 1.78 11.0 25.0 capillary electrophoresis Daniel W. Armstrong 1996
[a-Cyclodextrin](1).[m-nitrophenol] 2.31 0.48 11.1 25.0 calorimetry Daniel W. Armstrong 1996
[a-Cyclodextrin](1).[3-cyanophenol] 2.04 1.48 3.05 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[a-Cyclodextrin](1).[3-cyanophenolate ion] 2.56 10.28 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[a-Cyclodextrin](1).[4-cyanophenol] 2.08 1.30 3.05 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[a-Cyclodextrin](1).[4-cyanophenolate] 2.76 1.70 10.28 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[a-Cyclodextrin](1).[4-cyanophenolate] 2.80 10.3 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[a-Cyclodextrin](1).[3-nitrophenol] 2.15 1.78 3.5 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[a-Cyclodextrin](1).[3-nitrophenolate ion] 2.48 1.60 10.28 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[a-Cyclodextrin](1).[4-nitrophenol] 2.23 1.30 3.5 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[a-Cyclodextrin](1).[4-nitrophenolate ion] 3.28 1.90 10.28 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[a-Cyclodextrin](1).[4-bromophenol] 2.40 1.48 3.5 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[a-Cyclodextrin](1).[4-bromophenolate ion] 2.98 10.28 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[a-Cyclodextrin](1).[4-methoxyphenol] 1.52 1.00 4.0 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[a-Cyclodextrin](1).[4-methoxyphenolate ion] 1.49 10.6 25.0 absorption spectroscopy, NMR Sanyo Hamai 1997
[a-Cyclodextrin](1).[p-nitrophenyl isonicotinate] 2.04 9.5 25.0 NMR spectroscopy Paolo Scrimin 1997
[a-Cyclodextrin](1).[p-nitrophenyl nicotinate] 1.95 9.5 25.0 NMR spectroscopy Paolo Scrimin 1997
[a-Cyclodextrin](1).[p-nitrophenyl urocanoate] 1.95 10.5 25.0 NMR spectroscopy Paolo Scrimin 1997
[a-Cyclodextrin](1).[m-nitrophenyl isonicotinate] 1.95 9.5 25.0 NMR spectroscopy Paolo Scrimin 1997
[a-Cyclodextrin](1).[mono-substitued benzene, H] 1.46 0.15 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[mono-substitued benzene, H] 1.50 Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[methylbenzene] 1.56 0.43 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[methylbenzene] 1.52 0.48 25.0 Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[ethylbenzene] 2.02 0.85 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[ethylbenzene] 2.04 1.00 25.0 Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[mono-substitued benzene, C2H] 1.94 1.63 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[mono-substitued benzene, OCH3] 2.15 0.85 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[mono-substitued benzene, OC2H5] 2.23 0.90 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[mono-substitued benzene, CH2OH] 1.98 0.63 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[mono-substitued benzene, CH2Cl] 2.31 1.04 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[mono-substitued benzene, CHO] 2.01 0.60 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[mono-substitued benzene, COCH3] 2.15 0.78 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[mono-substitued benzene, COOCH3] 2.33 1.00 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[mono-substitued benzene, COOC2H5] 2.56 1.11 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[cyanobenzene] 1.89 1.11 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[aminobenzene] 1.16 0.04 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[aminobenzene] 0.94 -0.92 Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[mono-substitued benzene, NHCH3] 1.92 0.40 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[mono-substitued benzene, NHC2H5] 2.11 0.70 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[mono-substitued benzene, N(CH3)2] 2.24 0.90 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[mono-substitued benzene, NHCOCH3] 2.01 0.60 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[nitrobenzene] 1.95 0.68 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[nitrobenzene] 1.69 1.00 Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[fluorobenzene] 1.60 0.20 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[fluorobenzene] 1.53 25.0 Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[chlorobenzene] 2.05 1.00 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[chlorobenzene] 2.00 1.00 25.0 Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[bromobenzene] 2.73 1.23 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[bromobenzene] 2.71 1.00 25.0 Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[iodobenzene] 3.08 1.30 25.0 Uv-vis and fluorescence spectroscopy Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[iodobenzene] 3.04 1.00 25.0 Qing-Xiang Guo 1998
[a-Cyclodextrin](1).[calcium acetylhomotaurinate] 0.66 -0.40 40.0 NMR spectroscopy Irina N. Topchieva 1998
[a-Cyclodextrin](1).[calcium acetylhomotaurinate] 0.48 -0.70 50.0 NMR spectroscopy Irina N. Topchieva 1998
[a-Cyclodextrin](1).[calcium acetylhomotaurinate] 0.32 -0.70 60.0 NMR spectroscopy Irina N. Topchieva 1998
[a-Cyclodextrin](1).[cetyltrimethylammonium bromide] 5.00 isothermal titration calorimetry E. Wyn-Jones 1995
[a-Cyclodextrin](2).[cetyltrimethylammonium bromide] 4.31 isothermal titration calorimetry E. Wyn-Jones 1995
[a-Cyclodextrin](1).[n-butyl group on polymer chain] 1.74 NMR spectroscopy Akira Harada 1997
[a-Cyclodextrin](1).[isobutyl group on polymer chain] 1.56 NMR spectroscopy Akira Harada 1997
[a-Cyclodextrin](1).[n-hexyl group on polymer chain] 2.46 NMR spectroscopy Akira Harada 1997
[a-Cyclodextrin](1).[isooctyl group on polymer chain] 2.48 NMR spectroscopy Akira Harada 1997
[a-Cyclodextrin](1).[dodecyl group on polymer chain] 3.00 NMR spectroscopy Akira Harada 1997
[a-Cyclodextrin](1).[n-butanol] 1.30 NMR spectroscopy Akira Harada 1997
[a-Cyclodextrin](1).[tert-butyl alcohol on polymer chain] 0.78 NMR spectroscopy Akira Harada 1997
[a-Cyclodextrin](1).[riboflavin 5'-(dihydrogen phosphate) monosodium salt] 3.22 2.19 fluorescence spectroscopy Yannis L. Loukas 1997
[a-Cyclodextrin](2).[riboflavin 5'-(dihydrogen phosphate) monosodium salt] 2.54 1.64 fluorescence spectroscopy Yannis L. Loukas 1997
[a-Cyclodextrin](1).[warfarin] 1.58 9.5 25.0 fluorescence spectroscopy Mamoru Kamiya 1997
[a-Cyclodextrin](1).[m-nitro-phenylacetate] 1.61 7.0 25.0 spectophotometry Yoshihiro Taniguchi 1982
[a-Cyclodextrin](1).[m-methyl-phenylacetate] 1.69 8.3 25.0 spectophotometry Yoshihiro Taniguchi 1982
[a-Cyclodextrin](1).[p-methyl-phenylacetate] 1.93 9.0 25.0 spectophotometry Yoshihiro Taniguchi 1982
[a-Cyclodextrin](1).[dimethyl isophthalate] 2.20 25.0 fluorescence spectroscopy Francisco Mendicuti 2004
[a-Cyclodextrin](1).[dimethyl isophthalate] 2.31 1.36 5.0 fluorescence spectroscopy Francisco Mendicuti 2004
[a-Cyclodextrin](1).[dimethyl isophthalate] 2.19 1.49 15.0 fluorescence spectroscopy Francisco Mendicuti 2004
[a-Cyclodextrin](1).[dimethyl isophthalate] 2.12 1.60 35.0 fluorescence spectroscopy Francisco Mendicuti 2004
[a-Cyclodextrin](1).[dimethyl isophthalate] 2.01 0.70 45.0 fluorescence spectroscopy Francisco Mendicuti 2004
[a-Cyclodextrin](1).[prednisolone] 2.46 0.85 5.5 25.0 NMR spectroscopy Kim L.Larsen 2005
[a-Cyclodextrin](1).[prednisolone] 2.47 25.0 NMR, UV-vis spectroscopy, X-ray diffraction Kim L.Larsen 2005
[a-Cyclodextrin](1).[6a-methyl prednisolone] 1.99 0.48 5.5 25.0 NMR spectroscopy Kim L.Larsen 2005
[a-Cyclodextrin](1).[acetone] 0.47 -1.28 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[butan-2-one] 0.99 -0.42 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[pentan-2-one] 1.59 0.13 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[hexan-2-one] 2.12 0.20 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[heptan-2-one] 2.55 0.71 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[octan-2-one] 3.01 1.97 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[pentan-3-one] 1.30 -0.28 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[hexan-3-one] 1.79 0.05 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[heptan-3-one] 2.22 0.44 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[octan-3-one] 2.59 1.32 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[cyclobutanone] 0.86 -0.80 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[cyclopentanone] 1.12 -0.75 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[cyclohexanone] 1.16 -0.14 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[cycloheptanone] 1.14 -0.19 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[cyclooctanone] 1.32 -0.12 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[3-methylbutan-2-one] 0.91 -0.70 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[3-methylpentan-2-one] 1.55 -0.13 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[5-methylhexan-2-one] 1.71 0.03 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[3,3-dimethylbutan-2-one] 0.98 -0.44 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[4-methylpentan-2-one] 1.27 -0.15 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[heptan-4-one] 2.04 0.60 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[acetophenone] 1.10 -0.28 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[heptan-2-ol] 2.97 1.54 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[hexan-3-ol] 2.22 0.35 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[heptan-3-ol] 2.59 0.66 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[octan-3-ol] 3.08 1.35 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[1-phenylethanol] 1.12 -0.31 11.6 25.0 inhibition kinetics method, stopped-flow spectroscopy Oswald S.Tee 1996
[a-Cyclodextrin](1).[barbital] 1.97 0.95 10.0 freezing point depression method Masahiko Suzuki 1993
[a-Cyclodextrin](1).[barbital] 1.92 UV spectroscopy Masahiko Suzuki 1993
[a-Cyclodextrin](1).[phenobarbital] 1.30 8.7 freezing point depression method Masahiko Suzuki 1993
[a-Cyclodextrin](1).[phenobarbital] 1.30 UV spectroscopy Masahiko Suzuki 1993
[a-Cyclodextrin](1).[pentobarbital] 2.72 1.52 9.9 freezing point depression method Masahiko Suzuki 1993
[a-Cyclodextrin](1).[pentobarbital] 2.64 UV spectroscopy Masahiko Suzuki 1993
[a-Cyclodextrin](2).[barbital] 0.98 0.32 10.0 freezing point depression method Masahiko Suzuki 1993
[a-Cyclodextrin](2).[barbital] 0.96 UV spectroscopy Masahiko Suzuki 1993
[a-Cyclodextrin](2).[phenobarbital] 0.69 -0.52 8.7 freezing point depression method Masahiko Suzuki 1993
[a-Cyclodextrin](2).[phenobarbital] 0.83 UV spectroscopy Masahiko Suzuki 1993
[a-Cyclodextrin](2).[pentobarbital] 1.64 0.90 9.9 freezing point depression method Masahiko Suzuki 1993
[a-Cyclodextrin](2).[pentobarbital] 1.62 UV spectroscopy Masahiko Suzuki 1993
[a-Cyclodextrin](1).[isopropyl p-nitrophenyl methylphosphonate; R(-)enantiomer] -0.40 -1.49 12.0 25.0 spectrophotometry C.van Hooidonk 1970
[a-Cyclodextrin](1).[isopropyl p-nitrophenyl methylphosphonate; R(-)enantiomer] -0.46 -1.32 12.3 25.0 spectrophotometry C.van Hooidonk 1970
[a-Cyclodextrin](1).[isopropyl p-nitrophenyl methylphosphonate; R(-)enantiomer] -0.51 -1.11 12.6 25.0 spectrophotometry C.van Hooidonk 1970
[a-Cyclodextrin](1).[isopropyl p-nitrophenyl methylphosphonate; R(-)enantiomer] -0.54 -1.61 12.8 25.0 spectrophotometry C.van Hooidonk 1970
[a-Cyclodextrin](1).[isopropyl p-nitrophenyl methylphosphonate; R(-)enantiomer] -0.59 -0.86 12.9 25.0 spectrophotometry C.van Hooidonk 1970
[a-Cyclodextrin](1).[formic acid] 0.65 -0.05 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[a-Cyclodextrin](1).[oxalic acid] 1.45 0.52 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[a-Cyclodextrin](1).[malic acid] 0.59 0.23 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[a-Cyclodextrin](1).[tartaric acid] 0.18 -0.52 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[a-Cyclodextrin](1).[maleic acid] 1.09 0.18 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[a-Cyclodextrin](1).[citric acid] 1.12 0.61 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[a-Cyclodextrin](1).[iodid ion] 1.62 1.08 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[a-Cyclodextrin](1).[nitrate ion (NO3-)] 0.91 0.23 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[a-Cyclodextrin](1).[perchlorate ion (ClO4-)] 1.92 1.05 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[a-Cyclodextrin](1).[fulminate ion (CNO-)] 0.67 0.41 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[a-Cyclodextrin](1).[thiocianate/rodanid ion (SCN-)] 1.80 1.18 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[a-Cyclodextrin](1).[dichromate ion(Cr2O72-)] 1.51 0.65 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[a-Cyclodextrin](1).[L-leucine] 0.94 -0.30 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[a-Cyclodextrin](1).[L-isoleucine] 0.92 -0.30 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[a-Cyclodextrin](1).[L-methionine] 1.24 -0.52 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[a-Cyclodextrin](1).[L-tryptophane] 1.44 -0.22 freezing point depression method, osmotic measurements Masahiko Suzuki 1993
[a-Cyclodextrin](1).[benzoate ion] 1.20 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[benzoate ion] 1.11 25.0 spectrophotometry Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[benzoate ion] 1.00 25.0 microcalorimetry Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[benzoate ion] 1.05 -0.46 25.0 potentiometry Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[2-methyl benzoate ion] 1.11 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[3-methyl benzoate ion] 1.41 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[4-methyl benzoate ion] 1.56 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[2,4-dimethyl benzoate ion] 1.65 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[2,5-dimethyl benzoate ion] 1.61 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[3,5-dimethyl benzoate ion] 1.59 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[3,5-dimethoxy benzoate ion] 1.67 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[salicylate ion] 1.04 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[salicylate ion] 0.90 -0.52 25.0 capillary electrophoresis(IAD) Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[salicylate ion] 1.18 0.78 25.0 capillary electrophoresis(DAD) Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[3-phenyl propionate ion] 1.54 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[4-tert-butyl benzoate ion] 1.71 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[4-tert-butyl benzoate ion] 1.81 1.28 25.0 potentiometry Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[ibuprofen anion] 1.75 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[1-adamantane carboxylate ion] 2.06 25.0 capillary electrophoresis Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[1-adamantane carboxylate ion] 2.15 1.15 25.0 spectrophotometry Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[1-adamantane carboxylate ion] 2.15 25.0 microcalorimetry Wolfgang Zimmermann 1998
[a-Cyclodextrin](1).[4-(N,N-dimethylamino)benzonitrile] -0.28 -2.00 25.0 fluorescence spectroscopy Edwin Quinones 1999
[a-Cyclodextrin](2).[gentian violet] 4.34 3.30 21.0 UV-vis spectroscopy David Díaz 1999
[a-Cyclodextrin](1).[gentian violet] 2.29 0.85 7.5 25.0 UV-vis spectroscopy David Díaz 1999
[a-Cyclodextrin](1).[gentian violet] 2.05 0.70 25.0 UV-vis spectroscopy David Díaz 1999
[a-Cyclodextrin](1).[7-ferrocenyl-2,4,6-heptatrienal] 2.90 1.30 25.0 spectrophotometry Angel E. Kaifer 2000
[a-Cyclodextrin](1).[7-ferrocenyl-2,4,6-heptatrienol] 3.36 2.11 25.0 spectrophotometry Angel E. Kaifer 2000
[a-Cyclodextrin](1).[N-dodecyl-N'-(2-phosphonoethyl)-1,4,5,8-naphthalenetetracarboxylic diimide] 2.05 9.0 25.0 UV-vis spectroscopy Sergio Brochsztain 2005
[a-Cyclodextrin](1).[N,N'-bis(butyl)-1,4,5,8-naphthalenetetracarboxylic diimide] 3.12 Sergio Brochsztain 2005
[a-Cyclodextrin](1).[PGE1] 3.09 2.57 25.0 conductometry Tore Ramstad 2005
[a-Cyclodextrin](1).[PGE1] 2.59 27.0 NMR spectroscopy Tore Ramstad 2005
[a-Cyclodextrin](1).[PGE1] 2.87 1.78 27.0 conductometry Tore Ramstad 2005
[a-Cyclodextrin](1).[PGE1] 2.79 1.81 30.0 conductometry Tore Ramstad 2005
[a-Cyclodextrin](1).[PGE1] 2.74 1.72 37.0 conductometry Tore Ramstad 2005
[a-Cyclodextrin](1).[PGE1] 2.85 1.81 7.2 27.0 capillary electrophoresis Tore Ramstad 2005
[a-Cyclodextrin](1).[PGE1] 2.81 1.71 7.2 30.0 capillary electrophoresis Tore Ramstad 2005
[a-Cyclodextrin](1).[PGE1] 2.73 1.43 7.2 37.0 capillary electrophoresis Tore Ramstad 2005
[a-Cyclodextrin](2).[1-adamantane carboxylate] 2.15 25.0 pH titration Marcin Majda 2000
[a-Cyclodextrin](1).[alkyl-substitued hydroxyphenylazo derivative of sulfanilic acid; acid form] 3.80 4.6 25.0 Uv-vis absorption spectroscopy, circular dichroism Noboru Yoshida 1990
[a-Cyclodextrin](1).[alkyl-substitued hydroxyphenylazo derivative of sulfanilic acid; based form] 3.77 12.0 25.0 Uv-vis absorption spectroscopy, circular dichroism Noboru Yoshida 1990
[a-Cyclodextrin](1).[adamantanecarboxylic acid] 2.15 8.5 25.0 microcalorimetry Maurice R. Eftink 1985
[a-Cyclodextrin](1).[adamantanecarboxylic acid] 2.11 4.08 25.0 microcalorimetry Maurice R. Eftink 1985
[a-Cyclodextrin](1).[adamantanecarboxylic acid] 2.36 7.2 25.0 microcalorimetry Maurice R. Eftink 1985
[a-Cyclodextrin](1).[adamantanecarboxylic acid] 2.18 4.5 25.0 pH potentiometry Maurice R. Eftink 1985
[a-Cyclodextrin](2).[adamantanecarboxylate] 1.00 4.08 25.0 microcalorimetry Maurice R. Eftink 1985
[a-Cyclodextrin](2).[adamantanecarboxylate] 1.08 4.5 25.0 pH potentiometry Maurice R. Eftink 1985
[a-Cyclodextrin](2).[adamantanecarboxylic acid] 2.78 4.5 25.0 pH potentiometry Maurice R. Eftink 1985
[a-Cyclodextrin](2).[adamantanecarboxylic acid] 2.70 4.08 25.0 microcalorimetry, pH potentiometry Maurice R. Eftink 1985
[a-Cyclodextrin].[pullulanase] 4.11 UV difference spectroscopy, flow calorimetry Bent W. Sigurskjold 1994