NMR spectroscopic characterization of inclusion complexes comprising cyclodextrins and gallated catechins in aqueous solution : cavity size dependency

Copyright (c) 2008 John Wiley & Sons, Ltd

Bibliographische Detailangaben
Veröffentlicht in:Magnetic resonance in chemistry : MRC. - 1985. - 47(2009), 4 vom: 05. Apr., Seite 283-7
1. Verfasser: Ishizu, Takashi (VerfasserIn)
Weitere Verfasser: Tsutsumi, Hiroyuki, Yamamoto, Hideji, Harano, Kazunobu
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2009
Zugriff auf das übergeordnete Werk:Magnetic resonance in chemistry : MRC
Schlagworte:Journal Article Solutions gamma-Cyclodextrins gallocatechin gallate 0C056HB16M Catechin 8R1V1STN48 epigallocatechin gallate BQM438CTEL Deuterium Oxide mehr... J65BV539M3 gamma-cyclodextrin KZJ0BYZ5VA
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520 |a The structure of inclusion complexes of gamma-cyclodextrin (gamma-CD), (-)-gallocatechin gallate (GCg), and (-)-epigallocatechin gallate (EGCg) in D(2)O was investigated using several NMR techniques. GCg formed a 1:1 inclusion complex with gamma-CD in which the A and C rings of GCg were inserted deep at the head of the A ring into the gamma-CD cavity from the wide secondary hydroxyl group side. In the 1:1 inclusion complex with GCg and gamma-CD, the GCg moiety maintained a conformation in which the B and B' rings of GCg took both pseudoequatorial positions with respect to the C ring. The structure of the inclusion complex of GCg and gamma-CD obtained from NMR experiments supported well that determined from PM6 semiempirical SCF MO calculations. However, (1)H NMR experiments suggested that EGCg did not form any inclusion complex with gamma-CD in D(2)O. The marked difference between GCg and EGCg in inclusion behavior toward gamma-CD may be explained in terms of the stabilization energy calculated with the PM6 method. 
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700 1 |a Tsutsumi, Hiroyuki  |e verfasserin  |4 aut 
700 1 |a Yamamoto, Hideji  |e verfasserin  |4 aut 
700 1 |a Harano, Kazunobu  |e verfasserin  |4 aut 
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