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Structure of a Beta-cyclodextrin-vanillin inclusion complex.

Divakar, S. (1990) Structure of a Beta-cyclodextrin-vanillin inclusion complex. Journal of Agricultural and Food Chemistry, 38 (4). pp. 940-944.

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Abstract

Vanillin was found to form a stable complex with 0-cyclodextrin. A binding constant value of 1.11 X lo4 M-' was determined for the 1:l complex. 'H NMR chemical shift differences and circular dichroism spectra indicated that both phenolic end and aldehyde end were affected by complexation. 2D nuclear Overhauser enhancement spectroscopy indicated proximity of OCH, in vanillin to the anomeric protons of P-cyclodextrin. 1D difference NOE experiments have revealed that vanillin exists with the phenolic end nearer to the narrower end and the aldehyde end to the wider end of the torusshaped 0-cyclodextrin molecule.

Item Type: Article
Uncontrolled Keywords: Vanillin, beta-cyclodextrin, NMR study, BCD complexes
Subjects: 500 Natural Sciences and Mathematics > 04 Chemistry and Allied Sciences > 24 Organic Chemistry
Divisions: Dept. of Biochemistry
Depositing User: Food Sci. & Technol. Information Services
Date Deposited: 05 Mar 2018 08:18
Last Modified: 05 Mar 2018 08:18
URI: http://ir.cftri.com/id/eprint/5537

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