M. Noferi et al., ANTIOXIDANT CHARACTERISTICS OF HYDROLYZABLE AND POLYFLAVONOID TANNINS- AN ESR KINETICS STUDY, Journal of applied polymer science, 63(4), 1997, pp. 475-482
As part of an investigation of the role of tannin as antioxidants, the
radical formation and radical decay reactions of some polyflavonoid a
nd hydrolysable tannins has been followed by electron spin resonance (
ESR) techniques. Comparative kinetics were determined for both light-i
nduced radicals and by radical transfer from a less stable chemical sp
ecies for the tannin alone and when the tannin is in a methanol soluti
on. The five parameters which appear to have a bearing on the very com
plex pattern of the rates of tannin radical formation and radical deca
y were found to be (1) the extent of the colloidal state of the tannin
in solution, (2) the stereochemical structure at the interflavonoid u
nits linkage, (3) the ease of heterocyclic pyran ring opening, (4) the
relative numbers of A- and B-rings hydroxy groups, and (5) solvation
effects when the tannin is in solution. It is the combination of these
five factors that appears to determine the behavior as an antioxidant
of a particular tannin under a set of application conditions. (C) 199
7 John Wiley & Sons, Inc.