
TY  - JOUR
A1  - Kennedy, JA 
A1  - Munro, MHG 
A1  - Powell, HKJ 
A1  - Porter, LJ 
A1  - Foo, LY 
T1  - The protonation reactions of catechin, epicatechin and related compounds
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1984
VL  - 37
IS  - 4
SP  - 885
EP  - 892
KW  - 
UR  - https://doi.org/10.1071/CH9840885 
N2  - The protonation reactions for catechin and epicatechin have been studied at 25ºC, I 0.10M (KCl). Equilibrium constants Kn for the protonation steps of the anions L4- have been determined from potentiometric and/or spectrophotometric measurements. The logKn values for the epimers differed significantly only for logKl and logK4 (values for catechin 13.26 ± 0.05, 11.26 ± 0.06, 9.41 ± 0.02, 8.64 ± 0.01, and epicatechin 13.40 ± 0.05, ll.23 ± 0.06, 9.49 ± 0.02, 8.72 ± .01, n = 1-4 respectively). These differences are ascribed to specific solvation effects or ion associations between K+ and the ligand anions. Epimerization was studied by h.p.l.c., and was found to be minimal over the experimental time scale at pH c. 13.5. The ring on which each stepwise protonation occurs was elucidated by reference to log Kn values measured for the model compounds catechol, 4-methylbenzene-1,2-diol, protocatechuic acid and 3',4'-di-O-methylcatechin. The protonation sequence is B ring, A ring, B ring and A ring. In contrast to earlier results, it has been established that the epimerization of catechin or epicatechin at C2, and the formation of catechinic acid in basic solution, may proceed through a radical rather than ionic mechanism. 
ER  -

