Hp. Hendrickson et al., ELECTROCHEMISTRY OF CATECHOL-CONTAINING FLAVONOIDS, Journal of pharmaceutical and biomedical analysis, 12(3), 1994, pp. 325-334
The electrochemical properties of four structurally related flavonoids
, quercetin, quercetin-3-O-rhamnose (quercitrin), quercetin-3-O-rutino
se (rutin) and luteolin were investigated. These flavonoids were shown
to undergo homogenous chemical reactions following oxidation at a gla
ssy carbon electrode. These reactions were studied using cyclic voltam
metry and rotating ring-disk voltammetry. Both first-order and zero-or
der processes were observed. The rate of the zero-order process was st
rongly dependent on the substituent at the C-3 position of the flavono
id. The rate of the first-order process was independent of substitutio
n. Two products were observed using liquid chromatography. These produ
cts did not correspond to previously reported products of enzymatic ox
idation. The products were not stable under conditions for isolation.