Kinetics of the reaction between the antioxidant Trolox and the free radical DPPH in semi-aqueous solution.

Reaction of the free-radical diphenylpicrylhydrazyl (DPPH(.)) with Trolox (TrOH) was investigated in buffered hydroalcoholic media by using a stopped-flow system. DPPH was reduced to the hydrazine analogue DPPH-H with a measured stoichiometry of about 2. DPPH-H was characterized by an acid-base equilibrium (pKa = 8.6). Time-resolved absorption spectra recorded with an excess of either TrOH or DPPH indicated that no significant amount of the TrO radical was accumulated. The TrO radical formed in a first step further reacted quickly with DPPH(.). For 1 : 1 ethanol-buffer mixtures at pH 7.4, the bimolecular rate constants of the first and second steps were 1.1 x 10(4) M(-1) s(-1) and 2 x 10(6) M(-1) s(-1), respectively. A significant increase of the measured rate constant was observed for ethanol-buffer solutions as compared to ethanol. The rate was also increased at higher pH. A deuterium isotopic effect of 2.9 was measured. These data are discussed with regards to mechanisms involving either electron or proton exchange as rate determining steps in the reaction of DPPH with Trolox. The importance of solvent acidity control in investigation of antioxidant properties is outlined.