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Title: ESR spectra and kinetics of the disproportionation of substituted phenoxyl radicals. III. Cross-disproportionation in a system containing two phenols

Journal Article · · Kinet. Catal. (Engl. Transl.); (United States)
OSTI ID:5251432

An ESR method was used to study the kinetics of radical reactions in systems of an initiator with two phenolic antioxidants. A theoretical analysis yielded formulas for calculating the equilibrium constant of reversible phenol-phenoxyl exchange reactions and the rate constant for the cross-disproportionation of phenoxyl radicals. Equilibrium and cross-disproportionation constants were measured for five different binary systems. From the results it was concluded that a connection exists between the cross-disproportionation rate constant and the structure of the phenol (in this case steric factors are most important than the O-H bond strength in the phenol). It is shown that the cross-disproportionation of phenoxyl radicals may lead to the generation of a more active antioxidant, as in the case of ionol + a synthetic analog of ..cap alpha..-tocopherol, leading to synergistic effects.

Research Organization:
Institute of Chemical Physics, Moscow (USSR)
OSTI ID:
5251432
Journal Information:
Kinet. Catal. (Engl. Transl.); (United States), Vol. 28:2; Other Information: Translated from Kinet. Katal.; 28: No. 2, 305-312(Mar-Apr 1987)
Country of Publication:
United States
Language:
English