Photoreduction of 3,6-Di-tert-Butyl-o-Benzoquinones in the Presence of N,N-Dimethylanilines in Binary Solvent Mixtures


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The effect of the composition and dielectric characteristics of binary solvent mixtures on the photoreduction rate constant (kH) of 3,6-di-tert-butyl-o-benzoquinone and its 4-cyano derivative in the presence of three N,N-dimethylanilines has been studied. It has been found that for the pair 3,6-di-tert-butyl-o-benzoquinone–N,N-dimethylaniline, the free energy electron transfer of which is ΔGe = +0.11 eV, ln kH is proportional to the difference of the reciprocals of experimentally determined optical and static permittivities for the toluene–acetonitrile and benzene–N,N-dimethylformamide blends. For quinone–amine pairs, which have ΔGe ≠ +0.11 eV, kH is maximal in toluene and benzene and decreases with the increasing amount of the polar component in the solvent mixture, with lnkH being inversely proportional to the permittivity of the medium.

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M. Shurygina

Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences

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Email: sch@iomc.ras.ru
俄罗斯联邦, Nizhny Novgorod, 603950

S. Chesnokov

Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences

Email: sch@iomc.ras.ru
俄罗斯联邦, Nizhny Novgorod, 603950

G. Abakumov

Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences

Email: sch@iomc.ras.ru
俄罗斯联邦, Nizhny Novgorod, 603950

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