Elementary Stages of Photochemical Reactions of Substituted 2,6-Diphenyl-para-benzoquinones with Thiols


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Abstract

Using the effects of chemical polarization of nuclei, mechanism and elementary stages of photochemical reduction of 2,6-diphenyl-1,4-benzoquinone with thiols have been elucidated. The studied quinone is reduced with ethanethiol in two stages (transfer of electron followed by proton transfer). The final photolysis product is a derivative of dibenzofuran.

About the authors

V. I. Porkhun

Volgograd State Technical University

Email: lv.palatkina@yandex.ru
Russian Federation, pr. Lenina 28, Volgograd, 400005

E. V. Porkhun

Volgograd State Technical University

Email: lv.palatkina@yandex.ru
Russian Federation, pr. Lenina 28, Volgograd, 400005

D. N. Gurulev

Volgograd State Technical University

Email: lv.palatkina@yandex.ru
Russian Federation, pr. Lenina 28, Volgograd, 400005

L. V. Palatkina

Volgograd State Technical University

Author for correspondence.
Email: lv.palatkina@yandex.ru
Russian Federation, pr. Lenina 28, Volgograd, 400005


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