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.
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Original Russian Text © V.I. Porkhun, E.V. Porkhun, D.N. Gurulev, L.V. Palatkina, 2018, published in Zhurnal Obshchei Khimii, 2018, Vol. 88, No. 8, pp. 1258–1261.
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Porkhun, V.I., Porkhun, E.V., Gurulev, D.N. et al. Elementary Stages of Photochemical Reactions of Substituted 2,6-Diphenyl-para-benzoquinones with Thiols. Russ J Gen Chem 88, 1580–1583 (2018). https://doi.org/10.1134/S1070363218080042
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DOI: https://doi.org/10.1134/S1070363218080042