Reaction of 3,4,6-Triisopropyl-о-benzoquinone with 3,4,6-Triisopropylcatechol
- Authors: Kurskii Y.A.1, Shavyrin A.S.1, Kulikova T.I.1, Kuropatov V.A.1, Abakumov G.A.1
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Affiliations:
- G.A. Razuvaev Institute of Organometallic Chemistry
- Issue: Vol 88, No 8 (2018)
- Pages: 1584-1589
- Section: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/222351
- DOI: https://doi.org/10.1134/S1070363218080054
- ID: 222351
Cite item
Abstract
Formation of protonated 3,4,6-triisopropylsemiquinone radicals in solution of a mixture of 3,4,6- triisopropyl-о-benzoquinone and 3,4,6-triisopropylcatechol was shown using ESR spectroscopy. Heating the mixture to 110°С leads to the formation of the condensation products, additional amount of 3,4,6-triisopropylcatechol, and evolution of propylene. Mathematical simulation of the kinetics of the reaction was performed.
Keywords
About the authors
Yu. A. Kurskii
G.A. Razuvaev Institute of Organometallic Chemistry
Author for correspondence.
Email: kursk@iomc.ras.ru
Russian Federation, ul. Tropinina 49, Nizhny Novgorod, 603950
A. S. Shavyrin
G.A. Razuvaev Institute of Organometallic Chemistry
Email: kursk@iomc.ras.ru
Russian Federation, ul. Tropinina 49, Nizhny Novgorod, 603950
T. I. Kulikova
G.A. Razuvaev Institute of Organometallic Chemistry
Email: kursk@iomc.ras.ru
Russian Federation, ul. Tropinina 49, Nizhny Novgorod, 603950
V. A. Kuropatov
G.A. Razuvaev Institute of Organometallic Chemistry
Email: kursk@iomc.ras.ru
Russian Federation, ul. Tropinina 49, Nizhny Novgorod, 603950
G. A. Abakumov
G.A. Razuvaev Institute of Organometallic Chemistry
Email: kursk@iomc.ras.ru
Russian Federation, ul. Tropinina 49, Nizhny Novgorod, 603950