Kinetic isotope H/D effect in the oxidation of ethers of linoleic acid in solutions
- Authors: Tikhonov I.V.1, Moskalenko I.V.1, Pliss E.M.1, Fomich M.A.2, Bekish A.V.3, Shmanai V.V.2
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Affiliations:
- Demidov Yaroslavl University
- Institute of Physical Organic Chemistry
- Belarus State University
- Issue: Vol 11, No 3 (2017)
- Pages: 395-399
- Section: Kinetics and Mechanism of Chemical Reactions. Catalysis
- URL: https://journal-vniispk.ru/1990-7931/article/view/199177
- DOI: https://doi.org/10.1134/S1990793117030113
- ID: 199177
Cite item
Abstract
It is shown that the initiated oxidation of deuterated esters of linoleic acid proceeds as a radical chain process. The value of the kinetic isotope effect for hydrogen atom abstraction from the bisallyl group of linoleic acid esters is determined: 3.0 for tert-butyl peroxy and cumylperoxy radicals.
About the authors
I. V. Tikhonov
Demidov Yaroslavl University
Email: e.pliss@mail.ru
Russian Federation, Yaroslavl, 150000
I. V. Moskalenko
Demidov Yaroslavl University
Email: e.pliss@mail.ru
Russian Federation, Yaroslavl, 150000
E. M. Pliss
Demidov Yaroslavl University
Author for correspondence.
Email: e.pliss@mail.ru
Russian Federation, Yaroslavl, 150000
M. A. Fomich
Institute of Physical Organic Chemistry
Email: e.pliss@mail.ru
Belarus, Minsk, 220072
A. V. Bekish
Belarus State University
Email: e.pliss@mail.ru
Belarus, Minsk, 220030
V. V. Shmanai
Institute of Physical Organic Chemistry
Email: e.pliss@mail.ru
Belarus, Minsk, 220072
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