Kinetic isotope H/D effect in the oxidation of ethers of linoleic acid in solutions


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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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