Issue 43, 2021

A computational study of the reaction mechanism of 2,2-azobis(isobutyronitrile)-initiated oxidative cleavage of geminal alkenes

Abstract

A computational study of 2,2-azobis(isobutyronitrile) (AIBN)-initiated aerobic oxidative cleavage of alkenes is carried out employing density functional theory (DFT) and high-level coupled-cluster methods, such as coupled-cluster singles and doubles with perturbative triples [CCSD(T)]. Our computations show that the barriers for the formation of dioxetane derivatives suggested by Xu and co-workers (J. Org. Chem., 2014, 79, 7220–7225) for the reaction mechanism of aerobic oxidative cleavage of alkenes are computed to be higher than 65 kcal mol−1. This barrier is relatively high under the reaction conditions. Our results for the Xu mechanism indicate that the reaction does not proceed via the formation of a dioxetane ring under the reaction conditions. Our results demonstrate that the reaction of aerobic oxidative cleavage of geminal alkenes in the presence of AIBN is initiated by the peroxyl radical 9, contrary to the isobutyronitrile radical 2. Our results show that the 2-(2-hydroxyl-1,1-diarylethoxy)-2-methylpropanenitrile radical (15) does not appear throughout the reaction scheme and the reaction progresses over the 2-(2-hydroxyl-2,2-diarylethoxy)-2-methylpropanenitrile radical (13) rather than the 2-(2-hydroxyl-1,1-diarylethoxy)-2-methylpropanenitrile radical (15). Our results are in agreement with the experimental results for the aerobic oxidative cleavage of the geminal disubstituted alkenes. Our results also demonstrate that the epoxide derivatives can be formed as an intermediate under the reaction conditions. This reaction is not applicable for pyridine derivatives due to the conversion of vinylpyridine derivatives to N-oxide derivatives.

Graphical abstract: A computational study of the reaction mechanism of 2,2-azobis(isobutyronitrile)-initiated oxidative cleavage of geminal alkenes

Supplementary files

Article information

Article type
Paper
Submitted
16 8月 2021
Accepted
08 10月 2021
First published
19 10月 2021

Org. Biomol. Chem., 2021,19, 9483-9490

A computational study of the reaction mechanism of 2,2-azobis(isobutyronitrile)-initiated oxidative cleavage of geminal alkenes

S. Eşsiz and U. Bozkaya, Org. Biomol. Chem., 2021, 19, 9483 DOI: 10.1039/D1OB01607E

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