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The thermal decomposition of 2,2 '-azobis(2-methylpropionitrile) in the presence of 2,6-Di-t-butyl and 2,6-diphenyl-1,4-benzoquinone

Hageman, Hendrik J. (2000) The thermal decomposition of 2,2 '-azobis(2-methylpropionitrile) in the presence of 2,6-Di-t-butyl and 2,6-diphenyl-1,4-benzoquinone. European Polymer Journal, 36 (2). pp. 345-350. ISSN 0014-3057. (doi:10.1016/S0014-3057(99)00074-9) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:16176)

The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided.
Official URL:
http://dx.doi.org/10.1016/S0014-3057(99)00074-9

Abstract

The thermal decem position of 2,2'-azobis(2-methylpropionitrile) in the presence of 216-di-t-butyl-1,4-benzoquinone results in the formation of 2,6-di-t-butyl-1,4-di(2-cyano-2-propoxy)benzene as the only addition product, whereas the thermal decomposition of the azo compound in the presence of 2,6-diphenyl-1,4,benzoquinone gives rise to the formation of the corresponding diether (major product), together with smaller amounts of both possible monoethers. 2,5-Di-t-butyl-1,4-benzoquinone failed to give any addition products, in agreement with earlier reports. Possible mechanisms are discussed.

Item Type: Article
DOI/Identification number: 10.1016/S0014-3057(99)00074-9
Uncontrolled keywords: 2,6-di-t-butyl-1,4-benzoquinone; 2,6-diphenyl-1,4-benzoquinone; addition of 2-cyano-2-propyl radicals
Subjects: Q Science > QD Chemistry
Divisions: Divisions > Division of Natural Sciences > Biosciences
Divisions > Division for the Study of Law, Society and Social Justice > School of Social Policy, Sociology and Social Research
Depositing User: O.O. Odanye
Date Deposited: 01 May 2009 00:58 UTC
Last Modified: 16 Nov 2021 09:54 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/16176 (The current URI for this page, for reference purposes)

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