Volume 28, Issue 12 pp. 3271-3278
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The reactivities of diarylbutadienes towards the benzoyloxy radical: the cases of 1-(1′-naphthyl)-4-phenylbuta-l,3-diene and 1,4-Di (1′-Naphthyl)buta-1,3-Diene

J. C. Bevington

Corresponding Author

J. C. Bevington

Department of Chemistry, The University, Lancaster LA1 4YA, United Kingdom

Department of Chemistry, The University, Lancaster LA1 4YA, United KingdomSearch for more papers by this author
S. W. Breuer

S. W. Breuer

Department of Chemistry, The University, Lancaster LA1 4YA, United Kingdom

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T. N. Huckerby

T. N. Huckerby

Department of Chemistry, The University, Lancaster LA1 4YA, United Kingdom

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Rosie F. D. Jones

Rosie F. D. Jones

Department of Chemistry, The University, Lancaster LA1 4YA, United Kingdom

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C. A. Barson

C. A. Barson

School of Chemistry, The University, Birmingham B15 2TT, United Kingdom

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First published: November 1990
Citations: 7

Abstract

A study has been made of end-groups in poly(methyl methacrylate) prepared using benzoyl peroxide as initiator and either 1-(1′-naphthyl)4-phenylbuta-1,3-diene or 1,4-di(1′-naphthyl)buta-1,3-diene as additive. At 60°C, these dienes are 500–600 times as effective as methyl methacrylate in capturing benzoyloxy radicals and more than twice as effective as 1,4-diphenylbuta-1,3-diene.

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