Volume 217, Issue 20 p. 2201
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Free Access

Macromol. Chem. Phys. 20/2016

Kyle J. Sykes

Kyle J. Sykes

Chemistry, School of Science and Technology, University of New England, Armidale, NSW, 2351 Australia

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Simon Harrisson

Simon Harrisson

Laboratoire Interactions Moléculaires et Réactivité Chimique et Photochimique, UMR 5623 CNRS-UPS Toulouse, Université Paul Sabatier Toulouse, 118 route de Narbonne, 31062 Toulouse Cedex 9, France

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Daniel J. Keddie

Daniel J. Keddie

Chemistry, School of Science and Technology, University of New England, Armidale, NSW, 2351 Australia

School of Biology, Chemistry and Forensic Science, Faculty of Science and Engineering, University of Wolverhampton, Wulfruna Street, Wolverhampton, WV1 1LY UK

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First published: 18 October 2016

Graphical Abstract

Front Cover: This work represents the RAFT copolymerization of the phosphine-functional styrenic monomer, 4-(diphenylphosphino)styrene, with styrene. Copolymerization behaviour is explored to establish the statistical distribution of the phosphine functionality within the copolymer. There is a strong tendency for the phosphine-bearing monomer to homopolymerize whilst styrene prefers to copolymerize. This results in the polymer possessing gradient-microstructure from preferential incorporation of phosphine-based functionality. Further details can be found in the article by Kyle J. Sykes, Simon Harrisson, and Daniel J. Keddie* on page 2310.

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