Issue 42, 2015

Controlling the synthesis of degradable vinyl polymers by xanthate-mediated polymerization

Abstract

The copolymerization of vinyl acetate (VAc) and 2-methylene-1,3-dioxepane (MDO), as well as the homopolymerization of MDO in the presence of a p-methoxyphenyl xanthate chain transfer agent (CTA) is reported and comparison of the homopolymerization of MDO with other known xanthates was also investigated. In depth investigation showed loss of the xanthate functionality was a result of Z-group fragmentation leading to the formation of carbonodithioate groups, as confirmed by 13C NMR spectroscopy. The use of the xanthate with a substituted phenyl Z-group drastically reduces fragmentation through the Z-group and hence significantly increases chain-end retention during the polymerization using the RAFT/MADIX technique. Post-polymerization modification of the chain-end of poly(MDO) was achieved by in situ aminolysis and base-catalyzed Michael addition of propargyl methacrylate onto the terminal thiol to form alkyne functional poly(MDO).

Graphical abstract: Controlling the synthesis of degradable vinyl polymers by xanthate-mediated polymerization

Supplementary files

Article information

Article type
Paper
Submitted
23 Jul 2015
Accepted
29 Aug 2015
First published
02 Sep 2015
This article is Open Access
Creative Commons BY license

Polym. Chem., 2015,6, 7447-7454

Author version available

Controlling the synthesis of degradable vinyl polymers by xanthate-mediated polymerization

C. A. Bell, G. G. Hedir, R. K. O'Reilly and A. P. Dove, Polym. Chem., 2015, 6, 7447 DOI: 10.1039/C5PY01156F

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