Imidazolidinone nitroxide-mediated polymerization

Y. K. Chong, Frances Ercole, Graeme Moad, Ezio Rizzardo, San H. Thang, Albert G. Anderson

Research output: Contribution to journalArticleResearchpeer-review

83 Citations (Scopus)

Abstract

Derivatives of 2,2,5,5-tetraalkylimidazolidin-4-one-l-oxyl have been found to offer significant advantages over many of the nitroxides previously employed in nitroxide-mediated polymerization: homopolymers [e.g., polystyrene and poly(alkyl acrylate)], statistical copolymers [e.g., poly(styrene-coacrylonitrile)], and block copolymers [e.g., poly(4-methylstyrene)-&Zoc&-polystyrene and poly(n-butyl acrylate)-6/oc&-polystyrene] can be synthesized with controlled molecular weight, narrow molecular weight distribution, and defined end group functionality. The effect of substituants a to the nitroxide nitrogen and at the transannular nitrogen on the outcome of polymerization is explored. Appropriate selection of these substituents provides polymers of lower polydispersities than, for example, 2,2,6,6-tetramethyIpiperidin-2-oxyl and derivatives. The nitroxides are synthesized from readily available precursors by a simple experimental route. Moreover, they are subject to fewer side reactions. In particular, disproportionation between the propagating radical with nitroxide appears to be of lesser significance.

Original languageEnglish
Pages (from-to)6902-6903
Number of pages2
JournalMacromolecules
Volume32
Issue number21
Publication statusPublished - 19 Oct 1999

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