Nitroxide-mediated homo- and block copolymerization of styrene and multifunctional acryl- and methacryl derivatives

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • MZ Yin - (Author)
  • T Krause - (Author)
  • M Messerschmidt - (Author)
  • WD Habicher - (Author)
  • B. Voit - , Leibniz Institute of Polymer Research Dresden (Author)

Abstract

The ability of different alkoxyamines (11, 12, 13, 14, and 15) to initiate controlled radical polymerization of styrene was evaluated. Among them, 2-hydroxymethyl-2- [(2-methyl-1-phenyl-propyl)-(1-phenyl-ethoxy)-amino]-propane-1,3-diol (15) gave the highest polymerization rate of styrene, and the best control over the molecular weight and the molecular weight distribution of polystyrene. Kinetic studies confirmed that with initiator 15 the polymerization of styrene proceeded in a controlled way. The controlled radical homopolymerization of multifunctional acryl- and methacryl derivatives using initiator 15 could not be realized as demonstrated by the high polydispersities (PD) obtained. However, it was possible to polymerize multifunctional acryl- and methacryl derivatives using a polystyrene macroinitiator (Pst) and, thus, novel amphiphilic block copolymers with a narrow molecular weight distribution were obtained. (c) 2005 Wiley Periodicals, Inc.

Details

Original languageEnglish
Pages (from-to)1873-1882
Number of pages10
JournalJournal of Polymer Science, Part A: Polymer Chemistry
Volume43
Issue number9
Publication statusPublished - 1 May 2005
Peer-reviewedYes
Externally publishedYes

External IDs

Scopus 19944373415
ORCID /0000-0002-4531-691X/work/148607702

Keywords

Keywords

  • Alkoxyamine, Amphiphilic block copolymers, Multifunctional acryl- and methacryl derivatives, Nitroxide-mediated radical polymerization