Skip to content Skip to navigation
University of Warwick
  • Study
  • |
  • Research
  • |
  • Business
  • |
  • Alumni
  • |
  • News
  • |
  • About

University of Warwick
Publications service & WRAP

Highlight your research

  • WRAP
    • Home
    • Search WRAP
    • Browse by Warwick Author
    • Browse WRAP by Year
    • Browse WRAP by Subject
    • Browse WRAP by Department
    • Browse WRAP by Funder
    • Browse Theses by Department
  • Publications Service
    • Home
    • Search Publications Service
    • Browse by Warwick Author
    • Browse Publications service by Year
    • Browse Publications service by Subject
    • Browse Publications service by Department
    • Browse Publications service by Funder
  • Help & Advice
University of Warwick

The Library

  • Login
  • Admin

Synthesis and reactivity of α,ω-homotelechelic polymers by Cu(0)-mediated living radical polymerization

Tools
- Tools
+ Tools

Simula, Alexandre, Nurumbetov, Gabit, Anastasaki, Athina, Wilson, Paul and Haddleton, David M. (2015) Synthesis and reactivity of α,ω-homotelechelic polymers by Cu(0)-mediated living radical polymerization. European Polymer Journal, 62 . pp. 294-303. doi:10.1016/j.eurpolymj.2014.07.014 ISSN 0014-3057.

Research output not available from this repository.

Request-a-Copy directly from author or use local Library Get it For Me service.

Official URL: http://dx.doi.org/10.1016/j.eurpolymj.2014.07.014

Request Changes to record.

Abstract

Telechelic poly(n-butyl acrylate) and poly[poly(ethylene glycol) methyl ether acrylate] are obtained with high monomer conversions and narrow molecular weight distributions (Ð < 1.2) by Cu(0)-mediated living radical polymerization (SET-LRP). The high end group fidelity of the polymer is confirmed by a combination of 1H NMR and MALDI-ToF-MS analysis. The reactivity of the telechelics is exploited to yield amphiphilic BAB triblocks, by sequential addition of a second monomer, which self-assemble in water. Furthermore, nucleophilic thiol-bromine substitution using 2-mercaptoethanol post-polymerization enables the incorporation of primary alcohols on both the α- and ω-polymer chain ends. The presence and reactivity of hydroxyl end-groups is confirmed upon reaction with isocyanates and further exploited to induce the ring opening polymerization (ROP) of ε-caprolactone.

Item Type: Journal Article
Divisions: Faculty of Science, Engineering and Medicine > Science > Chemistry
Journal or Publication Title: European Polymer Journal
Publisher: Pergamon
ISSN: 0014-3057
Official Date: January 2015
Dates:
DateEvent
January 2015Published
1 August 2014Available
10 July 2014Accepted
Volume: 62
Page Range: pp. 294-303
DOI: 10.1016/j.eurpolymj.2014.07.014
Status: Peer Reviewed
Publication Status: Published
Access rights to Published version: Restricted or Subscription Access

Request changes or add full text files to a record

Repository staff actions (login required)

View Item View Item
twitter

Email us: wrap@warwick.ac.uk
Contact Details
About Us