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Multi-stimuli responsive supramolecular diblock copolymers

  • L. Sambe
  • , K. Belal
  • , F. Stoffelbach
  • , J. Lyskawa
  • , F. Delattre
  • , M. Bria
  • , F. X. Sauvage
  • , M. Sliwa
  • , V. Humblot
  • , B. Charleux
  • , G. Cooke
  • , P. Woisel
  • Université de Lille
  • UMR 7610
  • Sorbonne Université
  • Unité de Chimie Environnementale et Interactions sur le Vivant
  • Laboratoire de Spectrochimie Infrarouge et Raman, Université des Sciences et Technologies de Lille, UMR-CNRS 8516
  • Laboratoire de Réactivité de Surface
  • IGFL, Université de Lyon, Université Lyon 1
  • Glasgow Centre for Physical Organic Chemistry
  • University of Glasgow

Research output: Contribution to journalArticlepeer-review

31 Citations (Scopus)

Abstract

A well-defined cyclobis(paraquat-p-phenylene) (CBPQT4+) end-functionalized poly(n-butyl acrylate) 3 was prepared via RAFT polymerization using a new trithiocarbonate CBPQT4+ derivative 2 as a reversible chain transfer agent. We have shown that the electron-poor CBPQT4+ moiety at the α-chain-end could be specifically modified by complex formation with various functionalized macromolecules featuring complementary electron rich end groups, thereby leading to the corresponding supramolecular diblock copolymers. The latter could be conveniently disassembled upon heating, by applying electrochemical redox processes or by the addition of a competing molecular guest. Furthermore, we can generate new diblock architectures upon the addition of an appropriately functionalized polymer. We also describe preliminarily results regarding the formation of nanostructured architectures both in solution and in thin films.

Original languageEnglish
Pages (from-to)1031-1036
Number of pages6
JournalPolymer Chemistry
Volume5
Issue number3
DOIs
Publication statusPublished - 7 Feb 2014
Externally publishedYes

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