Multi-stimuli responsive supramolecular diblock copolymers

Literature Information

Publication Date 2013-10-03
DOI 10.1039/C3PY01093G
Impact Factor 5.582
Authors

L. Sambe, F. Stoffelbach, J. Lyskawa, F. Delattre, M. Bria, F. X. Sauvage, M. Sliwa, V. Humblot, B. Charleux, G. Cooke, P. Woisel


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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.

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Polymer Chemistry

Polymer Chemistry
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Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.

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