Multi-stimuli responsive supramolecular diblock copolymers

被引:29
|
作者
Sambe, L. [1 ]
Belal, K. [1 ,2 ]
Stoffelbach, F. [2 ]
Lyskawa, J. [1 ]
Delattre, F. [3 ]
Bria, M. [1 ]
Sauvage, F. X. [4 ]
Sliwa, M. [4 ]
Humblot, V. [5 ]
Charleux, B. [6 ]
Cooke, G. [7 ]
Woisel, P. [1 ]
机构
[1] Univ Lille Nord France, UMET UMR8207, ENSCL, F-59655 Villeneuve Dascq, France
[2] UPMC Univ Paris 6 CNRS, Lab Chim Polymeres, UMR 7610, F-94200 Ivry, France
[3] Univ Littoral Cote dOpale, EA 4492, UCEIV, F-59140 Dunkerque, France
[4] Univ Lille Nord France, LASIR UMR8516, ENSCL, F-59655 Villeneuve Dascq, France
[5] UPMC Univ Paris 6 CNRS, Lab Reactivite Surface, UMR 7197, F-94200 Ivry, France
[6] Univ Lyon 1, CNRS, Lab Chim Catalyse Polymeres & Proc C2P2, CPE Lyon,UMR 5265,Equipe LCPP, F-69616 Villeurbanne, France
[7] Univ Glasgow, Sch Chem, Glasgow Ctr Phys Organ Chem, WestCHEM, Glasgow G12 8QQ, Lanark, Scotland
关键词
PSEUDO-BLOCK-COPOLYMERS; TETRATHIAFULVALENE DERIVATIVES; CYCLOBIS(PARAQUAT-P-PHENYLENE); POLYMERS; WATER; COMPLEXATION; CYCLOBIS(PARAQUAT-PARA-PHENYLENE); RELEASE; BINDING; PHENYL;
D O I
10.1039/c3py01093g
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A well-defined cyclobis(paraquat-p-phenylene) (CBPQT(4+)) end-functionalized poly(n-butyl acrylate) 3 was prepared via RAFT polymerization using a new trithiocarbonate CBPQT(4+) derivative 2 as a reversible chain transfer agent. We have shown that the electron-poor CBPQT(4+) moiety at the alpha-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.
引用
收藏
页码:1031 / 1036
页数:6
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