Development of a Universal Chain-Growth Polymerization Protocol of Conjugated Polymers: Toward a Variety of All-Conjugated Block-Copolymers

被引:56
|
作者
Verswyvel, Michiel [1 ]
Verstappen, Pieter [1 ]
De Cremer, Lieven [1 ]
Verbiest, Thierry [1 ]
Koeckelberghs, Guy [1 ]
机构
[1] Katholieke Univ Leuven, Dept Chem, Lab Mol Elect & Photon, B-3001 Louvain, Belgium
关键词
all-conjugated block-copolymers; block-copolymers; conjugated polymers; living polymerizations; poly(thiophene); poly(fluorene); TRANSFER CONDENSATION POLYMERIZATION; CATALYST-TRANSFER POLYCONDENSATION; PREFERENTIAL OXIDATIVE ADDITION; WELL-DEFINED POLYTHIOPHENE; GRIGNARD METATHESIS METHOD; CROSS-COUPLING REACTIONS; SUPRAMOLECULAR CHIRALITY; PRECISION SYNTHESIS; MAGNESIUM EXCHANGE; MOLECULAR-WEIGHT;
D O I
10.1002/pola.25014
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
This manuscript reports a universal chain-growth polymerization protocol for conjugated polymers. Herein, the Pd-based catalyst moiety dissociates from the growing active center into the solution and therefore, the controlled chain-growth character is not relying on any specific, system-related complexation, as is the case in polymerization methods reported before. This makes the protocol applicable on a broad range of monomers and, furthermore, also allows an easy one-pot synthesis of block-copolymers by successive monomer addition. A chain-growth polymerization mechanism for poly(3-hexylthiophene) (P3HT) and poly(9,9-dioctylfluorene) (PF) and all-conjugated block-copolymers of them is presented. Moreover, the sequence of monomer addition in the synthesis of these conjugated block-copolymers is unimportant, which is unique. (C) 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 49: 5339-5349, 2011
引用
收藏
页码:5339 / 5349
页数:11
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