Stimuli-responsive brush-shaped conjugated polymers with pendant well-defined poly(vinyl ether)s

被引:18
|
作者
Motoyanagi, Jin [1 ]
Ishikawa, Taketo [1 ]
Minoda, Masahiko [1 ]
机构
[1] Kyoto Inst Technol, Grad Sch Sci & Technol, Fac Mol Chem & Engn, Sakyo Ku, Kyoto 6068585, Japan
基金
日本学术振兴会;
关键词
brush-shaped polymers; living polymerization; macromonomers; poly(vinyl ethers); stimuli-sensitive polymers; SIGNAL AMPLIFICATION; MOLECULAR DESIGN; CHEMICAL SENSORS; SOLAR-CELLS; SOLID-STATE; POLYELECTROLYTES; AGGREGATION; COPOLYMERS; BEHAVIOR; MODEL;
D O I
10.1002/pola.28220
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
For the synthesis of brush-shaped conjugated polymers consisting of a poly(phenylene butadiynylene) backbone and well-defined poly(vinyl ether) (polyVE) side chains, we designed polyVE-based macromonomers bearing a diethynyl benzene group at the terminus and applied them to the grafting through synthesis. The macromonomer (DE-PIBVE) was synthesized by living cationic polymerization of isobutyl VE (IBVE) using a functionalized initiator (TMS-DEVE-TFA) having a TMS protected diethynyl benzene moiety, followed by deprotection of the TMS groups. As a result, we succeeded in the synthesis of the target brush-shaped conjugated polymers [poly(DE-PIBVE)] by oxidative coupling reaction of the diethynyl benzene groups. We found that the solution of poly(DE-PIBVE) with a specific side chain length exhibited solvatochromism and thermochromism depending on the polarity of the media employed. This phenomenon was attributed to self-assembly in polar media due to the intermolecular - interaction between neighboring conjugated polymer backbones, where the self-assembly behavior would be closely related to the pendant polyVE structure. (c) 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016, 54, 3318-3325
引用
收藏
页码:3318 / 3325
页数:8
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