Synthesis and optical properties of 1,1-binaphthyl-thiophene alternating copolymers with main chain chirality

被引:22
|
作者
Kawabata, Kohsuke [1 ]
Goto, Hiromasa [1 ]
机构
[1] Univ Tsukuba, Fac Pure & Appl Sci, Div Mat Sci, Tsukuba, Ibaraki 3058573, Japan
基金
日本学术振兴会;
关键词
FLUORENE COPOLYMERS; CONJUGATED POLYMERS; CONFORMATION; AGGREGATION; RECOGNITION; DERIVATIVES; INDUCTION;
D O I
10.1039/c2jm35594a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A series of axially chiral 1,1-binaphthyl-thiophene copolymers were synthesized by Migita-Kosugi-Stille polycondensation and electrochemical polymerization. The polymers exhibit circular dichroism not only in the ultraviolet region but also in the visible region, both in solution and film states. Optical and electrochemical properties of the polymers are in good agreement with theoretical results obtained by density functional theory calculations. Although effective conjugation of the polymers was cleaved at the orthogonally oriented two naphthalene rings in the 1,1-binaphthyl unit, the electrochemically synthesized polymer film shows good electrochemical redox behavior with repeatable changes in optical absorption and circular dichroism. The changes in circular dichroism may reflect a change in the dihedral angle of the binaphthyl unit caused by reorientation of conjugated main chains between oxidized and neutral states.
引用
收藏
页码:23514 / 23524
页数:11
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