Preparation and properties of polythiophene with phenylacetylene substituent

被引:9
作者
Hayashi, H [1 ]
Yamamoto, T [1 ]
机构
[1] Tokyo Inst Technol, Chem Resources Lab, Midori Ku, Yokohama, Kanagawa 2268503, Japan
关键词
pi-conjugated polymer; zelovalent nickel complex; zelovalent palladium complex; phenylacetylene; polythiophene;
D O I
10.1295/koron.58.221
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Dehalogenative polycondensation of 2,5-dibromo-3-(4-alkylphenylethynyl) thiophenes with zerovalent nickel complexes afforded poly-[3-(4-alkylphenylethynyl) thiopbene-2,5-diyl]s in good yields. analytical, IR, and C-13 NMR data agreed with the suucture of the polymers. The UV-vis, absorption peak of the polymer appeared at a longer wavelength than the peaks of poly(3-alkylthiophene) and poly(3-arylthiophene). suggesting the formation of a larger effective pi -conjugation system due to negligible steric repulsion between the substituent and the neighboring thiophene unit. Cyclic voltammetry of the polymer indicated that alkylphenylethynyl substituent behaved as an electron-withdrawing unit.
引用
收藏
页码:221 / 226
页数:6
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