Monomer reactivity vs regioregularity in polythiophene derivatives: A joint synthetic and theoretical investigation.

被引:15
|
作者
Frechette, M [1 ]
Belletete, M [1 ]
Bergeron, JY [1 ]
Durocher, G [1 ]
Leclerc, M [1 ]
机构
[1] UNIV MONTREAL,DEPT CHIM,MONTREAL,PQ H3C 3J7,CANADA
关键词
polythiophene derivatives; INDO calculation; monomer reactivity; regiochemical structure;
D O I
10.1016/S0379-6779(97)80723-0
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Over the past decade, conducting polymers have gained a large interest. From the factors influencing their conductivity, the regioregularity of the chains is one of the greatest importance. A joint experimental and theoretical study on various alkyl-, alkylthio- and alkoxy-substituted thiophenes and bithiophenes shows that the reactivity of the monomer, i.e. the distribution of the unpaired electron pi-spin density on the different positions of the oxidized monomer, has a significant influence on the regioregularity of the resulting polymers. From all these results, it is clear that INDO calculations can be useful as a pre-synthetic tool for the rational design by oxidative polymerization (chemically or electrochemically) of novel regioregular and non-regioregular aromatic polymers.
引用
收藏
页码:223 / 224
页数:2
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