首页> 外文期刊>Journal of Applied Polymer Science >Electropolymerization and properties of 3,4-ethylenedioxythiophene backbone polymer with tetrathiafulvalene as pendant
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Electropolymerization and properties of 3,4-ethylenedioxythiophene backbone polymer with tetrathiafulvalene as pendant

机译:以四硫富瓦烯为侧基的3,4-乙撑二氧噻吩骨架聚合物的电聚合及性能

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摘要

Three 3,4-ethylenedioxythiophene (EDOT) derivatives, including an EDOT-tetrathiafulvalene (TTF) derivative, were synthesized by Steglich esterification of carboxylic acids with hydroxymethyl EDOT (3,4- ethylenedioxythiophene methanol). The UV spectra showed that there was no distinctive intramolecular interaction for the EDOT-TTF monomer between the EDOT and the TTF moieties in the ground state; however, the cyclic voltammetry responses implied that such intramolecular interaction occurred. Electropolymerization in excessive potential could bring in strong overoxidation effects and degradation in the polymer film. The polymers were simulated using density functional theory with Gaussian03 package and the optimized HOMO and LUMO state were figured out. The conductivity of TTF-polymer was 6 S·cm~(-1) obtained by galvano station and 4.8 × 10~(-3) S·cm~(-1) obtained by potentiostatic electropolymerization after doping with 7,7,8,8-tetracyanoquinodimethane. The results indicated that this polymer was a reasonable candidate for conducting materials and it was meaningful to increase the conductive dimensions of TTF polymers by chemical doping.
机译:通过将羧酸与羟甲基EDOT(3,4-乙撑二氧噻吩甲醇)进行Steglich酯化反应,合成了3种3,4-乙撑二氧噻吩(EDOT)衍生物,包括EDOT-四硫富瓦烯(TTF)衍生物。紫外光谱表明,在基态下,EDOT和TTF部分之间没有明显的EDOT-TTF单体分子内相互作用。然而,循环伏安法的响应暗示发生了这种分子内相互作用。过高电势下的电聚合会带来强烈的过氧化作用,并导致聚合物膜降解。使用密度泛函理论和高斯03软件包对聚合物进行了模拟,得出了最佳的HOMO和LUMO状态。掺杂7、7、8后,通过电电流法测得的TTF聚合物的电导率为6 S·cm〜(-1),通过恒电位电聚合得到的电导率为4.8×10〜(-3)S·cm〜(-1), 8-四氰基喹二甲烷。结果表明该聚合物是用于导电材料的合理候选物,并且通过化学掺杂来增加TTF聚合物的导电尺寸是有意义的。

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