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Anthradithiophene Derivatives Substituted at the 2,8-Positions by Formyl and Triphenylamine Units: Synthesis, Optical, and Electrochemical Properties

机译:甲硫基和三苯胺单元在2,8-位取代的蒽硫代衍生物:合成,光学和电化学性质

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摘要

The synthesis and characterization of two new anthradithiophene (ADT) derivatives substituted by thiophenyl or 2-octylthiophenyl units at the 5,11-positions and donor (triphenylamine) or acceptor (aldehyde functions) moieties at the 2,8-positions of their backbone are described. Optical measurements were performed to evaluate the effect of electron-rich/-poor substituents on their stability towards photo-oxidation and were supported by quantum chemical calculations and cyclic voltammetry experiments. Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
机译:两种新的邻位噻吩(ADT)衍生物的合成和表征分别是在其5,11位上的噻吩基或2-辛基噻吩基和在其骨架的2,8位上的施主(三苯胺)或受体(醛官能)部分描述。进行光学测量以评估富电子/贫电子取代基对其光氧化稳定性的影响,并得到量子化学计算和循环伏安法实验的支持。版权所有©2011 WILEY-VCH Verlag GmbH&Co. KGaA,Weinheim。

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