Synthesis and redox behavior of benzo-1,3-dithiafulvalenes incorporating ferrocene moiety as redox active ligands

被引:7
|
作者
Sarhan, AE [1 ]
Izumi, T [1 ]
机构
[1] Yamagata Univ, Fac Engn, Dept Chem & Chem Engn, Yonezawa, Yamagata 9928510, Japan
关键词
Fc-DTF; synthesis; organic conducting materials; electrochemical properties;
D O I
10.1016/S0379-6779(03)00383-7
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A simple route for the synthesis of several new benzo-1,3-dithiafulvalenes incorporated with ferrocene (Fc) moiety is reported. The benzo-1,3-dithiafulvalenes (6a-f) were synthesized by introducing a ferrocene coordination function as new donor compounds based on the Wittig-Horner olefenation method. The redox behavior of the new donor compounds was investigated in comparison with the ferrocene and established 1,4-dithiafulvalenes by cyclic voltammetry. Two couples of redox peaks were observed for both ferrocene and extended dithiafulvalene (DTF). (C) 2003 Elsevier B.V. All rights reserved.
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页码:95 / 100
页数:6
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