详细信息

两个多核四硫代富瓦烯类衍生物的合成和电化学行为  ( EI收录)  

Synthesis of Two Polynuclear Tetrathiafulvalene Derivatives and Their Behaviour of Cyclic Voltammetry

文献类型:期刊文献

中文题名:两个多核四硫代富瓦烯类衍生物的合成和电化学行为

英文题名:Synthesis of Two Polynuclear Tetrathiafulvalene Derivatives and Their Behaviour of Cyclic Voltammetry

作者:沈永嘉[1];董长征[1];倪彩英[1]

机构:[1]华东理工大学精细化工研究所

年份:1995

卷号:16

期号:7

起止页码:1059

中文期刊名:高等学校化学学报

外文期刊名:Chemical Journal of Chinese Universities

收录:CSTPCD;;EI(收录号:1995112926277);Scopus;北大核心:【北大核心1992】;CSCD:【CSCD2011_2012】;

基金:国家教育委员会留学回国人员基金

语种:中文

中文关键词:四硫代富瓦烯;合成;电子给体;循环伏安;氧化电位

外文关键词:Tetrathiafulvalene, Synthesis, Donor, Cyclic voltammetry, Oxidation potential

摘要:合成了2个含3个四硫代富瓦烯单元的化合物,给出了它们的核磁共振氢谱、质谱、紫外吸收光谱及元素分析数据。用循环伏安法测定了它们的氧化还原电位,并将其与仅含1个或2个四硫代富瓦烯单元的化合物的氧化还原电位比较。发现随着分子内共轭程度的增加,分子内的库仑斥力也随之降低。
Two polynuclear tetrathiafulvalene (TTF) derivatives, which contained three TTF sub-units, were synthesized. Their 1H NMR,13C NMR, MS, and UV absorption spectra as well as cyclic voltammograms (CV) were given. The CV behaviour of the compounds was compared with that of corresponding TTF derivatives containing one or two TTF sub-units. It indicated that the coulombic repulsion in the former was lower than that in the latter, because a conjugation degree in the former was longer than in the latter.

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