Hydrogen bond complexation of dimethyl-[1-butyl-2,4-dioxo(1H,3H)pyrimido]tetrathiafulvalene with aminopyridine derivatives probed by cyclic voltammetry

被引:22
作者
Goldenberg, LM [1 ]
Neilands, O
机构
[1] Russian Acad Sci, Inst Chem Phys Res, Chernogolovka 142432, Russia
[2] Riga Tech Univ, Dept Organ Chem, LV-1048 Riga, Latvia
基金
俄罗斯基础研究基金会;
关键词
voltammetric response; hydrogen bond; tetrathiafulvalene; molecular recognition;
D O I
10.1016/S0022-0728(98)00456-2
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The cyclic voltammetric response of dimethyl-[1-butyl-2,4-dioxo(1H,3H)pyrimido]tetrathiafulvalene 1 is studied in the presence of aminopyridine derivatives. The first oxidation potential of 1 increases with an increase in 2,6-di(N-acetylamino)pyridine concentration. with the maximum shift being 30 mV. This is assigned to the formation of a multihydrogen-bond complex in the neutral state with the binding constant estimated to be ca. 1000 M-1. An irreversible following chemical reaction is suggested for the explanation of the complicated behaviour of the second redox wave of 1 in the presence of 2,6-di(N-acetylamino)pyridine. (C) 1999 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:212 / 217
页数:6
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