EFFECT OF SELF-PROTONATION ON THE POLAROGRAPHIC BEHAVIOR OF SOME DERIVATIVES OF 2,1,3-THIADIAZOLE IN AQUEOUS AND DIMETHYLFORMAMIDE SOLUTIONS.

被引:0
|
作者
Tsveniashvili, V.Sh.
Gaprindashvili, V.N.
Tskalobadze, L.A.
机构
来源
Soviet Electrochemistry (English Translation of Elektro-Khimiia) | 1975年 / 11卷 / 04期
关键词
ELECTROCHEMISTRY;
D O I
暂无
中图分类号
学科分类号
摘要
The effect of several proton-donating substituents upon the polarographic behavior of 2,1,3-thiadiazole has been studied. It is shown that, as a result of self-protonation, separate reduction of monoprotonated and unprotonated molecules of the depolarizer takes place in aqueous neutral, nonbuffered media. It has been found that the chief factor determining the half-wave potential shift towards more positive values in dimethylformamide solutions is the proton-donating effect of the carboxy or hydroxy groups in the depolarizer.
引用
收藏
页码:485 / 488
相关论文
共 38 条