首页> 外文期刊>Indian Journal of Chemistry, Section B. Organic Including Medicinal >Synthesis and electrochemical investigations on 1-[4'-(5',6'-dimethoxypyrimidino-sulphonamoyl)phenylamino]-3-chloro-4,4-diphenylazetidin-2-one
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Synthesis and electrochemical investigations on 1-[4'-(5',6'-dimethoxypyrimidino-sulphonamoyl)phenylamino]-3-chloro-4,4-diphenylazetidin-2-one

机译:1- [4'-(5“,6”-二甲氧基嘧啶-磺酰胺基)苯氨基] -3-氯-4,4-二苯基氮杂环丁烷-2-酮的合成及电化学研究

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摘要

The electrochemical reduction of 1-[4'-(5",6"-dimethoxypyrimidinosulphonamoyl)phenylamino]-3-chloro-4,4-diphenylazetidin-2-one has been studied over a wide pH range at dropping mercury and glassy carbon electrodes. It gives diffusion-controlled, irreversible and single two-electron wave corresponding to the reduction of -NH-N- moiety. On the basis of polarography, linear sweep and cyclic voltammetry, coulometry, IR and ~1H NMR spectral studies, and product identification, a reaction mechanism is suggested to account for the reduction of these compounds. Kinetic parameters, i.e., charge-transfer coefficient (#alpha#n) and forward rate constant (K~0_(f,h)) have also been calculated.
机译:在宽的pH范围内,在滴落汞和玻璃碳电极的情况下,已研究了1- [4'-(5“,6”-二甲氧基嘧啶基磺酰胺基)苯基氨基] -3-氯-4,4-二苯基氮杂环丁烷-2-one的电化学还原。它给出了与-NH-N-部分还原相对应的扩散控制的,不可逆的单电子波。根据极谱法,线性扫描和循环伏安法,库仑法,IR和〜1H NMR光谱研究以及产物鉴定,建议采用反应机理解释这些化合物的还原。还计算了动力学参数,即电荷转移系数(#alpha#n)和正向速率常数(K〜0_(f,h))。

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