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首页> 外文期刊>Electroanalysis >Electrochemical oxidation of diethyl 1,4-dihydro-2,4,6-trimethyl-3,5-pyridinedicarboxylate on a glassy carbon electrode as model compound of NADH
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Electrochemical oxidation of diethyl 1,4-dihydro-2,4,6-trimethyl-3,5-pyridinedicarboxylate on a glassy carbon electrode as model compound of NADH

机译:1,4-二氢-2,4,6-三甲基-3,5-吡啶二羧酸二乙酯在NADH的模型化合物上的电化学氧化

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摘要

The electrooxodation of diethyl 1,4-dihydro-2,4,6-trimethyl-3,5-pyridinedicarboxylate (DTP) in ethanol/water solutions on a glassy carbon electrode has been studied by linear-sweep cyclic voltammetry. Convolution voltammetry was used to analyze the I-E curves. From the experimental results it was concluded that in acidic media, the rate-determining step, r.d.s., was the deprotonation of the radical cation formed after the first one-electron transfer. In basic media, the mechanism consisted of a DISP1 scheme in which r.d.s. is the uptake of an H+ ion by both the OH- ion and the basic components of the buffer. The relative rate constant of the carbonate ion with respect to the OH- is calculated. [References: 35]
机译:通过线性扫描循环伏安法研究了在乙醇/水溶液中的玻璃碳电极上的1,4-二氢-2,4,6-三甲基-3,5-吡啶二甲酸二乙酯的电氧化。卷积伏安法用于分析I-E曲线。从实验结果可以得出结论,在酸性介质中,决定速率的步骤r.d.s.是第一次单电子转移后形成的自由基阳离子的去质子化。在基本媒体中,该机制由DISP1方案组成,其中r.d.s.是OH-离子和缓冲液基本成分对H +离子的吸收。计算碳酸根离子相对于OH-的相对速率常数。 [参考:35]

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