首页> 外文期刊>Journal of new materials for electrochemical systems >Electrochemical Characterization of Bis-(10Hphenothiazin-3-yl)-methane Derivatives Obtained by Microwave Assisted Organic Synthesis
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Electrochemical Characterization of Bis-(10Hphenothiazin-3-yl)-methane Derivatives Obtained by Microwave Assisted Organic Synthesis

机译:微波辅助有机合成获得的双-(10Hphenothiazin-3-yl)-甲烷衍生物的电化学表征

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摘要

Microwave assisted heating in pressurized systems is proved to be an efficient technique for the preparation of bis(10Hphenothiazin-3-yl)-methane and bis-(10Hphenothiazin-3-yl)-phenyl-methane derivatives by the condensation of phenothiazine with aldehydes in acidic media Redox activity of bis-(10Hphenothiazin-3-yl)-methane derivatives was demonstrated by cyclic voltammetry experiments and modified electrodes were prepared by adsorption of these compounds on spectrographic graphite. The cyclic voltammograms recorded for a range of potential scan rates (10-400 mV s(-1)) showed a linear dependence of the peak currents on the electrode potential scan rate. The estimated electrochemical parameters show redox activity, stability and good adsorption properties on graphite.
机译:加压系统中的微波辅助加热被证明是通过吩噻嗪与醛缩合制备双(10Hphenothiazin-3-yl)-甲烷和双(10hphenothiazin-3-yl)-苯基-甲烷衍生物的有效技术。通过循环伏安法实验证明了双-(10Hphenothiazin-3-yl)-甲烷衍生物的氧化还原活性,并通过将这些化合物吸附在光谱石墨上制备了修饰的电极。记录的一系列电位扫描速率(10-400 mV s(-1))的循环伏安图显示,峰值电流与电极电位扫描速率呈线性关系。估计的电化学参数显示出氧化还原活性,稳定性和对石墨的良好吸附性能。

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