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Electrooxidation of Chlorpromazine in Aqueous and Micellar Media and Spectroscopic Studies of the Derived Cationic Free Radical and Dication Species

机译:氯丙嗪在水和胶束介质中的电氧化及衍生的阳离子自由基和阳离子物种的光谱研究

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The electrochemical behaviour of chlorpromazine has been examined in phosphate buffers in aqueous as well as micellar media at a pyrolytic graphite electrode surface. 1o oxidation peaks were obtained in linear sweep voltammetry of chlorpromazine. The first peak corresponds to the formation of the cationic free radical, which on further le--oxidation gives a dication. The spectroscopic changes and kinetics of the cationic free radical and dication species generated during electrooxidation of chlorpromazine were investigated in both media. The decay of the dication was studied chronoamperometrically and was found to follow first-order kinetics with a half-life of approx -'25 ms. Surfactants affect both Ep and ip values. The anionic surfactant SDS has been found to catalyze the reaction of the free radical cation and the dication.
机译:已经在热解石墨电极表面的水性和胶束介质的磷酸盐缓冲液中检查了氯丙嗪的电化学行为。在氯丙嗪的线性扫描伏安法中获得1 vo氧化峰。第一个峰对应于阳离子自由基的形成,其在进一步的le-氧化作用下产生指示。在两种介质中研究了氯丙嗪电氧化过程中产生的阳离子自由基和阳离子物种的光谱变化和动力学。计时电流法研究了该药的衰变,发现该药遵循一阶动力学,半衰期约为-25 ms。表面活性剂会影响Ep和ip值。已经发现阴离子表面活性剂SDS可催化自由基阳离子和阳离子的反应。

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