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Electrochemical Reduction Behaviour of α-Methylbenzylchloride

机译:α-甲基苄基氯的电化学还原行为

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摘要

Cyclic voltammetry at hanging mercury drop electrode (HMDE) and differential pulse polarography at dropping mercury electrode (DME) arc used to two-electron cleavage of carbon-halogen bond in α-methylbenzylchloride in the presence of tetramelhylammonium hexafluorophosphate (TMAHP), tetraethylammonium bromide (TEAB), tetra-n-propylammonium perchlorate (TPAP), and tetrabutylammonium iodide (TBAI) as the supporting electrolytes. The reduction potentials of α-methylbenzylchloride are found to be in the range―2.14 to―2.56V vs Ag/AgCl and are shown to be sensitive to the nature of the cation of the supporting electrolyte. As the size of the telraalkylammonium cation of the supporting electrolyte increases the voltammetric/polarographic peak moves towards more negative potentials. The analytical procedure is developed by differential pulse polarography for the determination of α-methylbenzylchloridc during the electrosynthesis of 2-arylpropionic acids.
机译:悬挂汞滴电极(HMDE)上的循环伏安法和液滴汞电极(DME)上的差分脉冲极谱法用于在六氟磷酸四氢铵(TMAHP),四乙基溴化铵(TMAHP)存在下对α-甲基苄基氯中的碳-卤素键进行两电子裂解TEAB),高氯酸四正丙铵(TPAP)和碘化四丁铵(TBAI)作为支持电解质。发现α-甲基苄基氯化物的还原电位相对于Ag / AgCl在〜2.14至〜2.56V范围内,并且显示出对支持电解质的阳离子的性质敏感。随着支持电解质的四烷基铵阳离子尺寸的增加,伏安/极谱峰移向更多的负电势。通过差分脉冲极谱法开发了分析方法,用于在2-芳基丙酸的电合成过程中测定α-甲基苄基氯。

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