首页> 外文期刊>Proceedings of the Indian Academy of Sciences. Chemical Sciences >Kinetics and mechanism of the oxidation of phosphinic, phenylphosphinic and phosphorous acids by benzyltrimethylammonium dichloroiodate
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Kinetics and mechanism of the oxidation of phosphinic, phenylphosphinic and phosphorous acids by benzyltrimethylammonium dichloroiodate

机译:二氯碘甲烷苄基三甲基铵氧化次膦酸,苯次膦酸和亚磷酸的动力学和机理

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摘要

Oxidation of lower phosphorus oxyacids by benzyltrimethylammonium dichloroiodate (BTACI), in the presence of zinc chloride, resulted in the formation of the corresponding oxyacids with phosphorus in a higher oxidation state. The reaction is first order with respect to the concentration of BTACI, oxyacid and zinc chloride. The reaction exhibited the presence of a substantial kinetic isotope effect. Addition of benzyltrimethylammonium chloride enhances the reaction rate. It is proposed that the reactive oxidizing species is [PhCH_2Me_3N]~ + [Zn_2Cl_6]~-(2) I~+. It has been shown that the pentacoordinated tautomer of the phosphorus oxyacid is the reactive reductant. A mechanism involving a hydride-ion transfer from the P-H bond to the oxidant in the rate-determining step has been postulated.
机译:在氯化锌存在下,苄基三甲基二氯碘酸铵(BTACI)氧化低磷含氧酸导致相应的含氧酸与磷形成较高的氧化态。关于BTACI,含氧酸和氯化锌的浓度,反应是一级的。该反应显示出基本的动力学同位素效应。加入苄基三甲基氯化铵可提高反应速率。提出反应性氧化物质为[PhCH_2Me_3N]〜+ [Zn_2Cl_6]〜-(2)I〜+。已经表明,含氧磷酸的五配位互变异构体是反应性还原剂。已经提出了在速率确定步骤中涉及从P-H键到氧化剂的氢离子转移的机理。

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