...
首页> 外文期刊>Journal of Chemistry >Kinetics and Mechanistic Study of the Ruthenium(III) Catalysed Oxidative Decarboxylation of L-Proline by Alkaline Heptavalent Manganese (Stopped flow technique)
【24h】

Kinetics and Mechanistic Study of the Ruthenium(III) Catalysed Oxidative Decarboxylation of L-Proline by Alkaline Heptavalent Manganese (Stopped flow technique)

机译:碱性术术术锰(STOPPRED技术)钌(III)钌(III)催化氧化脱羧的动力学和机械研究

获取原文

摘要

The kinetics of ruthenium(III) catalysed oxidation of L-Proline by permanganate in alkaline medium at a constant ionic strength has been studied spectrophotometrically using a rapid kinetic accessory. The reaction between permanganate and L-Proline in alkaline medium exhibits 2:1 stoichiometry (KMnO4: L-Proline). The reaction shows first order dependence on [permanganate] and [ruthenium(III)] and apparent less than unit order dependence each in L-Proline and alkali concentrations. Reaction rate increases with increase in ionic strength and decrease in solvent polarity of the medium. Initial addition of reaction products did not affect the rate significantly. A mechanism involving the formation of a complex between catalyst and substrate has been proposed. The activation parameters were computed with respect to the slow step of the mechanism and discussed
机译:通过快速动力学配偶分光光度法研究了在恒定离子强度下在碱性培养基中通过碱性培养基催化L-脯氨酸的催化氧化的动力学。碱性培养基中高锰酸盐和L-脯氨酸之间的反应表现出2:1化学计量(KMnO 4:L-脯氨酸)。该反应显示了对ε和[钌(III)]的第一顺序依赖性,并且在L-脯氨酸和碱浓度下,表达小于单位顺序。反应速率随着离子强度的增加而增加,并降低介质的溶剂极性。初步添加反应产物并未显着影响速率。提出了一种涉及形成催化剂和基材之间复合物的机制。相对于机制的慢速步骤计算激活参数并讨论

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号