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首页> 外文期刊>Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry >RUTHENIUM(III) CATALYZED OXIDATION OF ALIPHATIC PRIMARY AMINES BY BROMAMINE-T IN HYDROCHLORIC ACID MEDIUM - A KINETIC STUDY
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RUTHENIUM(III) CATALYZED OXIDATION OF ALIPHATIC PRIMARY AMINES BY BROMAMINE-T IN HYDROCHLORIC ACID MEDIUM - A KINETIC STUDY

机译:溴酸T在盐酸介质中钌(III)催化脂肪族初级胺的动力学研究。

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摘要

The kinetics of the ruthenium(III) catalyzed oxidation of the aliphatic primary amines n-propylamine, n-butylamine and isoamylamine, by sodium N-bromo-p-toluenesulfonamide or bromamine-T (BAT) in HCI medium has been studied in the temperature range 298-313 K. The reaction rate shows a first-order dependence each on BAT, amine, and ruthenium(III). The reaction also shows an inverse fractional-and inverse first-order dependence on acid at low and high [HCl] ranges, respectively. Added halide ions and p-toluenesulfonamide (reduction product of BAT), and variation of ionic strength of the solvent medium have no effect on the rate. The activation parameters have been evaluated. Mechanisms consistent with the kinetic data have been proposed. The protonation constant of monobromamine-T has been evaluated to be 29 +/- 2. A Taft LFE relationship is observed for the ruthenium(lll) catalyzed reaction with p* = -4.6 indicating that the electron donating groups enhance the reaction rate. An isokinetic relationship is observed with B = 355 K indicating that enthalpy factors control the rate. [References: 31]
机译:N-溴对甲苯磺酰胺钠或溴胺T(BAT)在温度下研究了钌(III)催化脂肪族伯胺正丙胺,正丁胺和异戊胺氧化的动力学反应速率在298-313 K之间。反应速率对BAT,胺和钌(III)均显示出一级依赖性。该反应还分别在低[HCl]和高[HCl]范围内显示出对酸的逆分数阶和逆一阶依赖性。添加卤化物离子和对甲苯磺酰胺(BAT的还原产物),溶剂介质离子强度的变化对速率没有影响。激活参数已评估。已经提出了与动力学数据一致的机理。单溴胺-T的质子化常数估计为29 +/-2。在钌(III)催化的反应中观察到Taft LFE关系,p * =-4.6,表明给电子基团提高了反应速率。在B = 355 K时观察到等速动力学关系,表明焓因子控制速率。 [参考:31]

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