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Palladium(II)-catalyzed oxidation of tranexamic acid by bromamine-B in alkaline medium and uncatalyzed reaction in acid medium: A study of kinetic and mechanistic chemistry

机译:钯(II)催化溴化氨基乙酸在碱性介质中氧化氨甲环酸和在酸性介质中的非催化反应:动力学和机械化学研究

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摘要

Tranexamic acid (TA) possess antifibrinolytic properties and finds extensive applications in pharmaceuticals. Its oxidation-kinetic study is of much significance in understanding the mechanistic profile of TA in biological systems. In this context, a systematic kinetic study of palladium(II) (Pd(II)) catalyzed oxidation of TA by sodium N-bromobenzenesulfonamide or bromamine-B (BAB) in alkaline medium and uncatalyzed reaction in perchloric acid medium at 303 K was investigated. In acid medium, the reaction exhibits a first-order dependence of rate on BABo and less than unity order dependence on TAo. The reaction rate shows inverse less than unity order dependence with respect to H+. In alkaline medium, the reaction shows first-order dependence on both BABo and Pd(II) and zero-order with respect to TAo. The order with respect to OH - is less than unity. Activation parameters have been evaluated. The oxidation reactions are nearly 10-fold faster in acid medium in comparison with alkaline medium. In alkaline medium, the Pd(II) catalyzed reactions are about 6-fold faster than the uncatalyzed reaction. Further, the catalytic constant (KC) has been calculated at different temperatures and activation parameters with respect to Pd(II) catalyst have also been evaluated. The conjugate acid C6H5SO2NHBr and the anion C 6H5SO2N-Br of BAB have been postulated as the reactive oxidizing species in acid and alkaline media, respectively. The proposed mechanisms and derived rate laws are in agreement with the observed kinetics. © 2010 Elsevier B.V. All rights reserved.
机译:氨甲环酸(TA)具有抗纤维蛋白溶解特性,并在药物中得到广泛应用。它的氧化动力学研究对理解生物系统中TA的机理具有重要意义。在此背景下,系统地研究了钯(II)(Pd(II))在碱性介质中被N-溴苯磺酰胺钠或溴胺-B(BAB)催化TA氧化以及在303 K的高氯酸介质中未催化反应的动力学。 。在酸性介质中,反应对BABo的反应速率呈一阶依赖性,对TAo的反应小于一阶依赖性。反应速率显示出相对于H +小于一阶依赖关系。在碱性介质中,反应显示出对BABo和Pd(II)的一阶依赖性以及相对于TAo的零阶依赖性。关于OH-的顺序小于1。激活参数已评估。与碱性介质相比,在酸性介质中的氧化反应快近10倍。在碱性介质中,Pd(II)催化的反应比未催化的反应快约6倍。此外,已经在不同温度下计算了催化常数(KC),并且还评估了相对于Pd(II)催化剂的活化参数。假设BAB的共轭酸C6H5SO2NHBr和阴离子C 6H5SO2N-Br分别在酸性和碱性介质中作为反应性氧化物质。拟议的机制和派生的速率定律与观察到的动力学一致。 ©2010 Elsevier B.V.保留所有权利。

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