Co(III)、Fe (III)和Cr(III) Salen Schiff碱配合物催化l -半胱氨酸氧化的动力学和机理

H. Abdel-Halim, H. Baker, Akef I. Alhmaideen, A. Abu-Surrah
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摘要

[MIII(L)Cl] (M = Co, Fe, Cr)新系列取代onno供体salen型席夫碱配合物氧化L-半胱氨酸的动力学L =希夫碱配体)在水溶液中的研究。在恒温(25ºC)、离子强度恒定(0.20 M)和pH恒定(7.0)的准一阶条件下进行测量,其中半胱氨酸的浓度比金属配合物的浓度大两个数量级。观察到的速率常数是通过跟踪反应混合物在预定波长的吸光度随时间的变化来确定的。结果表明,Co(III)配合物的氧化速率与金属中心类型有关,由于Co(III)的还原电位较高,其氧化速率最高。氧化速率还取决于空间因子和与金属离子结合的配体的吸/释放电子的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Kinetics and Mechanism of Catalyzed Oxidation of L-Cysteine by Salen Schiff Base Complexes of Co(III), Fe (III) and Cr(III)
Kinetics of oxidation of L-cysteine by new series of substituted ONNO-donor salen-type Schiff base complexes of general formula [MIII(L)Cl] (M = Co, Fe, Cr; L = Schiff base ligand) have been studied in aqueous solutions. Measurements were run at constant temperature (25º C), constant ionic strength (0.20 M), and constant pH (7.0) under pseudo-first order conditions, in which the concentration of cysteine is around two orders of magnitude greater than that of metal complex. The observed rate constant was determined by following the change in absorbance of reaction mixture at a predetermined wavelength with time. Results show that the rate of oxidation depends on the type of metal center, with Co(III) complexes were found to have the highest rates due to higher reduction potential of Co(III). The oxidation rate was also found to depend on steric factor and the electron withdrawing / releasing ability of the ligand bound to the metal ion.
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