Studies on Kinetics and Mechanism of Oxidation of GSH by cis-(diaqua)-bis-(ethylenediamine) Cobalt(III) Ion

Bijaylaxmi Mohanty, J. Behera, S. Acharya, P. Mohanty, A. Patnaik
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Abstract

The kinetics of GSH oxidation to GSSG by cis-(diaqua)-bis-(ethylenediamine) cobalt(III) perchlorate was studied spectophotometrically under pseudo-first order condition using 103[Co(III)] = 5 mol dm-3, 2.5 \(\le\) 102[GSH] \(\le\) 10.00 mol dm-3, 3.5 \(\le\) pH \(\le\) 5.0, 318K \(\le\) T \(\le\) 333K at a fixed ionic strength I = 0.3 mol dm-3 (NaClO4). The disappearance of [Co (III)] at 500 nm with time showed first-order kinetic trend. The first order dependence on [GSH] and pH was observed. Temperature dependence of the second order rate constant k'2 = kobs/[GSH] were analyzed for the Co(III)-OH23+(k1) and Co(III)-OH2+(k2) reactivities. An outer-sphere complex formation between the Co(III) and GSH followed by one-electron transfer from GSH to Co(III) resulting the formation of Co(II) and GSH radical. The GSH radical under- goes fast dimerisation to GSSG. Activation parameters were calculated. These values favor the electron transfer reaction. Negative value of activation entropy corresponds to ordered transition state.
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顺-(双水)-双-(乙二胺)钴(III)离子氧化谷胱甘肽的动力学及机理研究
在准一阶条件下,用103[Co(III)] = 5 mol dm- 3,2.5 \(\le\) 102[GSH] \(\le\) 10.00 mol dm- 3,3.5 \(\le\) pH \(\le\) 5.0, 318K \(\le\) T \(\le\) 333K,固定离子强度I = 0.3 mol dm-3 (NaClO4),用顺式(双水)-双-(乙二胺)钴(III)高氯酸盐氧化GSH生成GSSG的动力学研究。[Co (III)]在500 nm处随时间消失呈一级动力学趋势。观察到[GSH]和pH的一级依赖性。分析了Co(III)-OH23+(k1)和Co(III)-OH2+(k2)反应的二阶速率常数k′2 = kbs /[GSH]与温度的关系。Co(III)和GSH之间形成外球配合物,随后GSH向Co(III)转移一个电子,形成Co(II)和GSH自由基。GSH自由基快速二聚化成GSSG。计算活化参数。这些值有利于电子转移反应。激活熵为负值对应有序跃迁态。
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