Oxidation of Thioglycolic Acid by Nickel(IV) Oxime-Imine Complexes - A Kinetic and Mechanistic Approach

S. Bhattacharya, A. Dutta, P. Banerjee
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引用次数: 2

Abstract

Abstract The kinetics of oxidation of thioglycolic acid (H2A) by two nickel(IV) oxime-imine complexes, [NiIV(L1)2]2 + and [NiIV(L2)]2+ (where HL1 and H2L2 are 6-amino-3-methyl-4-azahex-3-ene-2-one oxime and 3,14-dimethyl-4,7,10,13-tetraazahexadeca-3,13- diene-2,15-dione dioxime respectively) were carried out by using stopped-flow technique in the pH range 3.0-8.0. Under pseudo-first-order conditions the reaction follows a general rate law: - (d/dt) [Ni(Lx)] =kobs [Ni(Lx)] = nk [Ni(Lx)] [H2A]T where n is the stoichiometric factor with 0.5 for NiIV → NIII reactions and 1 for each step of Ni IV→ NiIII → NiII biphasic conversions. The evaluation of rate and equilibrium constants of the reactants was achieved by employing suitable computer-fit programs. Both the reactions have been proposed to follow the inner-sphere mechanism through the formation of an associated species involving the sulfur atom of the thiol and the metal center of the oxidant.
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镍(IV)肟-亚胺配合物氧化巯基乙酸的动力学和机理研究
摘要在pH 3.0 ~ 8.0范围内,采用停流技术研究了两种镍(IV)肟-亚胺配合物[NiIV(L1)2]2 +和[NiIV(L2)]2+(其中HL1和H2L2分别为6-氨基-3-甲基-4-氮杂蒽-3-烯-2-酮肟和3,14-二甲基-4,7,10,13-四氮杂蒽-3,13-二烯-2,15-二酮二肟)对巯基乙酸(H2A)的氧化动力学。在拟一阶条件下,反应遵循一般速率规律:- (d/dt) [Ni(Lx)] =kobs [Ni(Lx)] = nk [Ni(Lx)] [H2A]T,其中n为化学计量因子,NiIV→NIII反应为0.5,NiIV→NiIII→NIII双相转化每一步为1。用合适的计算机拟合程序计算了反应物的速率常数和平衡常数。这两种反应都遵循内球机制,通过形成涉及硫醇的硫原子和氧化剂的金属中心的伴生物质。
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