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首页> 外文期刊>Progress in reaction kinetics and mechanism >Kinetics and mechanism of the ligand substitution reaction of di-μ-hydroxobis(bipyridyl)dipalladium(II) ion with dipeptides in aqueous solution
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Kinetics and mechanism of the ligand substitution reaction of di-μ-hydroxobis(bipyridyl)dipalladium(II) ion with dipeptides in aqueous solution

机译:水溶液中二μ-羟基双(联吡啶基)二钯(II)离子与二肽的配体取代反应的动力学和机理

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The interaction of the title complex with dipeptides such as glycylglycine (Gly - Gly) and glycylglutamine (Gly - Gln) has been studied spectrophotometrically in aqueous medium as a function of [substrate complex], [ligand] and temperature at a particular pH (7.4), where the substrate complex exists predominantly as the dimeric dihydroxo-bridged species and the dipeptides are in zwitterionic form, at constant ionic strength. The reactions have been studied under pseudo-first order conditions. The reaction proceeds in a two-step-consecutive manner (A → B → C); where the first step is ligand-dependent and second step is ligand-independent, and is assigned to ring closure. Based on the kinetic and activation parameters, an associative interchange mechanism is proposed for the interaction processes.
机译:在水介质中,分光光度法研究了标题配合物与二肽如甘氨酰甘氨酸(Gly-Gly)和甘氨酰谷氨酰胺(Gly-Gln)的相互作用,该作用是[底物配合物],[配体]和温度在特定pH(7.4 ),其中底物络合物主要以二聚体的二羟基桥连形式存在,而二肽为两性离子形式,且离子强度恒定。已经在拟一级反应条件下研究了反应。反应以两步连续的方式进行(A→B→C)。其中第一步是配体依赖性的,而第二步是配体依赖性的,并分配给闭环。基于动力学参数和激活参数,提出了一种相互作用过程的关联互换机制。

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