Mechanistic Aspects of Ligand Substitution on the Cis-Diaqua-Chloro-Tris(Dimethyl Sulfoxide)Ruthenium(II) Complex by Some Sulfur-Containing Bioactive Ligands in Aqueous Medium

IF 2.1 4区 化学 Q3 CHEMISTRY, PHYSICAL
Animesh Chattopadhyay, A. Dey, P. Karmakar, S. Ray, D. Nandi, Roshni Sarkar(Sain), A. K. Ghosh
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引用次数: 0

Abstract

The synthesis and interactions of the cis-diaqua-chloro-tris(dimethyl sulfoxide)ruthenium(II) complex with selected sulfur-containing ligands such as 2-thiouracil, glutathione and L-cysteine have been studied by UV-Vis spectrophotometry in aqueous medium at pH 4.5. From experimental data it is clear that all three reactions proceed via two steps: the first one being a rate-limiting ligand-dependent replacement of one water molecule, followed by a ligand-independent ring closure step with the expulsion of the second water molecule. The substituted products have been characterised by Job's method, FTIR spectroscopy and electrospray ionisation mass spectrometry. Activation parameters (ΔH≠ and ΔS≠) and thermodynamic parameters (ΔH0 and ΔS0, from the temperature dependence of the outer-sphere association equilibrium constant) are presented. Consistent with the experimental findings, an associative interchange mechanism is proposed.
一些含硫生物活性配体在水介质中取代顺式-二水-氯-三(二甲基亚砜)钌(II)配合物的机理
用紫外-可见分光光度法研究了顺式二水-氯-三(二甲基亚砜)钌(II)配合物与2-硫脲嘧啶、谷胱甘肽和l -半胱氨酸等含硫配体在pH为4.5的水溶液中的合成及其相互作用。从实验数据可以清楚地看出,这三个反应都是通过两个步骤进行的:第一步是依赖配体的限速配体取代一个水分子,然后是不依赖配体的环闭合步骤,排出第二个水分子。取代产物用Job法、FTIR光谱和电喷雾质谱进行了表征。给出了活化参数(ΔH≠和ΔS≠)和热力学参数(ΔH0和ΔS0,由外球缔合平衡常数的温度依赖性得出)。与实验结果一致,提出了一种联想交换机制。
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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
5
审稿时长
2.3 months
期刊介绍: The journal covers the fields of kinetics and mechanisms of chemical processes in the gas phase and solution of both simple and complex systems.
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