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Synthesis,Characterization and Kinetics of Metal Complexes Containing Dithiocarbamate and Polypyridine

机译:含二硫代氨基甲酸酯和聚吡啶的金属配合物的合成,表征和动力学

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摘要

Complexes of the type [M(L)(ddtc)2],where M = Mn(II),Co(II),Ni(II),Cu(II) and Zn(II),L = 2,2'-bipyridine or 1,10-phenanthroline and ddtc = diethyldithiocarbamate,have been synthesized and characterized by elemental analyses,IR,electronic,EPR,H NMR spectral data,magnetic moment and conductivity measurements.The electrical conductivity of the complexes indicated them to be non-electrolyte in nitrobenzene.The spectroscopic evidences suggest that the complexes have an octahedral environment around the metal ion.Plot of log [LAMBDA_(infinity)/LAMBDA_(infinity)-LAMBDA_m] against time was linear suggesting first order kinetics of nucleophilic substitution of [Ni(bpy)(ddtc)2] by chloride ion in nitrobenzene.The results show that the rate of substitution is independent of the concentration of the nucleophile and depends only on the first power of the concentration of the complex.
机译:类型[M(L)(ddtc)2]的络合物,其中M = Mn(II),Co(II),Ni(II),Cu(II)和Zn(II),L = 2,2'-已合成并通过元素分析,红外,电子,EPR,1 H NMR光谱数据,磁矩和电导率测量对二吡啶或1,10-菲咯啉和ddtc =二乙基二硫代氨基甲酸酯进行了表征。配合物的电导率表明它们为非-光谱证据表明该络合物在金属离子周围具有八面体环境。对数对数[LAMBDA_(无穷大)/ LAMBDA_(无穷大)-LAMBDA_m]对时间的曲线是线性的,表明[Ni]的亲核取代具有一级动力学。 (bpy)(ddtc)2]在硝基苯中的氯离子。结果表明,取代速度与亲核试剂的浓度无关,并且仅取决于配合物浓度的一阶幂。

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