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首页> 外文期刊>Journal of the Indian Chemical Society >A study on the arylazo coupling reaction of bis-(acetylacetone)ethylene-diaminocopper(II) and bis-(acetylacetone)ethylenediaminonickel(II)
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A study on the arylazo coupling reaction of bis-(acetylacetone)ethylene-diaminocopper(II) and bis-(acetylacetone)ethylenediaminonickel(II)

机译:双(乙酰丙酮)乙二氨基铜(II)与双(乙酰丙酮)乙二氨基镍(II)的芳偶氮偶合反应的研究

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摘要

The electrophilic substitution of aryl diazonium ion on the Cu~(II) and Ni~(II) chelates of bis-(acetylacetone)ethylenediamine [H4enacac] in aqueous medium have been studied.The coupling products were isolated and characterized by elemental analysis,magnetic susceptibility measurement and electronic,infrared,1H NMR,ESR and mass spectral studies.The parent chelates have undergone coupling at both the acetylacetone wings of the chelated ligand without decomposition.The geometry around the metal ion of the product is square planar as in the parent chelates.However a rearrangement is found occurred in the newly introduced azo group to hydrazone group followed by the coordination of its nitrogen to metal ion leaving the acetyl group free.As a result the coordination environment around the metal ion is changed from N2O2 to N4.
机译:研究了水介质中双-(乙酰丙酮)乙二胺[H4enacac]的Cu〜(II)和Ni〜(II)螯合物上芳基重氮离子的亲电取代。磁化率测量和电子,红外,1 H NMR,ESR和质谱研究。母体螯合物在螯合配体的两个乙酰丙酮翼上都经过偶联而没有分解。产物金属离子周围的几何形状像母体一样呈方形平面然而,在新引入的偶氮基团中发现重排为基团,然后氮与金属离子配位而使乙酰基自由,结果金属离子周围的配位环境从N2O2变为N4。

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