Synthesis, Spectroscopic, and Magnetic Studies of Mono- and Polynuclear Schiff Base Metal Complexes Containing Salicylidene-Cefotaxime Ligand

J. Anacona, Johan Calvo, O. Almanza
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引用次数: 17

Abstract

Metal complexes of a Schiff base ligand derived from cefotaxime and salicylaldehyde were prepared. The salicilydene-cefotaxime ligand (H2L) and mononuclear [M(L)] (M(II) = Co, Ni and Cu), dinuclear [Ag2(L)(OAc)2], and tetranuclear metal complexes [M4(L)(OH)6] (M(II) = Ni, Cu) were characterized on the basis of analytical, thermal, magnetic, and spectral studies (IR, UV-visible, 1H NMR, 13C NMR, and EPR). The electronic spectra of the complexes and their magnetic moments suggesttetrahedral geometry for the isolated complexes. The complexes are nonelectrolytes and insoluble in water and common organic solvents but soluble in DMSO.
含水杨苷-头孢噻肟配体的单核和多核希夫碱金属配合物的合成、光谱和磁性研究
以头孢噻肟和水杨醛为原料制备了席夫碱配体的金属配合物。通过分析、热、磁、光谱研究(IR、uv -可见、1H NMR、13C NMR和EPR)对水杨酸-铈肟配体(H2L)、单核[M(L)] (M(II) = Co、Ni和Cu)、双核[Ag2(L)(OAc)2]和四核金属配合物[M4(L)(OH)6] (M(II) = Ni、Cu)进行了表征。配合物的电子能谱及其磁矩表明,孤立配合物具有四面体的几何形状。该配合物为非电解质,不溶于水和普通有机溶剂,但可溶于二甲基亚砜。
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