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由硫代碳酰肼和乙二醛衍生的大环配合物的模板合成、光谱研究及生物活性

Template synthesis, spectroscopic studies and biological activities of macrocyclic complexes derived from thiocarbohydrazide and glyoxal.

作者信息

Singh D P, Kumar Ramesh, Malik Vandna, Tyagi Parikshit

机构信息

Department of Chemistry, National Institute of Technology, Kurukshetra-136 119, India.

出版信息

J Enzyme Inhib Med Chem. 2007 Apr;22(2):177-82. doi: 10.1080/14756360601051399.

Abstract

A novel series of complexes of the type [M(TML)X2]; where TML is Tetradentate Macrocyclic Ligand; M = Co(II), Ni(II), Cu(II), Zn(II)or Cd(II); X = Cl-, CH3COO- or NO3- have been synthesized by template condensation of glyoxal and thiocarbohydrazide in the presence of divalent metal salts in methanolic medium. The complexes have been characterized by elemental analyses, conductance measurements, molecular weight determination, magnetic measurements, electronic, NMR, infrared and far infrared spectral studies. Electronic spectra along with magnetic moments suggest a six coordinate octahedral geometry for these complexes. The low molar conductance values indicates them to be non-electrolytes. The biological activities of the metal complexes have been tested in vitro against a number of pathogenic bacteria to assess their inhibitory potential.

摘要

一系列新型的[M(TML)X₂]型配合物已通过在甲醇介质中,在二价金属盐存在下,乙二醛和硫代碳酰肼的模板缩合反应合成,其中TML是四齿大环配体;M = Co(II)、Ni(II)、Cu(II)、Zn(II)或Cd(II);X = Cl⁻、CH₃COO⁻或NO₃⁻。这些配合物已通过元素分析、电导率测量、分子量测定、磁测量、电子、核磁共振、红外和远红外光谱研究进行了表征。电子光谱和磁矩表明这些配合物具有六配位八面体几何结构。低摩尔电导率值表明它们是非电解质。已对金属配合物的生物活性进行了体外测试,以评估它们对多种致病细菌的抑制潜力。

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