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Synthesis, spectral, and biological studies of transition metal chelates of N-[1-(3-aminopropyl)imidazoIe]salicylaldimine

机译:N- [1-(3-氨基丙基)咪唑基]水杨醛亚胺的过渡金属螯合物的合成,光谱和生物学研究

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摘要

Tridentate chelate complexes M[LX-2H_2O], where M = Co(II), Ni(II), Cu(II), Zn(II), and Cd(II) have been synthesized from the Schiff base L = N-[1-(3-aminopropyl)imidaz-ole]salicylaldimine and X = C1. Microanalytical data, UV-Vis, magnetic susceptibility, IR, 'H-NMR, mass, and EPR techniques were used to confirm the structures. Electronic absorption spectra and magnetic susceptibility measurements suggest square-planar geometry for copper complex and octahedral for other metal complexes. EPR spectra of copper(II) complex recorded at 300 K confirm the distorted square-planar geometry of the copper(II) complex. Biological activities of the ligand and metal complexes have been studied on Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, and Candida albicans by the well diffusion method. The activity data show the metal complexes to be more potent than the parent ligand against two bacterial species and one fungus. The electrochemical behavior of the copper complex was studied by cyclic voltammetry.
机译:由席夫碱合成的三齿螯合物M [LX-2H_2O],其中M = Co(II),Ni(II),Cu(II),Zn(II)和Cd(II)。 1-(3-氨基丙基)咪唑-ole]水杨醛亚胺,X = C1。微观分析数据,UV-Vis,磁化率,IR,1 H-NMR,质量和EPR技术用于确认结构。电子吸收光谱和磁化率测量表明,铜配合物为正方形平面几何形状,其他金属配合物为八面体形状。在300 K处记录的铜(II)配合物的EPR光谱证实了铜(II)配合物的扭曲的方平面几何形状。已经通过井扩散法研究了金黄色葡萄球菌,大肠杆菌,铜绿假单胞菌和白色念珠菌对配体和金属配合物的生物活性。活性数据表明,金属配合物对两种细菌和一种真菌的抵抗力大于母体配体。通过循环伏安法研究了铜配合物的电化学行为。

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