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Syntheses physicochemical characterization antibacterial studies on potassium morpholine dithiocarbamate nickel (II) copper (II) metal complexes and their ligands

机译:吗啉二硫代氨基甲酸钾镍(II)铜(II)金属配合物及其配体的合成理化性质和抗菌研究

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摘要

Organic molecule dithiocarbamate transition metal complexes are novel and very attractive pharmaceutical targets for the management and control of antibiotic resistant bacteria. The direct reaction has synthesized new transition metal nickel (II), copper (II) complexes of potassium morpholine dithiocarbamate (K+C5H8NOS2) ligands and characterized by UV-visible spectroscopy, Fourier-transform infrared spectroscopy (FTIR), as well as NMR physicochemical techniques. Antibacterial bioefficacy of the ligand and its metal complexes has been investigated in vitro on the growth of Gram-positive (Staphylococcus aureus MTCC 737, Bacillus cereus MTCC 1272) and the Gram-negative (Listeria monocytogenes MTCC 657, Shigella flexeneri MTCC 1457) bacteria. The obtained electronic spectral bands are characteristic and consistent with the proposed composition of the ligand as well as its metal complexes. It also provides a further example of the bidentate coordination of dithiocarbamate ligands. Absorption peak values of FTIR are characteristic of the ligand as well as dithiocarbamate group molecules and exhibit their metal coordination. NMR 1H signal variations also correlate with the coordination mediated chemical shifts. Both the metal complexes showed significant antibacterial activity. However, enhanced antimicrobial activity of the ligands than metal complexes against Gram positive and Gram negative bacteria were observed. Thus, further study on this approach could pave a way for the development of dithiocarbamate-metal complex based antibacterial agent.
机译:有机分子二硫代氨基甲酸酯过渡金属配合物是新型且非常有吸引力的药物靶标,用于管理和控制抗生素抗性细菌。直接反应合成了吗啉二硫代氨基甲酸钾(K + C5H8NOS2 -)配体的新型过渡金属镍(II),铜(II)配合物并通过紫外可见光谱进行了表征,傅立叶变换红外光谱(FTIR)以及NMR物理化学技术。在体外研究了配体及其金属配合物对革兰氏阳性菌(金黄色葡萄球菌MTCC 737,蜡状芽孢杆菌MTCC 1272)和革兰氏阴性菌(单核细胞增多性李斯特菌MTCC 657,屈氏志贺氏菌MTCC 1457)细菌的体外抗菌作用。获得的电子光谱带是特征性的,并且与所提出的配体及其金属配合物的组成一致。它还提供了二硫代氨基甲酸酯配体的双齿配位的另一个例子。 FTIR的吸收峰是配体以及二硫代氨基甲酸酯基团分子的特征,并表现出它们的金属配位。 NMR 1 H信号的变化也与配位介导的化学位移有关。两种金属配合物均显示出显着的抗菌活性。然而,观察到与金属配合物相比,配体对革兰氏阳性和革兰氏阴性细菌的抗菌活性增强。因此,对该方法的进一步研究可为开发基于二硫代氨基甲酸酯-金属配合物的抗菌剂铺平道路。

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