N-S供体Co (II)、Ni (II)和Cu (II)配合物的合成及其抑菌活性

Yogesh Kumar Gupta , Vinita Gupta , Sanchita Singh
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引用次数: 1

摘要

目的为了设计抗药微生物的新化合物,人们付出了极大的努力。正在进行的对新颖和惊人的药物输送系统的研究主要是由于一个公认的事实,即常规剂量在将药物化合物输送到其作用部位方面不够有效,这就需要寻找更有效的药物。在3%过氧化氢介质中,用双硫脲环化法制备了Co (II)、Ni (II)和Cu (II)与三齿配体2,5 -二氨基- 1,3,4 -噻二唑的金属配合物。2,5 -二氨基- 1,3,4 -噻二唑作为中性三齿配体,通过胺的硫原子和氮进行配位。配合物在DMF中是非电解质。配合物呈八面体几何。采用敏感性试验、最小抑制浓度法和最小细菌浓度法筛选配体及其配合物的抗菌活性。与对照和配体相比,金属螯合物表现出更强的抗菌活性。金属螯合物和配体对黑曲霉和青霉素没有活性。方法元素分析、红外光谱、法拉第天平磁化率、Genway 4200电导率仪摩尔电导。用α 4原子吸收分光光度计测定金属。采用硅胶包覆薄层色谱板进行薄层色谱。结果元素分析结果与公式计算结果吻合较好,分离得到1:2 (M:L)固体螯合物,其通式为[(ML2)] X2;M=Co (II), Ni (II)和Cu (II) (X=Cl)。红外光谱表明配体L为中性三齿配体。它通过胺和硫原子中的氮与金属离子配合。Co (II)、Ni (II)和Cu (II)配合物的摩尔电导值相对较低,表明这些配合物具有非电解性质。配体和金属配合物对除青霉素和曲霉霉菌外的被试生物物种均有抗菌作用。淋病奈瑟菌可能是对2,5 -二氨基- 1,3,4 -噻二唑及其金属配合物最敏感的生物。与母体化合物相比,金属配合物对某些微生物表现出更强的活性。结论化学和物理分析结果表明,配体(2,5 -二氨基- 1,3,4 -噻二唑)与Cu、Co、Ni配合。金属配合物具有比母体化合物更好的物理性能。2,5-二氨基-1,3,4-噻二唑金属配合物可能是一种较好的抗菌药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis and antimicrobial activities of Co (II), Ni (II) and Cu (II) complexes with N–S donor ligand

Aim

The extreme efforts have been developed to design novel compounds to strains of resistant micro-organisms. On-going search for novel and amazing drug delivery systems is primarily impact of the well-established fact that the convectional dosages are not sufficiently effective in conveying the drug compounds to its site of action and this has required the need to search for more efficient drugs. The metal complexes of Co (II), Ni (II) and Cu (II) with a tridentate ligand 2, 5-diamino-1, 3, 4-thiadiazole has been prepared by cyclisation of bithiourea in a 3% hydrogen peroxide medium. 2, 5-diamino-1, 3, 4-thiadiazole acts as neutral tridentate ligand and coordinates through the sulphur atom and nitrogen of the amines. The complexes are non-electrolyte in DMF. The complexes exhibited octahedral geometry. The antimicrobial activities of ligand and its complexes were screened using sensitivity test, minimum inhibition concentration and minimum bacterial concentration method. Metal chelates showed greater antimicrobial activities as compared to the control and the ligand. The metal chelates and the ligand did not exhibited activity against Aspergillus niger and Penicillin species.

Methods

Elemental analyses, IR spectra, magnetic susceptibilities by using Faraday Balance, molar conductance by using Genway 4200 conductivity meter. Metal estimation by using Alpha 4 Atomic Absorption Spectrophotometer. Thin layer chromatography was carried out using TLC plate coated with silica gel.

Results

The results of the elemental analyses are in good agreement with those calculated for the suggested formulae, 1:2 (M:L) solid chelates are isolated and found to have the general formulae [(ML2)] X2; M=Co (II), Ni (II) and Cu (II) (X=Cl). The IR spectra revealed that the ligand L is a neutral tridentate ligand. It coordinated to the metal ions via the nitrogen of the amines and sulphur atom. The molar conductance values of the Co (II), Ni (II), and Cu (II) complexes were relatively low, indicating the non-electrolytic nature of these complexes. The ligand and metal complexes show antimicrobial effect against the tested organism species except against molds of penicillin and Aspergillus. Niesseria gonorrhoea was probably the most sensitive organism to the 2, 5-Diamino-1, 3, 4-Thiadizole and its metal complexes. Metal complexes showed greater activity against some of the micro-organisms compared to the parent compounds.

Conclusion

In this paper we conclude from combined results of the chemical and physical analysis that the ligand (2, 5-diamino-1, 3, 4-thiadiazole) coordinated with Cu, Co and Ni. The metal complexes possess better physical properties than the parent compound. Metal complex of 2,5-diamino-1,3,4-thiadiazole would be a better therapeutic drug for antibacterial treatment.

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