h-吲哚-2,3-二酮与肼碳硫酰胺衍生的希夫碱钴(ii)和镍(ii)配合物的合成、光谱测定和体外抗菌研究

S. Isyaku, J. Bello, H.N. Aliyu, T. Abubakar, M. Imam
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摘要

h -吲哚-2,3-二酮与肼碳硫酰胺缩合得到席夫碱(2Z)-2-(2-羟基- 3h -吲哚-3-基乙基肼- 1-碳硫酰胺。通过金属(II)盐与合成的希夫碱相互作用,制备了钴(II)和镍(II)配合物。采用磁化率、摩尔电导、红外光谱、原子吸收光谱、溶解度吸光度和实验式对所制化合物进行了分析。配合物的分解温度适中。希夫碱及其配合物的红外光谱数据表明,希夫碱与金属(II)离子通过亚甲基氮、吲哚氧和硫硫进行配位。配合物的有效磁矩显示为八面体几何。摩尔电导率表明这些配合物具有非电解性质。吸光度和经验公式的结果表明,希夫碱对金属离子的性质是单碱和三叉碱。筛选了配体和配合物对金黄色葡萄球菌、鼠伤寒沙门菌、大肠杆菌的抑菌活性;黄曲霉、烟曲霉和毛霉(indicus种)(真菌)。以阿莫西林和酮康唑分别作为细菌和真菌分离物的阳性对照。结果表明,配合物的活性高于游离配体,但低于标准配体。
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Synthesis, spectroscopic determination and in vitro antimicrobial studies of cobalt(ii) and nickel(ii) complexes of a Schiff base derived from 1h-indole-2,3- dione with hydrazinecarbothioamide
Condensation of H-Indole-2,3-dione with Hydrazinecarbothioamide produced a Schiff base (2Z)-2-(2-Hydroxy-3H-indol-3- ylidinehydrzinE- 1-Carbothioamide. Cobalt(II) and Nickel(II) complexes, were prepared by the interaction of the metal(II) salts with the synthesized Schiff base. The prepared compounds were analysed by magnetic susceptibility, molar conductance, FTIR, AAS, solubility absorbance and empirical formula. The complexes showed moderate values of decomposition temperatures. Infrared spectral data of the Schiff base and the complexes, indicated coordination of the Schiff base to the metal(II) ions via azomethine nitrogen, indole oxygen and thione sulphur. The effective magnetic moment of the complexes suggested an octahedral geometry. The molar conductivities indicated a non- electrolytic nature of these complexes. The results of the absorbance and the empirical formula showed that, the Schiff base is monobasic and tridentate in nature towards the metal ions. Both the ligand and the complexes were screened for antimicrobial activity against Staphylococcus aureus, Salmonella typhimurium, Escherichia coli (bacteria); Aspergillus flavus, Aspergillus fumigatus and Mucor (indicus species) (fungi). Amoxicillin and Ketoconazole were used as positive control for the bacteria and fungi isolates respectively. The results showed that the complexes are more active than the free ligand but less active when compared with the standards.
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