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Synthesis and biological activity of a ferrocenyl ligand derived from thiophenol and its coordination with some transition metals

机译:硫酚衍生的二茂铁基配体的合成,生物活性及其与某些过渡金属的配位

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摘要

The new ferrocenyl ligand 1,1'-bis(2,3-dihy-dro-2-methylbenzo[d]thiazol-2-yl)ferrocene was prepared at room temperature from the condensation reaction of 2-aminothiophenol with 1,1'-diacetylferrocene followed by intramolecular Michael-type addition. The prepared ligand forms 1:1 complexes with manganese(II), cobalt(II), nickel(II), copper(II), and zinc(II) in good yield. Characterization of the ligand and its complexes was carried out using IR, ~1H and ~(13)C NMR, electronic absorption, mass spectra, magnetic susceptibility, molar conductance, and elemental analysis. Biological activity of the ligand and its complexes was assessed against Bacillus subtilis, Staphylococcus aureus, Escherichia coli, Alcaligenes faecalis, Aspergillus niger, and Candida albicans. The results indicated that the ligand is biologically active but the complexes are more active. The Zn and Cu complexes exhibited biological activity comparable to that of chloramphenicol (commercial broad-spectrum antibiotic).
机译:在室温下,由2-氨基硫酚与1,1'的缩合反应制备了新的二茂铁基配体1,1'-双(2,3-二氢-dro-2-甲基苯并[d]噻唑-2-基)二茂铁-二乙酰基二茂铁,然后进行分子内迈克尔型加成。制备的配体与锰(II),钴(II),镍(II),铜(II)和锌(II)形成1:1的配合物,收率很高。使用IR,〜1H和〜(13)C NMR,电子吸收,质谱,磁化率,摩尔电导和元素分析对配体及其配合物进行表征。评估了该配体及其复合物对枯草芽孢杆菌,金黄色葡萄球菌,大肠杆菌,粪便产碱杆菌,黑曲霉和白色念珠菌的生物活性。结果表明,配体具有生物活性,但复合物具有更高的活性。锌和铜配合物的生物活性与氯霉素(商业广谱抗生素)相当。

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