含异烟肼双齿希夫碱的Cu(II)、Ni(II)和Zn(II)混合配体配合物的合成、表征及其抗菌和抗氧化活性

Md. Ashrafuzzaman, Farzana Khanm Camellia, Md. Hafijur Rahman, Md. Delwar Hossain, Md. Tanvir Hossain, Hafizur Rahman, Md. Golam Mostafiz Shovon, Gobindo Kumar Paul, Md. Kudrat-E-Zahan, Md. Masuqul Haque
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摘要

本文合成了L1、L2、L1 = N-(4-甲氧基苄基)异烟碱腙、L2 = 2-氨基苯酚及其金属(Cu2+、Ni2+和Zn2+)配合物,并采用电导率、磁化率、红外光谱和紫外可见光谱等分析和物理化学技术对其进行了表征。根据摩尔电导测量,所有金属配合物都是1:1的电解质。红外光谱研究表明,配体通过亚甲基氮原子和羰基氧原子的N和O给体位点与相应的金属离子配位。磁矩和紫外可见光谱数据证实了Cu(II)和Ni(II)配合物为正方形平面结构,Zn(II)离子配合物为四面体结构。从L1和L2衍生的金属配合物对大肠杆菌和假单胞菌进行了抑菌活性测试,其中Cu(II)配合物对对照药物卡那霉素-30的抑菌活性高于这两种细菌。此外,所合成的金属配合物表现出比希夫碱中等的抗氧化活性。与BHT相比,Cu(II)配合物的抗氧化活性最高,Zn(II)配合物的抗氧化活性最低。
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Synthesis, Characterization, Antibacterial and Antioxidant Activities of Cu(II), Ni(II), and Zn(II) Mixed Ligand Complexes Containing Isoniazid Based Bidentate Schiff Base
Two mixed ligands (L1, L2), L1 = N-(4-methoxybenzylidene) isonicotinohydrazone, L2 = 2-aminophenol, and their metal (Cu2+, Ni2+, and Zn2+) complexes with stoichiometry (1:1:1) were synthesized and characterized by analytical and physico-chemical techniques such as conductivity, magnetic susceptibility measurements, IR-spectra, and UV-Visible spectra. All of the metal complexes were 1:1 electrolyte, according to the molar conductance measurements. It can be concluded from the IR study that the ligands were coordinated to the corresponding metal ions through N and O donor sites of the azomethine nitrogen atom and the carbonyl oxygen atom. Magnetic moment and UV-Vis spectra data confirmed that square planar geometry for Cu(II) and Ni(II) complexes, and tetrahedral structure for Zn(II) ion complex. The metal complexes derived from L1 and L2 were tested against Escherichia coli and Pseudomonas sp. Among the tested compounds, Cu(II) complex showed higher antibacterial activity over both bacterial strains against reference drug Kanamycin-30. Moreover, synthesized metal complexes exhibited moderate antioxidant activity than the Schiff base. Cu(II) complex was found to be most active whereas, Zn(II) complex showed the lowest antioxidant activity comparable to the BHT.
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