N-(4-羟基苄基)异烟碱腙过渡金属配合物的合成、表征、热研究及其抗菌抗氧化性能研究

F. Camellia, M. Ashrafuzzaman, Md. Nazrul Islam, L. Banu, M. Kudrat-E-Zahan
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引用次数: 0

摘要

合成了席夫碱配体N-(4-羟基苄基)异烟碱腙(L1)的Cr3+、Co2+、Ni2+、Cu2+和Zn2+离子配合物,并采用电导率、磁化率、红外光谱、紫外可见分光光度法和热重分析(TGA)等分析和物理化学方法对其进行了表征。红外数据显示L1呈双齿状。IR、TGA、磁矩测量和UV-Vis光谱数据证实了Cr3+、Co2+和Cu2+离子配合物为八面体结构,Ni2+离子配合物为正方形平面结构,Zn2+离子配合物为四面体结构。研究了L1配体衍生的金属配合物对铜绿假单胞菌和大肠杆菌的抑菌活性。与标准卡那霉素-30相比,所有合成的配合物对铜绿假单胞菌均表现出较强的抗菌效果,其中Ni2+配合物的抗菌效果最好。另一方面,与所有化合物相比,Zn2+配合物对大肠杆菌具有较强的抗菌作用。此外,合成的金属配合物比L1具有中等的抗氧化活性。抗氧化活性依次为BHT > CuL1 > CrL1 > NiL1 > CoL1 > ZnL1 > L1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis, Characterization and Thermal Study of Some Transition Metal Complexes of N-(4-hydroxybenzylidene)isonicotinohydrazone and Investigation of Their Antibacterial and Antioxidant Properties
Cr3+, Co2+, Ni2+, Cu2+ and Zn2+ ions complexes of the Schiff base ligand, N-(4-hydroxybenzylidene)isonicotinohydrazone (L1), were synthesized and characterized by analytical and physicochemical techniques including conductivity measurements, magnetic susceptibility measurements, IR Spectroscopy, UV-Visible Spectrophotometry and thermogravimetric analysis (TGA). IR data revealed the bidentate nature of the L1. IR, TGA, Magnetic moment measurements and UV-Vis spectra data confirmed the octahedral geometry for the Cr3+, Co2+, and Cu2+ ion complexes, square planar geometry for the Ni2+ complex and tetrahedral structure for the Zn2+ ion complex. The antibacterial activity of the metal complexes derived from the L1 ligand were tested against P. aeruginosa and E. coli. All produced complexes demonstrated strong antibacterial efficacy against P. aeruginosa when compared to standard Kanamycin-30, with the greatest for the Ni2+ complex. On the other hand, when compared to all compounds, the Zn2+ complex demonstrated strong antibacterial efficacy against E. coli. Furthermore, the synthesized metal complexes exhibited moderate antioxidant activity than the L1. The antioxidant activity was found to follow the following sequence: BHT > CuL1 > CrL1 > NiL1 > CoL1 > ZnL1 > L1.
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