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首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Design, spectral characterization, DFT and biological studies of transition metal complexes of Schiff base derived from 2-aminobenzamide, pyrrole and furan aldehyde
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Design, spectral characterization, DFT and biological studies of transition metal complexes of Schiff base derived from 2-aminobenzamide, pyrrole and furan aldehyde

机译:由2-氨基苯甲酰胺,吡咯和呋喃醛衍生的席夫碱过渡金属配合物的设计,光谱表征,DFT和生物学研究

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A series of two biologically active Schiff base ligands L-1, L-2 have been synthesized in equimolar reaction of 2-aminobenzamide with pyrrol-2-carboxaldehyde and furan-2-carboxaldehyde. The synthesized Schiff bases were used for complexation with different metal ions like Co(II), Ni(II) and Cu(II) by using a molar ratio of ligand: metal as 2:1. The characterization of newly formed complexes was done by H-1 NMR, UV-Vis, TGA, IR, mass spectrophotomety, EPR and molar conductivity studies. The thermal studies suggested that the complexes are more stable as compared to ligand. In DFT studies the geometries of Schiff bases and metal complexes were fully optimized with respect to the energy using the 6-31+g(d,p) basis set. On the basis of the spectral studies an octahedral geometry has been assigned for Co(II) and Ni(II) complexes and distorted octahedral geometry for Cu(II) complexes. All the synthesized compounds, were studied for their in vitro antimicrobial activities, against four bacterial strains and two fungal strains by using serial dilution method. The data also revealed that the metal complexes showed better activity than the ligands due to chelation/coordination. (C) 2015 Elsevier B.V. All rights reserved.
机译:在2-氨基苯甲酰胺与吡咯-2-甲醛和呋喃-2-甲醛的等摩尔反应中,合成了一系列两个具有生物活性的席夫碱配体L-1,L-2。合成的席夫碱用于配体与金属的摩尔比为2:1,与不同的金属离子(例如Co(II),Ni(II)和Cu(II))络合。通过H-1 NMR,UV-Vis,TGA,IR,质谱,EPR和摩尔电导率研究对新形成的配合物进行表征。热学研究表明,与配体相比,配合物更稳定。在DFT研究中,使用6-31 + g(d,p)基集对Schiff碱和金属配合物的几何结构进行了能量方面的完全优化。根据光谱研究,已为Co(II)和Ni(II)配合物指定了八面体几何形状,为Cu(II)配合物指定了扭曲的八面体几何形状。使用连续稀释法研究了所有合成的化合物对四种细菌菌株和两种真菌菌株的体外抗菌活性。数据还显示,由于螯合/配位,金属配合物显示出比配体更好的活性。 (C)2015 Elsevier B.V.保留所有权利。

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