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首页> 外文期刊>MedChemComm >Synthesis, antibacterial evaluation and QSAR analysis of Schiff base complexes derived from [2,2 '-(ethylenedioxy)bis(ethylamine)] and aromatic aldehydes
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Synthesis, antibacterial evaluation and QSAR analysis of Schiff base complexes derived from [2,2 '-(ethylenedioxy)bis(ethylamine)] and aromatic aldehydes

机译:[2,2'-(乙二氧基)双(乙胺)]与芳香醛衍生的席夫碱配合物的合成,抗菌评价和QSAR分析

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摘要

Two new Schiff bases derived from 1-hydroxy-2-naphthaldehyde/2-hydroxy benzaldehyde with 2,2'-(ethylenedioxy)bis(ethylamine) and their organosilicon and organotin complexes have been synthesized and characterized by spectroscopic techniques (UV-vis, IR and NMR) in combination with elemental analyses. Spectroscopic studies suggest bonding between the central atom and ligands in a penta and hexacoordinated fashion. Derived complexes and their corresponding ligands were evaluated for their antibacterial activity against Gram positive bacteria viz. Staphylococcus epidermidis, Staphylococcus hominis and Gram negative bacteria viz. Pseudomonas aeruginosa and Klebsiella pneumoniae and this study revealed that compounds 29, 30 and 34 exhibited antibacterial activities even better than the standard drug ciprofloxacin. For most of the complexes, higher activity was observed on coordination with silicon and tin atoms compared to their respective ligands. Compounds 1-34 were selected for the QSAR analysis in order to correlate antibacterial activity with significant structural parameters. The statistical parameters used were Dipole, HOMO, CVolume and Total Energy.
机译:已通过光谱技术(UV-vis, IR和NMR)结合元素分析。光谱学研究表明中心原子和配体之间的结合以五元和六配位方式存在。评价衍生的复合物及其相应的配体对革兰氏阳性细菌的抗菌活性。表皮葡萄球菌,人型葡萄球菌和革兰氏阴性菌即。铜绿假单胞菌和肺炎克雷伯菌和这项研究表明,化合物29、30和34表现出的抗菌活性甚至比标准药物环丙沙星好。对于大多数配合物,与它们各自的配体相比,在与硅和锡原子配位时观察到更高的活性。选择化合物1-34进行QSAR分析,以使抗菌活性与重要的结构参数相关联。使用的统计参数是偶极子,HOMO,C体积和总能量。

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