首页> 外文期刊>International Journal of Pharmaceutical Sciences Review and Research >Synthesis, Characterization and In Vitro Antibacterial Evaluation of Sn, Sb, and Zn Coordination Complexes of 2-(2-Methoxyphenyl)-1H-Isoindole-1, 3(2h)-Dione
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Synthesis, Characterization and In Vitro Antibacterial Evaluation of Sn, Sb, and Zn Coordination Complexes of 2-(2-Methoxyphenyl)-1H-Isoindole-1, 3(2h)-Dione

机译:2-(2-甲氧基苯基)-1H-异吲哚-1,3(2h)-二酮的Sn,Sb和Zn配位化合物的合成,表征和体外抗菌评价

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Hunting of new biologically active compounds is the need of time. Thanks to metals for being the charm of this field since more than half a century. Present report describes the synthesis, chemistry and biological evaluation of metal complexes of N-aryl phthalimides, a very interesting class of compounds in terms of their wide biological and chemical applications. Ortho anisidine is reacted with phthalic anhydride under solvent free condition to give N-substituted aryl phthalimide (Ligand A). The resultant phthalimide is then reacted with different metals like alkyl Tin (IV) halides, Antimony (III), and Zinc (II) to form novel coordination complexes (C1-C7). All the synthesized compounds have been characterized by 1H NMR, 13C NMR, 119Sn NMR, FTIR, Mass spectrometry for m/z ratio. Fascinatingly, the synthesized complexes have shown improved antibacterial effects in comparison to their parent ligands against standard Ciprofloxacin.
机译:寻找新的生物活性化合物是需要时间的。由于金属在半个多世纪以来一直是该领域的魅力。本报告描述了N-芳基邻苯二甲酰亚胺金属络合物的合成,化学和生物学评估,这是一类非常有趣的化合物,具有广泛的生物学和化学用途。在没有溶剂的条件下,使邻茴香胺与邻苯二甲酸酐反应,得到N-取代的芳基邻苯二甲酰亚胺(配体A)。然后将所得邻苯二甲酰亚胺与不同的金属(如烷基锡(IV)卤化物,锑(III)和锌(II))反应以形成新型配位络合物(C1-C7)。所有合成的化合物已通过1H NMR,13C NMR,119Sn NMR,FTIR,质谱对m / z比进行了表征。令人着迷的是,与它们的母体配体相比,合成的复合物对标准环丙沙星具有更好的抗菌作用。

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