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Ferrocenyl-substituted Schiff base complexes of boron: Synthesis, structural, physico-chemical and biochemical aspects

机译:硼的二茂铁基取代的席夫碱配合物:合成,结构,物理化学和生物化学方面

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摘要

Biological important complexes of boron(III) derived from 1-acetylferrocenehydrazinecarboxamide (L~1H), 1- acetylferrocenehydrazinecarbothioamide (L2H) and 1-acetylferrocene carbodithioic acid (L~3H) have been prepared and investigated using a combination of microanalytical analysis, melting point, electronic, IR, ~1H NMR and ~(13)C NMR spectral studies, cyclic voltammetry and X-ray powder diffraction studies. Boron isopropoxide interacts with the ligands in 1:1, 1:2 and 1:3 molar ratios (boron:ligand) resulting in the formation of coloured products. On the basis of conductance and spectral evidences, tetrahedral structures for boron(III) complexes have been assigned. The ligands are coordinated to the boron(III) via the azomethine nitrogen atom and the thiolic sulfur atom/enolic oxygen atom. On the basis of X-ray powder diffraction study one of the representative boron complex was found to have orthorhombic lattice, having lattice parameters: a = 9.9700, b = 15.0000 and c = 7.0000. Both the ligands and their complexes have been screened for their biological activity on several pathogenic fungi and bacteria and were found to possess appreciable fungicidal and bactericidal properties. Plant growth regulating activity of one of the ligand and its complexes has also been recorded on gram plant, and results have been discussed.
机译:结合微分析,熔点的方法,研究了由1-乙酰基二茂铁羧酰胺(L〜1H),1-乙酰基二茂铁羰基硫代酰胺(L2H)和1-乙酰基二茂铁碳二硫酸(L〜3H)衍生的硼(III)的生物重要配合物。 ,电子,IR,〜1H NMR和〜(13)C NMR光谱研究,循环伏安法和X射线粉末衍射研究。异丙醇硼与配体的摩尔比为1:1、1:2和1:3(硼:配体),导致形成有色产物。根据电导和光谱证据,已确定了硼(III)配合物的四面体结构。配体通过甲亚胺氮原子和硫代硫原子/烯氧基氧原子与硼(III)配位。根据X射线粉末衍射研究,发现代表性的硼配合物之一具有正交晶格,其晶格参数为:a = 9.9700,b = 15.0000和c = 7.000。已经对配体及其配合物在几种致病真菌和细菌上的生物学活性进行了筛选,发现它们具有明显的杀真菌和杀菌特性。配体之一及其配合物的植物生长调节活性也已在革兰氏植物上记录,并讨论了结果。

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