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首页> 外文期刊>Journal of Molecular Structure >Syntheses of and structural studies on some square planar dithiophosphonato Ni(II) complexes, octahedral pyridine derivatives thereof and X-ray crystallography, DFT and molecular docking studies of the latter
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Syntheses of and structural studies on some square planar dithiophosphonato Ni(II) complexes, octahedral pyridine derivatives thereof and X-ray crystallography, DFT and molecular docking studies of the latter

机译:一些方形平面二硫代磷酸钠Ni(II)复合物,八面体吡啶衍生物及其X射线结晶,DFT和分子对接研究后者的合成及结构研究

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Five new dithiophosphonic acids ((p-MeO-C6H4)PS(SH)(OR), HLn, (n = 1-5); R = 3-pentyl-, HL1; R = 1-phenyl-1-propyl-, HL2; R = 4-tert-butyl benzyl-, HL3; R = diphenylmethyl-, HL4; R=4-tert-butylcyclohexyl-, HL5) were prepared by the reaction of Lawesson reagent with the corresponding alcohols. As the acids were viscous liquids and difficult to purify they were converted to their ammonium salts ([NH(4)Ln]) for purification through crystallization. Four coordinated Ni(II) complexes of the dithiophosphonates ([Ni(Ln)(2)]) were synthesized in methanol medium and purified. The reaction between these square planar complexes and pyridine was carried out to produce six coordinated pyridine derivatives ([Ni(Ln)(2)(py)(2)]). The structures of the fifteen compounds so prepared were elucidated by spectroscopy, elemental analysis methods and magnetic susceptibility measurement. The molecular and crystal structure of [Ni(L2)(2)(py)(2)] was determined by X-ray crystallography. DFT calculations were carried out using the B3LYP functional with the LANL2DZ basis set to the optimized geometrical structure and determine the energies, the orientations of the molecular orbitals (HOMOs and LUMOs) and the molecular electrostatic potential (MEP) surfaces of the octahedral complex [Ni(L2)(2)(py)(2)]. The results for [Ni(L2)(2)(py)(2)] revealed that these bonded to the active sites of A-DNA and B-DNA by weak non-covalent interactions, which was also supported by molecular docking investigations. (C) 2018 Elsevier B.V. All rights reserved.
机译:五种新的二硫代膦酸((p-meo-c6h4)ps(sh)(或),hln(n = 1-5); r = 3-戊基 - ,hl1; r = 1-苯基-1-丙基, HL2; r = 4-叔丁基苄基 - ,HL 3; r =二苯基甲基 - ,HL4; r = 4-叔丁基环己基 - ,HL5)通过对应的相应醇的反应来制备。由于酸是粘性液体,并且难以净化它们,将它们转化为其铵盐([NH(4)LN])通过结晶纯化。在甲醇培养基中合成了二硫代膦酸盐([Ni(LN)(2)])的四个配位Ni(II)复合物并纯化。进行这些方形平面复合物和吡啶之间的反应,以产生六个配位的吡啶衍生物([Ni(Ln)(2)(Py)(2)])。通过光谱学,元素分析方法和磁性敏感性测量阐明了如此制备的十五种化合物的结构。 [Ni(L2)(2)(2)(Py)]的分子和晶体结构由X射线晶体学确定。使用B3Lyp功能与LANL2DZ基础设定为优化的几何结构并确定能量,分子轨道(HOMOS和LUMOS)的方向和八面体复合物的分子静电电位(MEP)表面的能量[Ni (L2)(2)(PY)(2)]。 [Ni(L2)(2)(2)(2)]的结果表明,通过弱的非共价相互作用,这些键合到A-DNA和B-DNA的活性位点,其也得到了分子对接研究的支持。 (c)2018年elestvier b.v.保留所有权利。

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