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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >CRYSTAL STRUCTURE AND THIRD-ORDER NONLINEARITY OF NICKEL(II) AND COPPER(II) COMPLEXES WITH S-METHYL BETA-N-(4-NITROBENZAL)METHYLENEDITHIOCARBAZATE
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CRYSTAL STRUCTURE AND THIRD-ORDER NONLINEARITY OF NICKEL(II) AND COPPER(II) COMPLEXES WITH S-METHYL BETA-N-(4-NITROBENZAL)METHYLENEDITHIOCARBAZATE

机译:镍(II)和铜(II)与β-甲基β-N-(4-硝基苯)甲基碳酸二甲酯的络合物的晶体结构和三阶非线性

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摘要

Ni-II and Cu-II complexes of general formula ML2 [HL = S-methyl-beta-N-(nitrobenzal)methylene- dithiocarbazate] have been synthesized and characterized. The Schiff base acts as a single, negatively charged bidentate ligand forming extensive electron delocalization system. Single crystal X-ray diffraction analysis of the copper(II) complex revealed that the ligand lost a proton from its tautomeric thiol form and coordinates to Cu-II via mercapto sulfur and beta-nitrogen atoms. The geometry of the Cu-II ion is square-planar with two equivalent Cu--S and Cu--N bonds. The two nitrobenzal rings and the coordinated moieties are almost in one plane, forming an electronic delocalization system. Third-order response-determinations show that the extensive electron delocalization is quite helpful for the complexes exhibit higher second order molecular hyperpolarizability. Crystal structure of the free ligand is also determined for comparison. (C) 1997 Elsevier Science Ltd. [References: 27]
机译:合成并表征了通式为ML2的Ni-II和Cu-II配合物[HL = S-甲基-β-N-(硝基苯甲醛)亚甲基-二硫代氨基甲酸酯]。席夫碱作为单个带负电荷的二齿配体,形成大量的电子离域系统。铜(II)配合物的单晶X射线衍射分析表明,该配体从其互变异构硫醇形式失去质子,并通过巯基硫和β-氮原子与Cu-II配位。 Cu-II离子的几何形状为正方形平面,带有两个等效的Cu-S和Cu-N键。两个硝基苯环和配位部分几乎在一个平面上,形成电子离域系统。三阶响应测定表明,广泛的电子离域非常有助于配合物表现出更高的二阶分子超极化能力。还确定了游离配体的晶体结构用于比较。 (C)1997 Elsevier Science Ltd. [参考:27]

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