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首页> 外文期刊>Transition Metal Chemistry >Synthesis, properties, and crystal structures of mononuclear nickel(II) and copper(II) complexes with 2-oximino-3-thiosemicarbazone-2,3-butanedione
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Synthesis, properties, and crystal structures of mononuclear nickel(II) and copper(II) complexes with 2-oximino-3-thiosemicarbazone-2,3-butanedione

机译:单核镍(II)和铜(II)与2-氧亚氨基-3-硫代半碳酮-2,3-丁二酮配合物的合成,性质和晶体结构

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摘要

The tridentate ligand 2-Oximino-3-thiosemicarbazone-2,3-butanedione (Hotsb) reacts with MCl2 (M = Ni2+ or Cu2+) to give rise to the mononuclear complexes [Ni(Hotsb)2]Cl2 · H2O (1) and [Cu(Hotsb)Cl2] · H2O (2). These complexes have been characterized by X-ray crystallography, spectroscopy, and cyclic voltammetry. The nickel(II) ion in (1) is in a six-coordinate octahedral environment being bonded to the two protonated tridentate ligands which occupy mer positions. The copper(II) ion in (2) is in a five-coordinate square-pyramidal geometry, in which the basal plane is made up the two nitrogens, sulfur, and chloride atom, while the other chloride atom is coordinated at the axial position. The cyclic voltammogram of the complexes displays two one-electron waves corresponding to MII/MIII and MII/MI processes. The electronic as well as infrared spectral properties of the title complexes are reported and discussed.
机译:三齿配体2-Oximino-3-thiosemicarbazone-2,3-butanedione(Hotsb)与MCl2 (M = Ni2 + 或Cu2 + )反应生成单核络合物[Ni (Hotsb)2 ] Cl2 ·H2 O(1)和[Cu(Hotsb)Cl2 ]·H2 O(2)。这些配合物已通过X射线晶体学,光谱学和循环伏安法进行了表征。 (1)中的镍(II)离子处于六坐标八面体环境中,与两个占据mer位置的质子化三齿配体键合。 (2)中的铜(II)离子呈五坐标方锥几何结构,其中基面由两个氮,硫和氯原子组成,而另一个氯原子在轴向位置被配位。配合物的循环伏安图显示了两个对应于MII / MIII 和MII / MI 过程的单电子波。报告和讨论了标题配合物的电子和红外光谱性质。

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  • 来源
    《Transition Metal Chemistry》 |2008年第1期|99-105|共7页
  • 作者单位

    Department of Chemistry Education Kongju National University Kongju 314-701 Korea;

    Department of Chemistry Education Kongju National University Kongju 314-701 Korea;

    Department of Chemistry Education Kongju National University Kongju 314-701 Korea;

    Department of Chemistry Education Kongju National University Kongju 314-701 Korea;

    Department of Culture Heritage Conservation Science Kongju National University Kongju 314-701 Korea;

    Department of Culture Heritage Conservation Science Kongju National University Kongju 314-701 Korea;

    Department of Geoenvironmental Science Kongju National University Kongju 314-701 Korea;

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