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Crystal structures and magnetic properties of nitroxide radical-coordinated copper(II) and cobalt(II) complexes

机译:氮氧化物自由基配位铜(II)和钴(II)配合物的晶体结构和磁性结构

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摘要

The crystal structures and magnetic properties of three coordination compounds constructed from various nitroxide radicals L and M-II(hfac)(2)(H2O)(2) building blocks (M=Cu or Co and hfac=hexafluoroacetylacetonato) are described. In [(1)Cu(hfac)(2)](n), 4, the radical ligand L is coordinated to the metal through the oxygen atom of the nitroxide group and oxygen atom of its hydroxyl group, leading to a one-dimensional chain system. In [(2)(2)Cu(hfac)(2)](n), 5, two hydroxyl oxygen atoms of the radical ligand are coordinated to the metal, and the Co-II centers adopt distorted octahedral geometry to give a mononuclear compound. For [(L)Cu(hfac)(2)](n), 6, the oxygen atom of the nitroxide group and nitrogen atom of the amino group of L are coordinated to the metal, leading to a one-dimensional chain system. The magnetic susceptibility study of the copper coordination compound 4 revealed weak ferromagnetic interactions between the metal center and the organic radical. The cobalt coordination compounds 5 and 6 both show antiferromagnetic interactions.
机译:描述了由各种硝基氧化物基团L和M-II(HFAC)(2)(2)(H2O)(2)构建块(M = Cu或Co和HFAC =六氟乙酰丙酮)构成的三种配位化合物的晶体结构和磁性。在[(1)Cu(HFAC)(2)](n),4中,通过硝基氧化物基团的氧原子和其羟基的氧原子配位,使自由基配体L与其羟基的氧原子配合,导致一维链系统。在[(2)(2)Cu(HFAC)(2)](N)中,5,5,基团配体的两个羟基氧原子与金属配位,二十同子中心采用扭曲的八面体几何形状得到单核化合物。对于[(L)Cu(HFAC)(2)](N),6,L的氨基的氧原子和L的氨基的氮原子与金属配位,导致一维链系统。铜配位化合物4的磁化性研究揭示了金属中心与有机基团之间的弱铁磁相互作用。钴配位化合物5和6都显示出反铁磁相互作用。

著录项

  • 来源
    《Transition Metal Chemistry》 |2019年第3期|共10页
  • 作者

    Gao Yan-Li; Inoue Katsuya;

  • 作者单位

    Yulin Univ Sch Chem &

    Chem Engn Yulin 719000 Peoples R China;

    Hiroshima Univ Dept Chem 1-3-1 Kagamiyama Higashihiroshima Hiroshima 7398526 Japan;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 无机化学;
  • 关键词

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