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Syntheses, structures and magnetic properties of three-dimensional co-ordination polymers constructed by dimer subunits

机译:二聚体亚单元构建的三维配位聚合物的合成,结构和磁性

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摘要

The crystal structures and magnetic properties of compounds [M~(II)(apo)(N(CN)_2)_2], where M = Co (1), Ni (2) or Mn (3), apo = 2-aminopyridine N-oxide, have been determined. The structural analysesrevealed that they are isomorphous, and all belong to monoclinic space group P2_1. The metal(II) ions display distorted octahedral co-ordination, with four terminal N atoms of different [N(CN)_2]~- ligands and two O atoms of different apo ligands. Two ions are bridged by two #mu#-O atoms to form a dimer subunit. Those dimers are further linked to each other by [N(CN)_2]~- resulting in a three-dimensional structure. The magnetic properties of the compounds were nvestigated in the temperature range 2-300 K for 1 and 2 and 4-300 K for 3. The values for the intradimer spin coupling constant J were estimated to be -17.8, -40, -1.3, respectively, indicative of antiferromagnetic interaction.
机译:化合物[M〜(II)(apo)(N(CN)_2)_2]的晶体结构和磁性能,其中M = Co(1),Ni(2)或Mn(3),apo = 2-氨基吡啶已确定N-氧化物。结构分析表明它们是同构的,都属于单斜空间群P2_1 / n。金属(II)离子显示扭曲的八面体配位,具有不同[N(CN)_2]〜-配体的四个末端N原子和不同载脂蛋白配体的两个O原子。两个离子被两个#mu#-O原子桥接形成二聚体亚基。这些二聚体进一步通过[N(CN)_2]-彼此连接,从而形成三维结构。在1和2的2-300 K温度范围和3的4-300 K温度范围内研究了化合物的磁性。二聚体内自旋偶合常数J的值估计为-17.8,-40,-1.3,分别表示反铁磁相互作用。

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