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首页> 外文期刊>Acta Crystallographica Section E: Crystallographic Communications >Di-μ-hydroxido-bis-[hemiaqua-(N,N,N′,N′-tetra-methyl-ethane-1,2-diamine)-copper(II)] bis-(tetra-fluoridoborate)
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Di-μ-hydroxido-bis-[hemiaqua-(N,N,N′,N′-tetra-methyl-ethane-1,2-diamine)-copper(II)] bis-(tetra-fluoridoborate)

机译:二μ-羟基双(四氟(N,N,N',N'-四甲基乙烷-1,2-二胺)-铜(II)]双(四氟硼酸酯)

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摘要

The title compound, [Cu2(OH)2(C6H16N2)2(H2O)](BF4)2, consists of dinuclear centrosymmetric [Cu2(OH)2(tmen)2(H2O)]2+ complex cations (tmen = N,N,N′,N′-tetra-methyl-ethane-1,2-diamine) and tetra-fluoridoborate anions. In the cation, the CuII atom shows a slightly distorted square-pyramidal coordination geometry provided by a pair of μ-OH? anions and by the N atoms of a chelate tmen ligand in the basal plane. The apical position is statistically occupied by the O atom of a half-occupancy water mol-ecule. The F atoms of the anion are disordered over three sets of sites with occupancies of 0.598?(9):0.269?(6):0.134?(8). The crystal packing is governed by ionic forces as well as by O—H?F hydrogen bonds.
机译:标题化合物[Cu2(OH)2(C6H16N2)2(H2O)](BF4)2由双核中心对称的[Cu2(OH)2(tmen)2(H2O)] 2+复合阳离子(tmen = N, N,N',N'-四甲基乙烷-1,2-二胺)和四氟硼酸根阴离子。在阳离子中,CuII原子显示出由一对μ-OH2提供的略微扭曲的方金字塔配位几何形状。阴离子和基面螯合tmen配体的N原子。从统计学上讲,顶端位置被一个半占位水分子的O原子占据。阴离子的F原子在三组位点上无序,占有率为0.598?(9):0.269?(6):0.134?(8)。晶体堆积受离子力以及OH F氢键的控制。

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