首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Supramolecular networks of Mn(III)-Schiff base complexes assembled by nitrate counterions: X-ray crystal structures of 1D chains and 2D networks
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Supramolecular networks of Mn(III)-Schiff base complexes assembled by nitrate counterions: X-ray crystal structures of 1D chains and 2D networks

机译:硝酸盐抗衡离子组装的Mn(III)-席夫碱配合物的超分子网络:一维链和二维网络的X射线晶体结构

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A series of Mn(III) nitrate complexes have been synthesized from dianionic hexadentate Schiff bases obtained by condensation of 3-methoxy-2- hydroxybenzaldehyde with different diamines. The complexes have been characterised by elemental analysis, ESI mass spectrometry, IR and ~1H NMR spectroscopy. Magnetic studies and molar conductivity measurements were also performed. Complexes [MnL~1(H_2O)_2]_2·2NO_3·2CH_3OH (1), [MnL ~2(H_2O)_2]_2·2NO _3·2CH_3OH (2) and [MnL~5(H_2O)_2]_2·2NO_3·6H_2O (5) were crystallographically characterised. The X-ray structures show an octahedral geometry around the metal with the Schiff base in the equatorial plane acting as tetradentate and water or methanol molecules in the axial positions. The octahedron entities are linked in pairs by μ-aquo bridges between neighbouring axial water molecules and also by π-π stacking interactions, establishing dimeric and polymeric structures. Nitrate anions are accommodated in the cavities of the framework and form hydrogen bonds with the aqua ligands and the methanol or crystal water, leading to infinite supramolecular aggregates of the complexes. Comparison of chloride, perchlorate and nitrate complexes indicate that the nature of the anions is the key factor directing the structural topologies.
机译:从3-甲氧基-2-羟基苯甲醛与不同的二胺缩合得到的双阴离子六齿席夫碱合成了一系列硝酸锰(III)配合物。通过元素分析,ESI质谱,IR和〜1H NMR光谱对复合物进行了表征。还进行了磁研究和摩尔电导率测量。配合物[MnL〜1(H_2O)_2] _2·2NO_3·2CH_3OH(1),[MnL〜2(H_2O)_2] _2·2NO _3·2CH_3OH(2)和[MnL〜5(H_2O)_2] _2·2NO_3 ·6H_2O(5)的晶体学表征。 X射线结构显示出金属周围的八面体几何形状,赤道面上的席夫碱作为四齿,轴向上的水或甲醇分子起作用。八面体实体通过相邻轴向水分子之间的a-aquo桥成对连接,也通过π-π堆积相互作用成对连接,从而建立了二聚体和聚合物结构。硝酸根阴离子被容纳在骨架的空腔中,并与水配体和甲醇或结晶水形成氢键,导致络合物的无限超分子聚集。氯离子,高氯酸根和硝酸根络合物的比较表明,阴离子的性质是指导结构拓扑的关键因素。

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