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首页> 外文期刊>European journal of inorganic chemistry >mu-1,3-(trans) and mu-1,2-(cis) bonding in squarato-bridged dinuclear copper(II) and nickel(II) complexes derived from polypyridyl amines
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mu-1,3-(trans) and mu-1,2-(cis) bonding in squarato-bridged dinuclear copper(II) and nickel(II) complexes derived from polypyridyl amines

机译:由聚吡啶胺衍生的方桥双核铜(II)和镍(II)络合物中的mu-1,3-(反式)和mu-1,2-(顺式)键

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摘要

A novel series of dinuclear squarato-bridged copper(II) and nickel(II) complexes [Cu-2(TPA)(2)(mu(1,3)-C4O4)](ClO4)(2)center dot 4H(2)O (1), [Cu-2(MeDPA)(2)(mu(1,3)-C4O4)(H2O)(4)](ClO4)(2) (2) and [Ni-2(TPA)(2)-(mu(1,2)-C4O4)(H2O)(2)](ClO4)(2) (3) [C4O42- = dianion of 3,4-dihydroxycyclobut-3-en-1,2-dione (squaric acid), MeDPA = N-methylbis(2-pyridylmethyl)amine, TPA = tris(2-pyridylmethyl)amine] were synthesized and Structurally characterized by X-ray crystallography. Them spectral and structural characterizations as well as their magnetic Properties are reported. In this series, the structures consist of the ClO4- groups as counterions and the C4O42- anions bridging the two M-II centers in a mu-1,3-(1 and 2) or in a mu-1,2-bis(monodentate) (3) bonding fashion. The coordination geometry around the five-coordinate Cu-II centers in 1 is a distorted trigonal bipyramid, where the coordination environment is achieved by the four N-donor atoms of the TPA ligand and one oxygen atom of the bridging squarato ligand. The complexes 2 and 3 adopt a distorted octahedral geometry. The six-coordinate 4+2 environment in 2 is achieved by the three N-atoms of the MeDPA ligand, by an oxygen atom of a bridging squarato ligand and, at longest distances, by two oxygen atoms from coordinated water molecules. In the nickel complex 3, the geometry is attained by the four N-atoms of TPA and by two oxygen atoms supplied by a coordinated water molecule and by a bridging squarato ligand. The results manifested the effects of the blocking amine variations on the structure and on the bonding mode of the bridging squarato ligand, The complexes show antiferromagnetic coupling with vertical bar J vertical bar = 9.1 and 1.2 cm(-1) in the mu-1,3-bridged squarato compounds 1 and 2, and with J = -1.4 cm(-1) in the corresponding mu-1,2-bridged squarato complex 3. The magnetic properties are discussed in relation to other related compounds and the structural data. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008).
机译:新型的双核方形桥联铜(II)和镍(II)络合物[Cu-2(TPA)(2)(mu(1,3)-C4O4)(ClO4)(2)中心点4H(2 )O(1),[Cu-2(MeDPA)(2)(mu(1,3)-C4O4)(H2O)(4)](ClO4)(2)(2)和[Ni-2(TPA) (2)-(mu(1,2)-C4O4)(H2O)(2)](ClO4)(2)(3)[C4O42- = 3,4-二羟基环丁-3-en-1,2-的二价阴离子合成二酮(方酸),MeDPA = N-甲基双(2-吡啶基甲基)胺,TPA =三(2-吡啶基甲基)胺],并通过X射线晶体学对其结构进行表征。报告了它们的光谱和结构特征以及它们的磁性能。在这个系列中,结构由作为抗衡离子的ClO4-基和桥接在mu-1,3-(1和2)或mu-1,2-bis(两个)中的两个M-II中心的C4O42-阴离子组成。单齿)(3)粘接方式。 1的5个坐标的Cu-II中心周围的配位几何结构是扭曲的三角双锥,其中通过TPA配体的四个N供体原子和桥连的方形配体的一个氧原子实现了配位环境。配合物2和3采用扭曲的八面体几何形状。通过MeDPA配体的三个N原子,桥连的方形配体的一个氧原子,以及在最长距离处,从配位的水分子中获得两个氧原子,可以实现2中六配位的4 + 2环境。在镍配合物3中,通过TPA的四个N原子以及通过配位水分子和桥连的方配体提供的两个氧原子获得几何形状。结果表明,封端胺的变化对架桥方配体的结构和键合模式的影响。配合物在mu-1中显示出反铁磁耦合,其中竖线J竖线= 9.1和1.2 cm(-1), 3桥联的方化合物1和2,以及在相应的mu-1,2-桥联的方合物3中J = -1.4 cm(-1)。讨论了与其他相关化合物和结构数据有关的磁性能。 ((C)Wiley-VCH Verlag GmbH&Co.KGaA,69451 Weinheim,Germany,2008)。

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