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Extended one- and two-dimensional copper(II) complexes with bridging (N-N) diazine ligands: structural and magnetic studies

机译:具有桥联(N-N)二嗪配体的扩展一维和二维铜(II)配合物:结构和磁性研究

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One- and two-dimensional copper(II) complexes of the polydentate diazine ligands pahap and pypz are reported, in which two copper(II) centers are bridged by a rotationally flexible single N-N bridge in a basic dinuclear subunit, with these subunits linked by halogen atom bridges to provide extended chains and layers. Crystal structures are reported for [Cu-2(pypz)Cl-4]. H2O (1), [Cu-2(pypz)Br-4]. H2O (2) and [Cu-2(pahap)Cl-4] (3). In 1 and 2 the dinuclear subunits are internally bridged by halogen atoms to form tetranuclear dimers, which then link to form a two-dimensional chicken wire lattice. The dinuclear subunits exhibit intra-molecular ferromagnetic coupling, associated with acute angles of rotation of the copper magnetic planes around the N-N single bond bridge, in complete agreement with previous magneto-structural results. However, low temperature phase transitions (< 15 K) indicate the presence of significant antiferromagnetic components, which are associated with spin pairing between adjacent ferromagnetic layers. In addition long range, weak ferromagnetic ordering is observed below 5 K, and confirmed by magnetic hysteresis measurements. The complicated magnetic data have been interpreted in terms of a model involving one-dimensional ferromagnetic chains arranged in two-dimensional layers, with the layers linked antiferromagnetically, leading to metamagnetic behaviour, with additional interchain ferromagnetic coupling appearing at low temperatures. Compound 3 has a much larger rotational angle of the copper magnetic planes around the N-N bond (120.3 degrees), and a different extended structure involving a linear chain of chlorine atom bridged tetranuclear subunits. The magnetic properties of 3 are interpreted using an alternating chain model, and are dominated by intramolecular antiferromagnetic exchange between copper(II) centers within each dinuclear subunit. [References: 41]
机译:报道了多齿二嗪配体pahap和pypz的一维和二维铜(II)配合物,其中两个铜(II)中心通过旋转柔性单NN桥连接在基本双核亚基中,这些亚基通过卤素原子桥可提供延伸的链和层。据报道[Cu-2(pypz)Cl-4]的晶体结构。 H 2 O(1),[Cu-2(pypz)Br-4]。 H 2 O(2)和[Cu-2(pahap)Cl-4](3)。在1和2中,双核亚基在内部被卤素原子桥接形成四核二聚体,然后四核二聚体连接形成二维鸡丝晶格。双核亚基表现出分子内铁磁耦合,与围绕N-N单键桥的铜磁平面的锐角旋转有关,与先前的磁结构结果完全一致。但是,低温相变(<15 K)表示存在大量反铁磁成分,这些成分与相邻铁磁层之间的自旋配对相关。此外,在远距离范围内,在5 K以下观察到弱的铁磁有序性,并通过磁滞测量得到证实。复杂的磁数据已经按照涉及一维铁磁链的模型进行了解释,该一维铁磁链排列在二维层中,各层以反铁磁方式链接,从而导致超磁行为,并且在低温下还会出现链间铁磁耦合。化合物3具有围绕N-N键的铜磁性平面更大的旋转角度(120.3度),并且具有不同的扩展结构,该结构涉及氯原子桥接的四核亚基的线性链。使用交替链模型解释3的磁性,并由每个双核亚基内铜(II)中心之间的分子内反铁磁交换控制。 [参考:41]

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