Yin Hua
Instrumental Measurement and Analysis Centre, Fuzhou University, Fuzhou, Fujian 350002, People's Republic of China.
Acta Crystallogr C. 2008 Oct;64(Pt 10):m324-6. doi: 10.1107/S0108270108026401. Epub 2008 Sep 20.
In the title centrosymmetric binuclear complex, Cu(2)(C(14)H(11)N(2)O(3))(2)(H(2)O)(2)(2), the two metal centres are bridged by the phenolate O atoms of the ligand, forming a Cu(2)O(2) quadrangle. Each Cu atom has a distorted square-pyramidal geometry, with the basal donor atoms coming from the O,N,O'-tridentate ligand and a symmetry-related phenolate O atom. The more weakly bound apical donor O atom is supplied by a coordinated water molecule. When a further weak Cu...O interaction with the 4-hydroxy O atom of a neighbouring cation is considered, the extended coordination sphere of the Cu atom can be described as distorted octahedral. This interaction leads to two-dimensional layers, which extend parallel to the (100) direction. The two-dimensional polymeric structure contrasts with other reported structures involving salicylaldehyde benzoylhydrazone ligands, which are usually discrete mono- or dinuclear Cu complexes. The nitrate anions are involved in a three-dimensional hydrogen-bonding network, featuring intermolecular N-H...O and O-H...O hydrogen bonds.
在标题为中心对称双核配合物Cu₂(C₁₄H₁₁N₂O₃)₂(H₂O)₂₂中,两个金属中心由配体的酚氧原子桥连,形成一个Cu₂O₂四边形。每个铜原子具有扭曲的四方锥几何构型,其底面供体原子来自O,N,O'-三齿配体和一个对称相关的酚氧原子。较弱配位的顶端供体氧原子由一个配位水分子提供。当考虑与相邻阳离子的4-羟基氧原子的进一步弱Cu...O相互作用时,铜原子的扩展配位球可描述为扭曲的八面体。这种相互作用导致二维层,其平行于(100)方向延伸。这种二维聚合物结构与其他报道的涉及水杨醛苯甲酰腙配体的结构形成对比,后者通常是离散的单核或双核铜配合物。硝酸根阴离子参与三维氢键网络,其特征为分子间N-H...O和O-H...O氢键。