Sertçelik Mustafa, Caylak Delibaş Nagihan, Necefoğlu Hacali, Hökelek Tuncer
Acta Crystallogr Sect E Struct Rep Online. 2012 Jul 1;68(Pt 7):m946-7. doi: 10.1107/S1600536812026943. Epub 2012 Jun 20.
In the title complex, [Ni(C(8)H(5)O(3))(2)(C(6)H(6)N(2)O)(2)(H(2)O)(2)], the Ni(II) cation is located on an inversion center and is coordinated by two 4-formyl-benzoate (FB) anions, two nicotinamide (NA) ligands and two water mol-ecules. The four O atoms in the equatorial plane around the Ni(II) cation form a slightly distorted square-planar arrangement, while the slightly distorted octa-hedral coordination is completed by the two N atoms of the NA ligands in the axial positions. The dihedral angle between the carboxyl-ate group and the adjacent benzene ring is 23.67 (8)°, while the pyridine and benzene rings are oriented at an angle of 89.04 (4)°. The coordinating water mol-ecule links with the carboxyl-ate group via an O-H⋯O hydrogen bond. In the crystal, N-H⋯O, O-H⋯O and weak C-H⋯O hydrogen bonds link the mol-ecules into a three-dimensional supra-molecular network. π-π contacts between benzene rings [centroid-centroid distance = 3.8414 (7) Å] may further stabilize the structure. A weak C-H⋯π inter-action also occurs.
在标题配合物[Ni(C₈H₅O₃)₂(C₆H₆N₂O)₂(H₂O)₂]中,Ni(II)阳离子位于一个对称中心上,由两个4-甲酰基苯甲酸根(FB)阴离子、两个烟酰胺(NA)配体和两个水分子配位。Ni(II)阳离子周围赤道平面上的四个O原子形成略微扭曲的平面正方形排列,而轴向位置上NA配体的两个N原子则完成了略微扭曲的八面体配位。羧酸根基团与相邻苯环之间的二面角为23.67 (8)°,而吡啶环和苯环的取向角度为89.04 (4)°。配位水分子通过O—H⋯O氢键与羧酸根基团相连。在晶体中,N—H⋯O、O—H⋯O和弱C—H⋯O氢键将分子连接成三维超分子网络。苯环之间的π-π接触[质心-质心距离 = 3.8414 (7) Å]可能进一步稳定结构。还存在弱C—H⋯π相互作用。