Kaabi Kamel, El Glaoui Meher, Zeller Matthias, Ben Nasr Cherif
Acta Crystallogr Sect E Struct Rep Online. 2010 Aug 21;66(Pt 9):m1145-6. doi: 10.1107/S160053681003312X.
In the title compound, [Cu(ClO(4))(2)(C(12)H(8)N(2))(H(2)O)(2)], the Cu(II) atom is coordinated in a square-planar fashion by the two N atoms of a chelating 1,10-phenanthroline ligand and by two water mol-ecules trans to the N atoms. The coordination sphere of the metal atom is augmented by O atoms of two weakly bonded perchlorate anions, thus yielding a strongly distorted CuN(2)O(4) octa-hedral environment. The crystal packing is stabilized by O-H⋯O hydrogen bonds between the water mol-ecules and the perchlorate anions. In addition, the organic mol-ecules are associated by π-π stacking inter-actions between symmetry-equivalent anti-parallel non-nitro-gen aromatic rings, with inter-planar distances of 3.543 (2) Å.
在标题化合物[Cu(ClO₄)₂(C₁₂H₈N₂)(H₂O)₂]中,Cu(II)原子通过螯合的1,10 - 菲咯啉配体的两个N原子以及与N原子相对的两个水分子以平面正方形方式配位。金属原子的配位球通过两个弱键合的高氯酸根阴离子的O原子得以扩展,从而形成一个严重扭曲的CuN₂O₄八面体环境。晶体堆积通过水分子与高氯酸根阴离子之间的O—H⋯O氢键得以稳定。此外,有机分子通过对称等效的反平行非氮芳香环之间的π - π堆积相互作用缔合,平面间距离为3.543(2) Å。