Moroz Olesia V, Trush Viktor A, Sliva Tatiana Yu, Konovalova Irina S, Amirkhanov Vladimir M
Taras Shevchenko National University of Kyiv, Department of Chemistry, 64/13 Volodymyrska Street, Kyiv 01601, Ukraine.
STC "Institute for Single Crystals", National Academy of Science of Ukraine, 60 Lenina Avenue, Kharkiv 61001, Ukraine.
Acta Crystallogr Sect E Struct Rep Online. 2014 Oct 8;70(Pt 11):305-8. doi: 10.1107/S160053681402159X. eCollection 2014 Nov 1.
In the molecular structure of the title compound, [NaNi(C18H18N2O4)(NO3)(CH3OH)], the Ni(2+) ion has a slightly distorted square-planar coordination environment defined by two N and two O atoms which belong to a Schiff base ligand, viz. 6,6'-dimeth-oxy-2,2'-[ethane-1,2-diylbis(nitrilo-methanylyl-idene)]diphenolate. Seven O atoms form the coordination environment of the Na(+) ion: four from the Schiff base ligand, two from a bidentate chelating nitrate anion and one O atom from a coordinating methanol mol-ecule. In the crystal, the bimetallic complexes are assembled into chains along the b-axis direction via weak C-H⋯O hydrogen-bond inter-actions. Neighbouring chains are in turn connected through bifurcated O-H⋯O hydrogen bonds that involve the coordinating methanol mol-ecules and the nitrate anions, and through π-π stacking inter-actions between phenyl rings of neighbouring mol-ecules.
在标题化合物[NaNi(C₁₈H₁₈N₂O₄)(NO₃)(CH₃OH)]的分子结构中,Ni(Ⅱ)离子具有由两个N原子和两个O原子定义的略微扭曲的平面正方形配位环境,这两个N原子和两个O原子属于一个席夫碱配体,即6,6'-二甲氧基-2,2'-[乙烷-1,2-二基双(亚氨基甲叉基)]二酚盐。七个O原子形成Na(Ⅰ)离子的配位环境:四个来自席夫碱配体,两个来自双齿螯合硝酸根阴离子,一个O原子来自配位甲醇分子。在晶体中,双金属配合物通过弱的C-H⋯O氢键相互作用沿b轴方向组装成链。相邻的链又通过涉及配位甲醇分子和硝酸根阴离子的分叉O-H⋯O氢键以及相邻分子苯环之间的π-π堆积相互作用相连。