Ibragimov Aziz B
Institute of General and Inorganic Chemistry of Uzbekistan Academy of Sciences, M.Ulugbek Str, 77a, Tashkent 100170, Uzbekistan.
Acta Crystallogr E Crystallogr Commun. 2016 Apr 8;72(Pt 5):643-7. doi: 10.1107/S2056989016005521. eCollection 2016 May 1.
The reaction of 3-hy-droxy-benzoic (m-hy-droxy-benzoic) acid (MHBA), tri-ethano-lamine (TEA) and Ni(NO3)2 in aqueous solution led to formation of the hydrated title salt, Ni(C6H15NO3)2·4H2O. In the complex cation, the Ni(2+) ion is located on an inversion centre. Two symmetry-related TEA ligands occupy all coordination sites in an N,O,O'-tridentate coordination, leading to a slightly distorted NiN2O4 octa-hedron. Two ethanol groups of each TEA ligand form two five-membered chelate rings around Ni(2+), while the third ethanol group does not coordinate to the metal atom. Two MHBA(-) anions in the benzoate form are situated in the outer coordination sphere for charge compensation. An intricate network of hydrogen bonds between the free and coordinating hy-droxy groups of the TEA ligands, the O atoms of the MHBA(-) anions and the water mol-ecules leads to the formation of a two-dimensional structure extending parallel to (010).
3-羟基苯甲酸(间羟基苯甲酸,MHBA)、三乙醇胺(TEA)与硝酸镍在水溶液中反应生成水合标题盐Ni(C6H15NO3)2·4H2O。在配合物阳离子中,Ni(2+)离子位于对称中心。两个对称相关的TEA配体以N,O,O'-三齿配位占据所有配位位点,形成略微扭曲的NiN2O4八面体。每个TEA配体的两个乙醇基团围绕Ni(2+)形成两个五元螯合环,而第三个乙醇基团不与金属原子配位。两个苯甲酸根形式的MHBA(-)阴离子位于外配位层进行电荷补偿。TEA配体的游离羟基和配位羟基、MHBA(-)阴离子的O原子与水分子之间形成复杂的氢键网络,导致形成平行于(010)延伸的二维结构。