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配合物[Zn(BCBI)_2(H_2O)_4]·2H_2O的合成及其晶体结构 被引量:1

Synthesis and Crystal Structure of Complex [Zn(BCBI)_2(H_2O)_4]·2H_2O
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摘要 以ZnCl2,1,3-二羧甲基苯并咪唑为原料,采用常温溶剂挥发法,在甲醇水溶液中合成了Zn(Ⅱ)配合物{[Zn(BCBI)2(H2O)4].2H2O(1)},其结构经IR,元素分析和X-射线单晶衍射表征。1属三斜晶系,P-1空间群,晶胞参数a=7.4009(15),b=9.4066(19),c=9.6559(19),α=81.58(3)°,β=75.97(3)°,γ=78.08(3)°,V=634.8(2)3,Z=1,Dc=1.674 mg.cm-3,μ=1.050 mm-1,S=1.023。1中Zn(Ⅱ)与六个氧原子配位(两个氧原子来自两个配体H2BCBI分子中的羧基氧,四个氧原子为四个H2O的氧原子)形成变形的八面体构型。1的分子间氢键及H2BCBI间的π-π堆积将其拓展为三维结构,并对稳定晶体结构起着重要作用。 Complex [Zn(BCBI)2(H2O)4]·2H2O(1) was synthesized by reaction of 1,3-bis-carboxymethyl-benzimidazole(H2BCBI) with zinc chloride in an aqueous solution of methanol by solvent evaporation method.The structure was characterized by IR,elemental analysis and X-ray single crystal diffraction.1 belongs to triclinic system,space group P-1 with a=7.400 9(15),b=9.4066(19),c=9.6559(19),α=81.58(3)°,β=75.97(3)°,γ=78.08(3)°,V=634.8(2)3,Z=1,Dc=1.674 mg·cm-3,μ=1.050 mm-1,S=1.023.Zn(Ⅱ) in 1 is coordinated with four water molecules and two monodentate H2BCBI ligands in a slightly distorted octahedral geometry.The crystal structure is stabilized by intermolecular O-H┈O hydrogen bonds and the aromatic weak π-π packing interactions,which extended 1 into a three-dimensional open framework,which is important for stabilizing the structure.
出处 《合成化学》 CAS CSCD 北大核心 2011年第1期69-72,共4页 Chinese Journal of Synthetic Chemistry
基金 新疆大学博士启动基金资助项目(BS07020428022)
关键词 1 3-二羧甲基苯并咪唑 Zn(Ⅱ) 配合物 合成 晶体结构 1 3-bis-carboxymethyl-benzimidazole Zn(Ⅱ) complex synthesis crystal structure
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