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柔性多羧酸配体锶配合物的合成、晶体结构及拓扑学分析
引用本文:王 彦,汪快兵,陈友存,刘光祥.柔性多羧酸配体锶配合物的合成、晶体结构及拓扑学分析[J].无机化学学报,2011,27(11):2303-2307.
作者姓名:王 彦  汪快兵  陈友存  刘光祥
作者单位:1. 安庆师范学院化学化工学院-安徽省功能配合物重点实验室,安庆246011;南京大学配位化学国家重点实验室,南京210093
2. 安庆师范学院化学化工学院-安徽省功能配合物重点实验室,安庆,246011
摘    要:利用水热合成制备了一个新颖的基于柔性多羧酸配体的碱土金属配合物Sr(BuTA)0.5(H2O)2(1)(H4BuTA=1,2,3,4-丁四酸)。利用元素分析及X-射线单晶衍射对其进行了表征。结构分析结果表明标题化合物1属于单斜晶系,P21/c空间群,晶胞参数为a=0.870 03(5) nm,b=0.793 03(5) nm,c=1.268 07(5) nm,β=127.689(3)°,晶胞体积V=0.692 36(7) nm3,Z=4,Dcalc=2.290 g·cm-3F(000)=468,μ=7.768 cm-1R=0.015 8,wR=0.037 7。在化合物1中,每个Sr(Ⅱ)的配位环境为八配位的反四棱柱配位构型。在配合物中金属和配体互相连接形成一个三维的框架结构,其拓扑为(46)2(412.612.84)。在其结构中配体是少见的八连接点。对配合物1的热稳定性也做了测试。

关 键 词:晶体结构    锶配合物    拓扑    羧酸配体

Syntheses, Characterization, and Topological Analysis of an Alkaline Earth Metal-Organic Frameworks with Flexible Multi-Carboxylic ligand
WANG Yan,WANG Kuai-Bing,CHEN You-Cun and LIU Guang-Xiang.Syntheses, Characterization, and Topological Analysis of an Alkaline Earth Metal-Organic Frameworks with Flexible Multi-Carboxylic ligand[J].Chinese Journal of Inorganic Chemistry,2011,27(11):2303-2307.
Authors:WANG Yan  WANG Kuai-Bing  CHEN You-Cun and LIU Guang-Xiang
Institution:School of Chemistry and Chemical Engineering, Anhui Key Laboratory of Functional Coordination Compounds, Anqing Teachers College, Anqing, Anhui 246011, China; State Key Laboratory of Coordination Chemistry, Nanjing University, Nanjing 210093, China,School of Chemistry and Chemical Engineering, Anhui Key Laboratory of Functional Coordination Compounds, Anqing Teachers College, Anqing, Anhui 246011, China,School of Chemistry and Chemical Engineering, Anhui Key Laboratory of Functional Coordination Compounds, Anqing Teachers College, Anqing, Anhui 246011, China and School of Chemistry and Chemical Engineering, Anhui Key Laboratory of Functional Coordination Compounds, Anqing Teachers College, Anqing, Anhui 246011, China
Abstract:A alkaline earth metal-organic complex,namely,Sr(BuTA)0.5(H2O)2 (1) (H4BuTA=1,2,3,4-Butanetetra-carboxylic acid),was obtained in water system by hydrothermal method based on flexible multi-carboxylate ligand.The title complex was characterized by elemental analysis and X-ray crystallography.The result of structural analysis shows that the complex 1 crystallizes in monoclinic,space group P21/c with a=0.870 03(5) nm,b=0.793 03(5) nm,c=1.268 07(5) nm,β=127.689(3)°,V=0.692 36(7) nm3,g=4,Dc=2.290 g·cm-3,F(000)=468,μ=7.768 cm-1,the final R =0.015 8,wR =0.037 7.In complex 1,the coordination environment of Sr(Ⅱ) is eightcoordinated with square antiprismatic geometry.The metal ions and ligands link each other to form a 3D framework of (46)2(412.612.84) topology,in which the BuTA2- anions act as rare 8-connected topological blocks.The thermal stability of complex 1 was also investigated.CCDC:825571.
Keywords:crystal structure  Sr(Ⅱ) complex  topochemistry  carboxylate ligand
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