Ag(Ⅰ) Schiff碱配合物的合成及其晶体结构
Synthesis and Crystal Structure of Ag(Ⅰ) Schiff Base Complex
作者单位
张奇龙 贵阳医学院化学教研室贵阳 550004 
张云黔 贵州省大环化学及超分子化学重点实验室贵阳 550025 
朱必学 贵州省大环化学及超分子化学重点实验室贵阳 550025 
摘要: 本文以2-醛基吡啶和1,2-二(对氨基苯氧基)乙烷进行缩合得到Schiff碱配体L,再分别同AgNO3和AgClO4进行配位反应,得到了2个配合物[Ag2(NO3)2L] (1)和{[AgL]ClO4}n (2),并用元素分析,FTIR和X-射线单晶衍射进行了表征。结果表明,配合物1属于单斜晶系,P21/c空间群,Ag(I)的配位环境为平面三角形,配体L同时和2个Ag(Ⅰ)离子配位形成双核配合物。配合物2属于单斜晶系,P21/n空间群,每个Ag(Ⅰ)的配位环境均为扭曲四面体,每个配体L通过其两端的2个氮原子同2个金属离子配位桥联形成一维螺旋链结构。
关键词: 席夫碱  Ag(Ⅰ)配合物  晶体结构
基金项目: 
Abstract: The Schiff base ligand L was synthesized from condensation reaction of 1,2-( p-aminophenoxy)ethane with 2-Pyridinecarboxaldehyde. AgNO3 and AgClO4 each react with L to give two complexes [Ag2(NO3)2L] (1) and {[AgL]ClO4}n (2), and characterized by elemental analysis, FTIR and single crystal X-ray diffraction. The results of structural analysis indicate that the complex 1 is monoclinic crystallize and space group P21/c, the coordination environment of Ag(Ⅰ) is a plane triangular, each L ligand links two metal atoms form a binuclear complex. The complex 2 is monoclinic crystallize and space group P21/n, the coordination environment of Ag(Ⅰ) is a distorted tetrahedron, each L ligand links two metal atoms using both ends two nitrogen atom to generate a one-dimensional (1D) helical chain structure. CCDC: 815860, 1; 815861, 2.
Keywords: Schiff base  Ag(Ⅰ) complex  crystal structure
 
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张奇龙,张云黔,朱必学.Ag(Ⅰ) Schiff碱配合物的合成及其晶体结构[J].无机化学学报,2011,27(11):2191-2194.
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