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Ag(Ⅰ)Schiff碱配合物的合成及其晶体结构 被引量:4

Synthesis and Crystal Structure of Ag(Ⅰ) Schiff Base Complex
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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。 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 {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.
出处 《无机化学学报》 SCIE CAS CSCD 北大核心 2011年第11期2191-2194,共4页 Chinese Journal of Inorganic Chemistry
基金 贵州省国际合作重点项目(No.黔科合外G字[2009]700104)资助
关键词 席夫碱 Ag(Ⅰ)配合物 晶体结构 Schiff base Ag(Ⅰ) complex crystal structure
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