原位水热合成一个新颖的银四唑配位聚合物(英)
Indirectly In-Situ Hydrothermal Preparation of a Novel Ag Tetrazole Coordination Polymer
作者单位
王锡森 南京大学配位化学研究所配位化学国家重点实验室南京 210093 
唐云志 南京大学配位化学研究所配位化学国家重点实验室南京 210093 
熊仁根 南京大学配位化学研究所配位化学国家重点实验室南京 210093 
摘要: 在水热条件下,硝酸(3-氰基吡啶)银以及叠氮化纳反应,成功地组装了一个二维层状银四唑配位聚合物[mono(5-(3-pyridyl)tetrazolato)Ag] (1),并对其进行了表征。晶体结构分析表明,化合物1结晶在三斜晶系,其空间群分别为P1(a=0.626 08(10) nm,b=0.784 98(13) nm,c=0.805 84(12) nm,α=75.171(4)°,β=76.653(3)°,γ=68.332(3)°,V=0.351 67(10) nm3Z=2),银的配位环境为四配位并形成略为变形的四面体构型。室温下,化合物1显示强的蓝色荧光(495 nm和521 nm)。
关键词:   原位  四唑配位聚合物  水热合成  荧光
基金项目: 
Abstract: The reaction of Ag(3-cyanopyridine)NO3 with NaN3 in presence of water and ethanol affords an unprecedented 2D layered tetrazole coordination polymer, [mono(5-(3-pyridyl) tetrazolato)Ag], [(3-PTZ)Ag] (1), which is characterized by single crystal X-ray determination, IR and fluorescent spectrum. The local coordination geometry around the Ag ion can be best described as a slightly distorted tetrahedron. The fluorescent emission spectrum of 1 at the solid-state at room temperature shows that maximal emission peak occurs in 495 and 521 nm, respectively. Crystal data for 1, C6H4AgN5, triclinic, P1, a=0.626 08(10) nm, b=0.784 98(13) nm, c=0.805 84(12) nm, α=75.171(4)°, β=76.653(3)°, γ=68.332(3)°, V=0.351 67(10) nm3, Z=2. CCDC: 267340.
Keywords: Ag  in situ  tetrazole coordination polymer  hydrothermal synthesis  fluorescence
投稿时间:2005-04-01 修订日期:2005-05-31
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王锡森,唐云志,熊仁根.原位水热合成一个新颖的银四唑配位聚合物(英)[J].无机化学学报,2005,21(7):1025-1029.
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