Syntheses,Structural Characterization and Fluorescent Properties of Zn(Ⅱ),Cd(Ⅱ) and (E)-N1-(pyridin-4-ylmethylene) benzene-1,4-diamine Sulphate Complex Salts
采用相同条件的液相层置法将Zn2+、Cd2+;的硫酸盐与配体N-(1-亚甲基-4-吡啶基)-1,4-苯二胺((E)-N1-(pyridin-4-ylmethyl; ene)benzene-1,4-diamine,pbda))反应,形成配合物[Zn2(;pbda)2(H2O)8] ·; 2SO4(1),[;Cd(pbda)2(;H2O)2(SO4);]nH1:β=β0+α;n,通过红外光谱、X射线单晶衍射对其组成和结构进行了表征,然后测试了单体和配合物的荧光性质.晶体结构的分析结果表明:配合物的结构由金属离子; 的半径调控;尽管Cd2+的离子半径显著大于Zn2+;,但其合成的配合物的中心金属离子的配位数均为6,而配位方式和结构却完全不同;半径较大的金属离子更倾向于形成较高维数的结构;两者结构的不同导; 致其荧光性质存在着显著的差异.Two complexes,[Zn2(pbda)2; (H2O)8] · 2SO4; (1) and [Cd(;pbda)2(H2O;)2(SO4)]n(;2) (pbda = (E)-N1-(pyridin-4-ylmethylene); benzene-1,4-diamine) were synthesized using layer diffusion under the; same condition. The complexes were characterized using IR spectra and; X-ray single crystal diffraction and showed completely different; fluorescent properties. Crystal structure analysis reveals that the; structures of the complexes are controlled by the radii of the metal; ions. Although Cd2+ ion is significantly larger; than Zn2+ ion, both of the coordination numbers; of metal centers in these complexes are 6,and the coordination modes and; structures are completely different. The metal ion with larger radius; tends to form higher dimensional structure. Different coordinated; structures lead to different fluorescent emissions.国家自然科学基金; 国家基础科学人才培养基