侯银玲, 季甲, 周仁迪, 唐光念, 陈宇宇. 新颖一维链Zn配合物的合成、结构及荧光性质[J]. 云南大学学报(自然科学版), 2017, 39(6): 1035-1039. doi: 10.7540/j.ynu.20170161
引用本文: 侯银玲, 季甲, 周仁迪, 唐光念, 陈宇宇. 新颖一维链Zn配合物的合成、结构及荧光性质[J]. 云南大学学报(自然科学版), 2017, 39(6): 1035-1039. doi: 10.7540/j.ynu.20170161
HOU Yin-ling, JI Jia, ZHOU Ren-di, TANG Guang-nian, CHEN Yu-yu. Synthesis,structure and fluorescence of a novel 1D chain Zn coordination compound[J]. Journal of Yunnan University: Natural Sciences Edition, 2017, 39(6): 1035-1039. DOI: 10.7540/j.ynu.20170161
Citation: HOU Yin-ling, JI Jia, ZHOU Ren-di, TANG Guang-nian, CHEN Yu-yu. Synthesis,structure and fluorescence of a novel 1D chain Zn coordination compound[J]. Journal of Yunnan University: Natural Sciences Edition, 2017, 39(6): 1035-1039. DOI: 10.7540/j.ynu.20170161

新颖一维链Zn配合物的合成、结构及荧光性质

Synthesis,structure and fluorescence of a novel 1D chain Zn coordination compound

  • 摘要: 以5,5-(ethane-1,2-diyl)-bis(oxy)diisophthalic acid为配体,采用溶剂热法合成一个单核新颖一维链Zn配合物Zn(H2edc)(H2O)3DMFn (1).通过X射线单晶衍射、元素分析、红外光谱和粉末衍射对其进行结构表征,并且研究了配合物的荧光性质.单晶解析表明,配合物1为三斜晶系P-1空间群,晶胞参数为a=0.71860(5)nm,b=1.25315(14)nm,c=1.29363(12)nm,=78.223(9),=88.372(7),=87.521(8).配合物1为由单核锌通过配体连接形成一维链结构,进而通过氢键连接为三维超分子结构.荧光测试表明,配合物1的发射光谱较配体的发射光谱有明显的红移,这是由于配体到金属Zn2+的电荷迁移所致.

     

    Abstract: A novel 1D chain compound with the formula Zn(H2edc)(H2O)3DMFn (1) has been synthesized by solvothermal method of the Zn(NO3)26H2O and 5,5-(ethane-1,2-diyl-bis(oxy)diisophthalic acid (H4edc).The compound has been characterized by single-crystal X-ray diffraction,elemental analyses,Fourier transform infrared (FT-IR) spectra and powder X-ray diffraction (PXRD),and the fluorescence of compound 1 was studied.Compound 1 belongs to triclinic P-1 space group,and the cell parameters a=0.71860(5)nm,b=1.25315(14)nm,c=1.29363(12)nm,=78.223(9),=88.372(7),and =87.521(8).The structure of compound 1 is a 1D chain which is formed by mononuclear Zn ion linked by H4edc ligands,and forming a 3D supermolecular structure by hydrogen bonds.Fluorescence research shows that the emission spectrum of compound 1 occurs large red shift compared with H4edc ligand,owing to the ligand-to-metal Zn2+ charge transfer.

     

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