镧系元素
等结构
化学
金属有机骨架
发光
兴奋剂
离子
金属
无机化学
水溶液中的金属离子
光化学
物理化学
结晶学
晶体结构
有机化学
材料科学
光电子学
吸附
作者
Qun Tang,Shuxia Liu,Yiwei Liu,Duanwei He,Jun Miao,Xingquan Wang,Yujuan Ji,Zhiping Zheng
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2013-12-13
卷期号:53 (1): 289-293
被引量:197
摘要
Isostructural lanthanide metal–organic frameworks (MOFs) are synthesized through the spontaneous self-assembly of H3BTPCA (1,1′,1″-(benzene-1,3,5-triyl)tripiperidine-4-carboxylic acid) ligands and lanthanide ions (we term these MOFs Ln-BTPCA, Ln = La3+, Tb3+, Sm3+, etc.). Prompted by the observation that the different lanthanide ions have identical coordination environment in these MOFs, we explored and succeeded in the preparation of mixed-lanthanide analogues of the single-lanthanide MOFs by way of in situ doping using a mixture of lanthanide salts. With careful adjustment of the relative concentration of the lanthanide ions, the color of the luminescence can be modulated, and white light-emission can indeed be achieved. The mechanisms possibly responsible for the observed photophysical properties of these mixed-lanthanide MOFs are also discussed.
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