化学
镧系元素
催化作用
肉眼
配体(生物化学)
选择性
金属有机骨架
发光
结晶学
晶体结构
光化学
离子
有机化学
受体
材料科学
吸附
检出限
生物化学
光电子学
色谱法
作者
Pengyan Wu,Lingling Xia,Mengjie Huangfu,Fubin Fu,Mengqiu Wang,Bingxin Wen,Ziyun Yang,Jian Wang
标识
DOI:10.1021/acs.inorgchem.9b02177
摘要
Three lanthanide-based metal–organic frameworks, [Tb(HMDIA)(H2O)3]·H2O (Tb-MDIA), [Ho(HMDIA)(H2O)3]·(H2O)2 (Ho-MDIA), and [Nd(HMDIA)(H2O)3]·(H2O)2 (Nd-MDIA) from the same V-shaped ligand 5,5′-methylenediisophthalic acid (H4MDIA), were prepared by mixing Ln3+ and H4MDIA under solvothermal conditions. The crystal structures of the three complexes were determined by single-crystal X-ray diffraction. The different coordination modes of the organic ligands resulted in different framework structures among the three complexes. The luminescent properties of Ln-MDIA in the ultraviolet–visible region were also studied. Interestingly, the bright-green emitter Tb-MDIA showed high selectivity and sensitivity to allow the naked-eye visualization of Fe3+ ions and picric acid (PA) explosive, and both sensing mechanisms were revealed. Finally, Ho-MDIA and Nd-MDIA were shown to work as heterogeneous catalysts for the cyanosilylation reaction of aromatic aldehydes, and the catalysts could be recycled at least three times without any decrease in activity.
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