Selective Crystallization of Rare-Earth Ions into Cationic Metal-Organic Frameworks for Rare-Earth Separation

被引:39
|
作者
Yang, Huajun [1 ,2 ]
Peng, Fang [1 ]
Schier, Danielle E. [1 ]
Markotic, Stipe A. [1 ]
Zhao, Xiang [2 ]
Hong, Anh N. [2 ]
Wang, Yanxiang [2 ]
Feng, Pingyun [2 ]
Bu, Xianhui [1 ]
机构
[1] Calif State Univ Long Beach, Dept Chem & Biochem, Long Beach, CA 90840 USA
[2] Univ Calif Riverside, Dept Chem, Riverside, CA 92521 USA
基金
美国国家科学基金会;
关键词
low-coordination number; MOFs; rare-earth separation; trimer; urea solvents;
D O I
10.1002/anie.202017042
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
For rare-earth separation, selective crystallization into metal-organic frameworks (MOFs) offers new opportunities. Especially important is the development of MOF platforms with high selectivity toward target ions. Here we report a MOF platform (CPM-66) with low-coordination-number environment for rare-earth ions. This platform is highly responsive to the size variation of rare-earth ions and shows exceptional ion-size selectivity during crystallization. CPM-66 family are based on M3O trimers (M=6-coordinated Sc, In, Er-Lu) that are rare for lanthanides. We show that the size matching between urea-type solvents and metal ions is crucial for their successful synthesis. We further show that CPM-66 enables a dramatic multi-fold increase in separation efficiency over CPM-29 with 7-coordinated ions. This work provides some insights into methods to prepare low-coordinate MOFs from large ions and such MOFs could serve as high-efficiency platforms for lanthanide separation, as well as other applications.
引用
收藏
页码:11148 / 11152
页数:5
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