镧系元素
化学
离子半径
结晶
金属有机骨架
选择性
配体(生物化学)
金属
格式化
无机化学
离子键合
甲酸钠
结晶学
物理化学
有机化学
离子
催化作用
吸附
受体
生物化学
作者
Xiang Zhao,Matthew S. Wong,Chengyu Mao,Thuong Xinh Trieu,Jian Zhang,Pingyun Feng,Xianhui Bu
摘要
Lanthanides (Ln) are a group of important elements usually found in nature as mixtures. Their separation is essential for technological applications but is made challenging by their subtly different properties. Here we report that crystallization of homochiral camphorate metal-organic frameworks (MOFs) is highly sensitive to ionic radii of lanthanides and can be used to selectively crystallize a lanthanide element into predesigned MOFs. Two series of camphorate MOFs were synthesized with acetate (Type 1 with early lanthanides La-Dy) or formate (Type 2 with late lanthanides Tb-Lu and Y) as the auxiliary ligand, respectively. The Ln coordination environment in each type exhibits selectivity for Ln(3+) of different sizes, which could form the basis for a new cost-effective method for Ln separation.
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