纳米笼
铀酰
吸附
化学
金属有机骨架
配体(生物化学)
多孔性
铀
离子
介孔材料
结晶学
化学工程
无机化学
材料科学
吸附
物理化学
有机化学
催化作用
生物化学
受体
工程类
冶金
作者
Xiao‐Feng Wang,Yang‐Yang Chen,Liping Song,Zhen Fang,Jian Zhang,Fa‐Nian Shi,Ying‐Wu Lin,Yunkai Sun,Yue‐Biao Zhang,João Rocha
标识
DOI:10.1002/ange.201909045
摘要
Abstract To efficiently capture the toxic uranyl ions (UO 2 2+ ), a new hierarchical micro‐macroporous metal–organic framework was prepared under template‐free conditions, featuring interconnected multi‐nanocages bearing carbonyl groups derived from a semi‐rigid ligand. The material exhibits an unusually high UO 2 2+ sorption capacity of 562 mg g −1 , which occurs in an intriguing two‐steps process, on the macropore‐based crystal surface and in the inner nanocages. Notably, the latter is attributed to the cooperative interplay of the shrinkage of the host porous framework induced by uranyl accommodation and the free carbonyl coordination sites, as shown by both single‐crystal X‐ray diffraction and a red‐shift of the infrared [O=U VI =O] 2+ antisymmetric vibration band.
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