金属有机骨架
铀
介孔材料
离子键合
离子交换
锕系元素
超临界流体
化学工程
生物分子
材料科学
无机化学
金属
离子
纳米技术
化学
有机化学
吸附
催化作用
工程类
冶金
作者
Peng Li,Nicolaas A. Vermeulen,Xirui Gong,Christos D. Malliakas,James Fraser Stoddart,Joseph T. Hupp,Omar K. Farha
标识
DOI:10.1002/ange.201605547
摘要
Abstract Ionic metal–organic frameworks (MOFs) are a subclass of porous materials that have the ability to incorporate different charged species in confined nanospace by ion‐exchange. To date, however, very few examples combining mesoporosity and water stability have been realized in ionic MOF chemistry. Herein, we report the rational design and synthesis of a water‐stable anionic mesoporous MOF based on uranium and featuring tbo‐type topology. The resulting tbo MOF exhibits exceptionally large open cavities (3.9 nm) exceeding those of all known anionic MOFs. By supercritical CO2 activation, a record‐high Brunauer‐Emmett‐Teller (BET) surface area (2100 m2 g−1) for actinide‐based MOFs has been obtained. Most importantly, however, this new uranium‐based MOF is water‐stable and able to absorb positively charged ions selectively over negatively charged ones, enabling the efficient separation of organic dyes and biomolecules.
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