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 CO2activation, a record-high Brunauer-Emmett-Teller (BET) surface area (2100 m2g−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.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 10358-10362 |
| Number of pages | 5 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 55 |
| Issue number | 35 |
| DOIs | |
| State | Published - Aug 22 2016 |
Keywords
- enzyme separation
- ion exchange
- metal–organic frameworks
- uranium
- water-stable MOFs
ASJC Scopus subject areas
- Catalysis
- General Chemistry