Abstract
The covalent modification of the metal−organic framework IRMOF-3 has been achieved using acetic anhydride. Mass spectrometry and 1H NMR evidence shows that the free amine groups in IRMOF-3 are converted to amides in high yields. Control experiments and X-ray diffraction studies suggest that this reaction occurs on the intact framework with preservation of crystallinity. This finding opens up new possibilities for the preparation of novel MOFs using a postsynthetic modification strategy.
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Publication Info
- Year
- 2007
- Type
- article
- Volume
- 129
- Issue
- 41
- Pages
- 12368-12369
- Citations
- 616
- Access
- Closed
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Identifiers
- DOI
- 10.1021/ja074366o