Hydrophobic B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>@R<sub>4</sub>-MIL-101: A Water-Resistant Heterogeneous Catalyst for Frustrated Lewis Pairs-Mediated Reductive Amination
B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-based frustrated Lewis pairs (FLPs) have made remarkable progress in metal-free catalytic reduction. However, the high affinity of B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub> for oxygen makes it susceptible to irreversible poisoning when exposed to H<sub>2</sub>O, limiting its widespread application in reductive amination. To overcome the influence of H<sub>2</sub>O, a hydrophobic catalyst, B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>@R<sub><i>n-</i>1</sub>-MIL-101 (<i>n</i> = 3, 5, 7), was developed by confining B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub> within the nanocages of metal-organic frameworks (MOFs) modified with alkyl chains. The hydrophobic strength of the catalyst could be adjusted by varying the length of the alkyl chain. At <i>n</i> = 3, the alkyl chain was too short to be hydrophobic, while the excessively long alkyl chain blocked the pore channels and adversely affected the loading of B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub> at <i>n</i> = 7. Only the catalyst B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>@R<sub>4</sub>-MIL-101 synthesized at <i>n</i> = 5 could effectively facilitate the reductive amination of aldehydes or ketones with amines in a "wet solvent." The strategy of combining hydrophobic MOFs with B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub> to prepare heterogeneous catalysts for FLP catalysis not only provides a fresh avenue for investigating catalytic systems for reductive amination but also represents an innovative approach to advancing FLP chemistry.
Authors
- Liang Yan (ORCID: https://orcid.org/0000-0002-5062-2540)
- Miaomiao Chen (ORCID: https://orcid.org/0000-0002-7265-1801)
- Min Ji (ORCID: https://orcid.org/0000-0002-0971-550X)
- Huili Zhao
- Min Wang (ORCID: https://orcid.org/0000-0002-9072-8331)
- Xue Han
Institutions
- Dalian University of Technology (CN)
- Dalian University (CN)
Publication Details
- Journal
- Inorganic Chemistry
- Published
- 2025-03-24
- DOI
- https://doi.org/10.1021/acs.inorgchem.4c04665
- Citations
- 1
- Primary Topic
- Organoboron and organosilicon chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.94
Funders
- National Natural Science Foundation of China
- Fundamental Research Funds for the Central Universities