| Home > Publications database > Enhanced Organocatalytic Processes through an Engineered Acid‐Base Site Bifunctional Pore in a Zirconium Metal‐Organic Framework |
| Journal Article | PUBDB-2024-08060 |
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2024
Wiley-VCH
Weinheim
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Please use a persistent id in citations: doi:10.1002/cctc.202400676 doi:10.3204/PUBDB-2024-08060
Abstract: This work introduces a robust acid-base catalytic system based on the zirconium-based metal-organic framework (Zr-MOF) MOF-808, selected for its open structure, high stability, and low presence of structural defects compared to other Zr-MOFs. Four bifunctional benzoate ligands bearing free carboxylic acid (-COOH) and nitrogen-containing groups were introduced into the MOF-808 using solvent-assisted ligand exchange methods. Unlike other materials, the acid and base sites in the bifunctional MOF-808 materials are situated in the same capping ligand, leading to a bifunctional behavior between the two neighboring sites. The system was tested for Knoevenagel condensation and deacetylation-Knoevenagel tandem reactions, demonstrating high catalytic activity and excellent yields. Additionally, computational modeling provided insights into the catalytic mechanism and the role of the acid-base sites. The study provides a better understanding of the unique behavior of the bifunctional MOF-808 catalyst and offers prospects for designing new and efficient catalytic systems for organocatalysis.
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