Journal Article PUBDB-2024-08060

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Enhanced Organocatalytic Processes through an Engineered Acid‐Base Site Bifunctional Pore in a Zirconium Metal‐Organic Framework

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2024
Wiley-VCH Weinheim

ChemCatChem 16(18), e202400676 () [10.1002/cctc.202400676]
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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.

Classification:

Contributing Institute(s):
  1. DOOR-User (DOOR ; HAS-User)
Research Program(s):
  1. 6G3 - PETRA III (DESY) (POF4-6G3) (POF4-6G3)
  2. FS-Proposal: I-20211230 EC (I-20211230-EC) (I-20211230-EC)
Experiment(s):
  1. PETRA Beamline P02.1 (PETRA III)

Appears in the scientific report 2024
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 Record created 2024-12-23, last modified 2025-07-23


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