| Literature DB >> 33666323 |
Jaewoong Lim1, Seonghwan Lee1, Hyeonbin Ha2, Junmo Seong1, Seok Jeong1, Min Kim2, Seung Bin Baek1, Myoung Soo Lah1.
Abstract
MOF-74 is one of the most explored metal-organic frameworks (MOFs), but its functionalization is limited to the dative post-synthetic modification (PSM) of the monodentate solvent site. Owing to the nature of the organic ligand and framework structure of MOF-74, the covalent PSM of MOF-74 is very demanding. Herein, we report, for the first time, the covalent PSM of amine-tagged defective Ni-MOF-74, which is prepared by de novo solvothermal synthesis by using aminosalicylic acid as a functionalized fragmented organic ligand. The covalent PSM of the amino group generates metal binding sites, and subsequent post-synthetic metalation with PdII ions affords the PdII -incorporated Ni-MOF-74 catalyst. This catalyst exhibits highly efficient, size-selective, and recyclable catalytic activity for the Suzuki-Miyaura cross-coupling reaction. This strategy is also useful for the covalent modification of amine-tagged defective Ni2 (DOBPDC), an expanded analogue of MOF-74.Entities:
Keywords: covalent modification; fragmented ligands; heterogeneous catalysis; metal-organic frameworks; post-synthetic modification
Year: 2021 PMID: 33666323 DOI: 10.1002/anie.202100456
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336