Angewandte Chemie International Edition · 2021 · 62 citations · 33 references
Natural SciencesChemical EngineeringChemistryCatalysisInorganic ChemistryOrganometallic ChemistryCatalyst DesignCoordination ChemistryLigand BindingMetal-ligand BondingCatalytic ActivityCatalytic FunctionalizationLigand SelectivityMetal-organic Framework CatalystsMetal-organic Framework SynthesisMetal-organic FrameworksSolvothermal SynthesisSuzuki - Miyaura Coupling
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 Pd II ions affords the Pd II ‐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 Ni 2 (DOBPDC), an expanded analogue of MOF‐74.
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Cooperative insertion of CO2 in diamine-appended metal-organic frameworks
Thomas M. McDonald, Jarad A. Mason, Xueqian Kong et al. · Nature · 2015 · 1.3K citations · Full text
Thomas M. McDonald, Woo Ram Lee, Jarad A. Mason et al. · Journal of the American Chemical Society · 2012 · 1.3K citations