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Stabilization of Palladium-Nanoparticle-Decorated Postsynthesis-Modified Zr-UiO-66 MOF as a Reusable Heterogeneous Catalyst in C–C Coupling Reaction
[Image: see text] Here we prepared a highly efficient and reusable catalyst by a step-by-step postsynthesis modification of UiO-66-NH(2) metal–organic frameworks (MOFs) with nitrogen-rich organic ligands and used it as support for the preparation of UiO-66-NH(2)@cyanuric chloride@2-aminopyrimidine/P...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9996586/ https://www.ncbi.nlm.nih.gov/pubmed/36910943 http://dx.doi.org/10.1021/acsomega.2c07661 |
Sumario: | [Image: see text] Here we prepared a highly efficient and reusable catalyst by a step-by-step postsynthesis modification of UiO-66-NH(2) metal–organic frameworks (MOFs) with nitrogen-rich organic ligands and used it as support for the preparation of UiO-66-NH(2)@cyanuric chloride@2-aminopyrimidine/Pd(NPs). The catalytic performance’s results of UiO-66-NH(2)@cyanuric chloride@2-aminopyrimidine/PdNPs, UiO-66-NH(2)/PdNPs, and UiO-66-NH(2)@cyanuric chloride/PdNPs indicate high efficiency of the modulation of the microenvironment of the palladium NPs. The addition of N-rich organic ligands through postsynthesis modification caused a unique structure of the final composite in favor of the progress of the C–C coupling reaction. Various techniques, including FT-IR, XRD, SEM, TEM, EDS, and elemental mapping, were used to characterize UiO-66-NH(2)@cyanuric chloride@2-aminopyrimidine/Pd(NPs), indicating its successful preparation. Three C–C coupling reactions, including the Suzuki, Heck, and Sonogashira coupling reactions, were promoted using the produced catalyst. As a result of the postsynthesis modification (PSM), the proposed catalyst displays improved catalytic performance. In addition, the suggested catalyst was highly recyclable up to ten times without leaching of PdNPs. |
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