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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 |
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author | Mohammadi, Leila Hosseinifard, Mojtaba Vaezi, Mohammad Reza |
author_facet | Mohammadi, Leila Hosseinifard, Mojtaba Vaezi, Mohammad Reza |
author_sort | Mohammadi, Leila |
collection | PubMed |
description | [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. |
format | Online Article Text |
id | pubmed-9996586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-99965862023-03-10 Stabilization of Palladium-Nanoparticle-Decorated Postsynthesis-Modified Zr-UiO-66 MOF as a Reusable Heterogeneous Catalyst in C–C Coupling Reaction Mohammadi, Leila Hosseinifard, Mojtaba Vaezi, Mohammad Reza ACS Omega [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. American Chemical Society 2023-02-24 /pmc/articles/PMC9996586/ /pubmed/36910943 http://dx.doi.org/10.1021/acsomega.2c07661 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Mohammadi, Leila Hosseinifard, Mojtaba Vaezi, Mohammad Reza Stabilization of Palladium-Nanoparticle-Decorated Postsynthesis-Modified Zr-UiO-66 MOF as a Reusable Heterogeneous Catalyst in C–C Coupling Reaction |
title | Stabilization of
Palladium-Nanoparticle-Decorated
Postsynthesis-Modified Zr-UiO-66 MOF as a Reusable Heterogeneous Catalyst
in C–C Coupling Reaction |
title_full | Stabilization of
Palladium-Nanoparticle-Decorated
Postsynthesis-Modified Zr-UiO-66 MOF as a Reusable Heterogeneous Catalyst
in C–C Coupling Reaction |
title_fullStr | Stabilization of
Palladium-Nanoparticle-Decorated
Postsynthesis-Modified Zr-UiO-66 MOF as a Reusable Heterogeneous Catalyst
in C–C Coupling Reaction |
title_full_unstemmed | Stabilization of
Palladium-Nanoparticle-Decorated
Postsynthesis-Modified Zr-UiO-66 MOF as a Reusable Heterogeneous Catalyst
in C–C Coupling Reaction |
title_short | Stabilization of
Palladium-Nanoparticle-Decorated
Postsynthesis-Modified Zr-UiO-66 MOF as a Reusable Heterogeneous Catalyst
in C–C Coupling Reaction |
title_sort | stabilization of
palladium-nanoparticle-decorated
postsynthesis-modified zr-uio-66 mof as a reusable heterogeneous catalyst
in c–c coupling reaction |
url | 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 |
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