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Gold nanoparticle decorated post-synthesis modified UiO-66-NH(2) for A(3)-coupling preparation of propargyl amines

In this report, the novel UiO‑66‑NH(2) based-MOF(Zr) catalytic system which further modified with nitrogen-rich organic ligand (5-aminotetrazole) using post synthetic modification (PSM) approach has been prepared here as an efficient catalyst to promote the A(3)-coupling preparation of propargyl ami...

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Autores principales: Mohammadi, Leila, Taghavi, Reza, Hosseinifard, Mojtaba, Vaezi, Mohammad Reza, Rostamnia, Sadegh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10239494/
https://www.ncbi.nlm.nih.gov/pubmed/37270660
http://dx.doi.org/10.1038/s41598-023-35848-4
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author Mohammadi, Leila
Taghavi, Reza
Hosseinifard, Mojtaba
Vaezi, Mohammad Reza
Rostamnia, Sadegh
author_facet Mohammadi, Leila
Taghavi, Reza
Hosseinifard, Mojtaba
Vaezi, Mohammad Reza
Rostamnia, Sadegh
author_sort Mohammadi, Leila
collection PubMed
description In this report, the novel UiO‑66‑NH(2) based-MOF(Zr) catalytic system which further modified with nitrogen-rich organic ligand (5-aminotetrazole) using post synthetic modification (PSM) approach has been prepared here as an efficient catalyst to promote the A(3)-coupling preparation of propargyl amines in green aquatic media. This newly highly efficient catalyst was synthesized upon Zr-based MOF (UiO‑66‑NH(2)) which successfully functionalized with 2,4,6‑trichloro‑1,3,5‑triazine (TCT) and 5‑aminotetrazole, following through stabilization of gold metal (Au) nanopartilces. The addition of N-rich organic ligand through post-synthesis modification which can be assisted to stabilize the bister and stable gold nanoparticles caused to unique structure of the final composite in favor of the progress of the A(3) coupling reaction. Also several strategies comprising XRD, FT-IR, SEM, BET, TEM, TGA, ICP, EDS and elemental mapping analyzes, were used to indicate the successful preparation of the UiO-66-NH(2)@ Cyanuric Chloride@ 5-amino tetrazole/Au-NPs. The results of productivity catalyst are accomplished in good to excellent yields for all sort of reactions under mild conditions which is a proof of superior activity heterogeneous catalyst containing Au-nanoparticles. In addition, the suggested catalyst represented excellent reusability with no remarkable loss in activity up 9 sequential runs.
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spelling pubmed-102394942023-06-05 Gold nanoparticle decorated post-synthesis modified UiO-66-NH(2) for A(3)-coupling preparation of propargyl amines Mohammadi, Leila Taghavi, Reza Hosseinifard, Mojtaba Vaezi, Mohammad Reza Rostamnia, Sadegh Sci Rep Article In this report, the novel UiO‑66‑NH(2) based-MOF(Zr) catalytic system which further modified with nitrogen-rich organic ligand (5-aminotetrazole) using post synthetic modification (PSM) approach has been prepared here as an efficient catalyst to promote the A(3)-coupling preparation of propargyl amines in green aquatic media. This newly highly efficient catalyst was synthesized upon Zr-based MOF (UiO‑66‑NH(2)) which successfully functionalized with 2,4,6‑trichloro‑1,3,5‑triazine (TCT) and 5‑aminotetrazole, following through stabilization of gold metal (Au) nanopartilces. The addition of N-rich organic ligand through post-synthesis modification which can be assisted to stabilize the bister and stable gold nanoparticles caused to unique structure of the final composite in favor of the progress of the A(3) coupling reaction. Also several strategies comprising XRD, FT-IR, SEM, BET, TEM, TGA, ICP, EDS and elemental mapping analyzes, were used to indicate the successful preparation of the UiO-66-NH(2)@ Cyanuric Chloride@ 5-amino tetrazole/Au-NPs. The results of productivity catalyst are accomplished in good to excellent yields for all sort of reactions under mild conditions which is a proof of superior activity heterogeneous catalyst containing Au-nanoparticles. In addition, the suggested catalyst represented excellent reusability with no remarkable loss in activity up 9 sequential runs. Nature Publishing Group UK 2023-06-03 /pmc/articles/PMC10239494/ /pubmed/37270660 http://dx.doi.org/10.1038/s41598-023-35848-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Mohammadi, Leila
Taghavi, Reza
Hosseinifard, Mojtaba
Vaezi, Mohammad Reza
Rostamnia, Sadegh
Gold nanoparticle decorated post-synthesis modified UiO-66-NH(2) for A(3)-coupling preparation of propargyl amines
title Gold nanoparticle decorated post-synthesis modified UiO-66-NH(2) for A(3)-coupling preparation of propargyl amines
title_full Gold nanoparticle decorated post-synthesis modified UiO-66-NH(2) for A(3)-coupling preparation of propargyl amines
title_fullStr Gold nanoparticle decorated post-synthesis modified UiO-66-NH(2) for A(3)-coupling preparation of propargyl amines
title_full_unstemmed Gold nanoparticle decorated post-synthesis modified UiO-66-NH(2) for A(3)-coupling preparation of propargyl amines
title_short Gold nanoparticle decorated post-synthesis modified UiO-66-NH(2) for A(3)-coupling preparation of propargyl amines
title_sort gold nanoparticle decorated post-synthesis modified uio-66-nh(2) for a(3)-coupling preparation of propargyl amines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10239494/
https://www.ncbi.nlm.nih.gov/pubmed/37270660
http://dx.doi.org/10.1038/s41598-023-35848-4
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