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Synthesis of new magnetic nanocatalyst Fe(3)O(4)@CPTMO-phenylalanine-Ni and its catalytic effect in the preparation of substituted pyrazoles
In this study, a new, efficient and stable magnetically heterogeneous nanocatalyst of Fe(3)O(4)@CPTMO-phenylalanine-Ni via multi steps process starting from simple and cost-effective precursors was designed and successfully synthesized, and physico-chemical, structural, and magnetic properties have...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9925813/ https://www.ncbi.nlm.nih.gov/pubmed/36781940 http://dx.doi.org/10.1038/s41598-023-29598-6 |
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author | Bikas, Samaneh Poursattar Marjani, Ahmad Bibak, Sepideh Sarreshtehdar Aslaheh, Hamideh |
author_facet | Bikas, Samaneh Poursattar Marjani, Ahmad Bibak, Sepideh Sarreshtehdar Aslaheh, Hamideh |
author_sort | Bikas, Samaneh |
collection | PubMed |
description | In this study, a new, efficient and stable magnetically heterogeneous nanocatalyst of Fe(3)O(4)@CPTMO-phenylalanine-Ni via multi steps process starting from simple and cost-effective precursors was designed and successfully synthesized, and physico-chemical, structural, and magnetic properties have fully been characterized by several analytical methods involving SEM–EDS, FT-IR, TGA, VSM, XRD, ICP, BET, TEM, and EMA. The catalytic performance of the Fe(3)O(4)@CPTMO-phenylalanine-Ni can be used as an effective and recyclable nanocatalyst with facile separation by magnetic forces for the preparation of substituted pyrazoles with high yields through the one-pot, three-component condensation reaction of various arylglyoxals, diketones, and 1H-pyrazole-5-amines under mild conditions. The nanocatalyst’s activity after being used by four consecutive times in a cycle reaction without distinct deterioration remained unchanged or was found to be a slight decrease. The advantages of this study are simplicity, low cost, facile synthesis process, and environmentally secure nature. |
format | Online Article Text |
id | pubmed-9925813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99258132023-02-15 Synthesis of new magnetic nanocatalyst Fe(3)O(4)@CPTMO-phenylalanine-Ni and its catalytic effect in the preparation of substituted pyrazoles Bikas, Samaneh Poursattar Marjani, Ahmad Bibak, Sepideh Sarreshtehdar Aslaheh, Hamideh Sci Rep Article In this study, a new, efficient and stable magnetically heterogeneous nanocatalyst of Fe(3)O(4)@CPTMO-phenylalanine-Ni via multi steps process starting from simple and cost-effective precursors was designed and successfully synthesized, and physico-chemical, structural, and magnetic properties have fully been characterized by several analytical methods involving SEM–EDS, FT-IR, TGA, VSM, XRD, ICP, BET, TEM, and EMA. The catalytic performance of the Fe(3)O(4)@CPTMO-phenylalanine-Ni can be used as an effective and recyclable nanocatalyst with facile separation by magnetic forces for the preparation of substituted pyrazoles with high yields through the one-pot, three-component condensation reaction of various arylglyoxals, diketones, and 1H-pyrazole-5-amines under mild conditions. The nanocatalyst’s activity after being used by four consecutive times in a cycle reaction without distinct deterioration remained unchanged or was found to be a slight decrease. The advantages of this study are simplicity, low cost, facile synthesis process, and environmentally secure nature. Nature Publishing Group UK 2023-02-13 /pmc/articles/PMC9925813/ /pubmed/36781940 http://dx.doi.org/10.1038/s41598-023-29598-6 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 Bikas, Samaneh Poursattar Marjani, Ahmad Bibak, Sepideh Sarreshtehdar Aslaheh, Hamideh Synthesis of new magnetic nanocatalyst Fe(3)O(4)@CPTMO-phenylalanine-Ni and its catalytic effect in the preparation of substituted pyrazoles |
title | Synthesis of new magnetic nanocatalyst Fe(3)O(4)@CPTMO-phenylalanine-Ni and its catalytic effect in the preparation of substituted pyrazoles |
title_full | Synthesis of new magnetic nanocatalyst Fe(3)O(4)@CPTMO-phenylalanine-Ni and its catalytic effect in the preparation of substituted pyrazoles |
title_fullStr | Synthesis of new magnetic nanocatalyst Fe(3)O(4)@CPTMO-phenylalanine-Ni and its catalytic effect in the preparation of substituted pyrazoles |
title_full_unstemmed | Synthesis of new magnetic nanocatalyst Fe(3)O(4)@CPTMO-phenylalanine-Ni and its catalytic effect in the preparation of substituted pyrazoles |
title_short | Synthesis of new magnetic nanocatalyst Fe(3)O(4)@CPTMO-phenylalanine-Ni and its catalytic effect in the preparation of substituted pyrazoles |
title_sort | synthesis of new magnetic nanocatalyst fe(3)o(4)@cptmo-phenylalanine-ni and its catalytic effect in the preparation of substituted pyrazoles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9925813/ https://www.ncbi.nlm.nih.gov/pubmed/36781940 http://dx.doi.org/10.1038/s41598-023-29598-6 |
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