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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...

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Autores principales: Bikas, Samaneh, Poursattar Marjani, Ahmad, Bibak, Sepideh, Sarreshtehdar Aslaheh, Hamideh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
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.
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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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