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Phosphonic acid tagged carbon quantum dots encapsulated in SBA-15 as a novel catalyst for the preparation of N-heterocycles with pyrazolo, barbituric acid and indole moieties
Herein, we have presented a new insight for the synthesis of a hybrid heterogeneous catalyst. For this purpose, phosphonic acid tagged carbon quantum dots of CQDs-N(CH(2)PO(3)H(2))(2) encapsulated and assembled in channels of SBA-15 using a post-modification strategy. The mesoporous catalyst of func...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9718821/ https://www.ncbi.nlm.nih.gov/pubmed/36460684 http://dx.doi.org/10.1038/s41598-022-24553-3 |
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author | Rasooll, Milad Mohammadi Sepehrmansourie, Hassan Zarei, Mahmoud Zolfigol, Mohammad Ali Rostamnia, Sadegh |
author_facet | Rasooll, Milad Mohammadi Sepehrmansourie, Hassan Zarei, Mahmoud Zolfigol, Mohammad Ali Rostamnia, Sadegh |
author_sort | Rasooll, Milad Mohammadi |
collection | PubMed |
description | Herein, we have presented a new insight for the synthesis of a hybrid heterogeneous catalyst. For this purpose, phosphonic acid tagged carbon quantum dots of CQDs-N(CH(2)PO(3)H(2))(2) encapsulated and assembled in channels of SBA-15 using a post-modification strategy. The mesoporous catalyst of functionalized carbon quantum dots (CQDs) was characterized by several techniques. CQDs-N(CH(2)PO(3)H(2))(2)/SBA-15 as an excellent catalyst was applied for the preparation of novel pyrazolo[4′,3′:5,6]pyrido[2,3-d]pyrimidine derivatives by using pyrazole, barbituric acid and indole moieties at 100 °C under the solvent-free condition. The present work shows that a significant increase in the catalytic activity can be achieved by a rational design of mesoporous SBA-15 modified with CQDs for the synthesis of biological active candidates. The synthesized compounds did not convert to their corresponding pyridines via an anomeric-based oxidation mechanism. |
format | Online Article Text |
id | pubmed-9718821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97188212022-12-04 Phosphonic acid tagged carbon quantum dots encapsulated in SBA-15 as a novel catalyst for the preparation of N-heterocycles with pyrazolo, barbituric acid and indole moieties Rasooll, Milad Mohammadi Sepehrmansourie, Hassan Zarei, Mahmoud Zolfigol, Mohammad Ali Rostamnia, Sadegh Sci Rep Article Herein, we have presented a new insight for the synthesis of a hybrid heterogeneous catalyst. For this purpose, phosphonic acid tagged carbon quantum dots of CQDs-N(CH(2)PO(3)H(2))(2) encapsulated and assembled in channels of SBA-15 using a post-modification strategy. The mesoporous catalyst of functionalized carbon quantum dots (CQDs) was characterized by several techniques. CQDs-N(CH(2)PO(3)H(2))(2)/SBA-15 as an excellent catalyst was applied for the preparation of novel pyrazolo[4′,3′:5,6]pyrido[2,3-d]pyrimidine derivatives by using pyrazole, barbituric acid and indole moieties at 100 °C under the solvent-free condition. The present work shows that a significant increase in the catalytic activity can be achieved by a rational design of mesoporous SBA-15 modified with CQDs for the synthesis of biological active candidates. The synthesized compounds did not convert to their corresponding pyridines via an anomeric-based oxidation mechanism. Nature Publishing Group UK 2022-12-02 /pmc/articles/PMC9718821/ /pubmed/36460684 http://dx.doi.org/10.1038/s41598-022-24553-3 Text en © The Author(s) 2022 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 Rasooll, Milad Mohammadi Sepehrmansourie, Hassan Zarei, Mahmoud Zolfigol, Mohammad Ali Rostamnia, Sadegh Phosphonic acid tagged carbon quantum dots encapsulated in SBA-15 as a novel catalyst for the preparation of N-heterocycles with pyrazolo, barbituric acid and indole moieties |
title | Phosphonic acid tagged carbon quantum dots encapsulated in SBA-15 as a novel catalyst for the preparation of N-heterocycles with pyrazolo, barbituric acid and indole moieties |
title_full | Phosphonic acid tagged carbon quantum dots encapsulated in SBA-15 as a novel catalyst for the preparation of N-heterocycles with pyrazolo, barbituric acid and indole moieties |
title_fullStr | Phosphonic acid tagged carbon quantum dots encapsulated in SBA-15 as a novel catalyst for the preparation of N-heterocycles with pyrazolo, barbituric acid and indole moieties |
title_full_unstemmed | Phosphonic acid tagged carbon quantum dots encapsulated in SBA-15 as a novel catalyst for the preparation of N-heterocycles with pyrazolo, barbituric acid and indole moieties |
title_short | Phosphonic acid tagged carbon quantum dots encapsulated in SBA-15 as a novel catalyst for the preparation of N-heterocycles with pyrazolo, barbituric acid and indole moieties |
title_sort | phosphonic acid tagged carbon quantum dots encapsulated in sba-15 as a novel catalyst for the preparation of n-heterocycles with pyrazolo, barbituric acid and indole moieties |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9718821/ https://www.ncbi.nlm.nih.gov/pubmed/36460684 http://dx.doi.org/10.1038/s41598-022-24553-3 |
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