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Preparation and catalytic application of two different nanocatalysts based on hexagonal mesoporous silica (HMS) in synthesis of tetrahydrobenzo[b]pyran and 1,4-dihydropyrano[2,3-c]pyrazole derivatives

The present study describes the synthesis, characterization, and investigation of catalytic activity of xanthine-Ni complex (Xa-Ni) and 4-phenylthiosemicarbazide-Cu complex (PTSC-Cu) incorporated into functionalized hexagonal mesoporous silica (HMS/Pr-Xa-Ni and HMS/Pr-PTSC-Cu). These useful mesoporo...

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Autores principales: Abdolahi, Sahar, Gholamian, Fatemeh, Hajjami, Maryam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9772405/
https://www.ncbi.nlm.nih.gov/pubmed/36543926
http://dx.doi.org/10.1038/s41598-022-26605-0
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author Abdolahi, Sahar
Gholamian, Fatemeh
Hajjami, Maryam
author_facet Abdolahi, Sahar
Gholamian, Fatemeh
Hajjami, Maryam
author_sort Abdolahi, Sahar
collection PubMed
description The present study describes the synthesis, characterization, and investigation of catalytic activity of xanthine-Ni complex (Xa-Ni) and 4-phenylthiosemicarbazide-Cu complex (PTSC-Cu) incorporated into functionalized hexagonal mesoporous silica (HMS/Pr-Xa-Ni and HMS/Pr-PTSC-Cu). These useful mesoporous catalysts had been synthesized and identified using various techniques such as FT-IR, XRD, adsorption–desorption of nitrogen, SEM, TEM, EDX-Map, TGA, AAS and ICP. These spectral techniques successfully confirmed the synthesis of the mesoporous catalysts. The catalytic activity of HMS/Pr-a-Ni (Catalyst A) and HMS/Pr-PTSC-Cu (Catalyst B) were evaluated for synthesis of tetrahydrobenzo[b]pyran and 1,4-dihydropyrano[2,3-c]pyrazole derivatives. HMS/Pr-PTSC-Cu exhibited higher efficiency in green media under milder reaction condition at room temperature. Furthermore, the synthesized nanocatalysts, exhibited appropriate recoverability that can be able to reuse for several times without significant loss of catalytic activity.
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spelling pubmed-97724052022-12-23 Preparation and catalytic application of two different nanocatalysts based on hexagonal mesoporous silica (HMS) in synthesis of tetrahydrobenzo[b]pyran and 1,4-dihydropyrano[2,3-c]pyrazole derivatives Abdolahi, Sahar Gholamian, Fatemeh Hajjami, Maryam Sci Rep Article The present study describes the synthesis, characterization, and investigation of catalytic activity of xanthine-Ni complex (Xa-Ni) and 4-phenylthiosemicarbazide-Cu complex (PTSC-Cu) incorporated into functionalized hexagonal mesoporous silica (HMS/Pr-Xa-Ni and HMS/Pr-PTSC-Cu). These useful mesoporous catalysts had been synthesized and identified using various techniques such as FT-IR, XRD, adsorption–desorption of nitrogen, SEM, TEM, EDX-Map, TGA, AAS and ICP. These spectral techniques successfully confirmed the synthesis of the mesoporous catalysts. The catalytic activity of HMS/Pr-a-Ni (Catalyst A) and HMS/Pr-PTSC-Cu (Catalyst B) were evaluated for synthesis of tetrahydrobenzo[b]pyran and 1,4-dihydropyrano[2,3-c]pyrazole derivatives. HMS/Pr-PTSC-Cu exhibited higher efficiency in green media under milder reaction condition at room temperature. Furthermore, the synthesized nanocatalysts, exhibited appropriate recoverability that can be able to reuse for several times without significant loss of catalytic activity. Nature Publishing Group UK 2022-12-21 /pmc/articles/PMC9772405/ /pubmed/36543926 http://dx.doi.org/10.1038/s41598-022-26605-0 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
Abdolahi, Sahar
Gholamian, Fatemeh
Hajjami, Maryam
Preparation and catalytic application of two different nanocatalysts based on hexagonal mesoporous silica (HMS) in synthesis of tetrahydrobenzo[b]pyran and 1,4-dihydropyrano[2,3-c]pyrazole derivatives
title Preparation and catalytic application of two different nanocatalysts based on hexagonal mesoporous silica (HMS) in synthesis of tetrahydrobenzo[b]pyran and 1,4-dihydropyrano[2,3-c]pyrazole derivatives
title_full Preparation and catalytic application of two different nanocatalysts based on hexagonal mesoporous silica (HMS) in synthesis of tetrahydrobenzo[b]pyran and 1,4-dihydropyrano[2,3-c]pyrazole derivatives
title_fullStr Preparation and catalytic application of two different nanocatalysts based on hexagonal mesoporous silica (HMS) in synthesis of tetrahydrobenzo[b]pyran and 1,4-dihydropyrano[2,3-c]pyrazole derivatives
title_full_unstemmed Preparation and catalytic application of two different nanocatalysts based on hexagonal mesoporous silica (HMS) in synthesis of tetrahydrobenzo[b]pyran and 1,4-dihydropyrano[2,3-c]pyrazole derivatives
title_short Preparation and catalytic application of two different nanocatalysts based on hexagonal mesoporous silica (HMS) in synthesis of tetrahydrobenzo[b]pyran and 1,4-dihydropyrano[2,3-c]pyrazole derivatives
title_sort preparation and catalytic application of two different nanocatalysts based on hexagonal mesoporous silica (hms) in synthesis of tetrahydrobenzo[b]pyran and 1,4-dihydropyrano[2,3-c]pyrazole derivatives
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9772405/
https://www.ncbi.nlm.nih.gov/pubmed/36543926
http://dx.doi.org/10.1038/s41598-022-26605-0
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