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Synthesis of spiroindenopyridazine-4H-pyran derivatives using Cr-based catalyst complexes supported on KCC-1 in aqueous solution
An efficient bis(2-dodecylsulfanyl-ethyl)-amine·CrCl(3) complex supported on KCC-1 (KCC-1/SNS/Cr) has been developed for the synthesis of spiroindenopyridazine-4H-pyran, providing excellent yields of the corresponding products with remarkable chemoselectivity. This morphology ultimately leads to hig...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078273/ https://www.ncbi.nlm.nih.gov/pubmed/35540387 http://dx.doi.org/10.1039/c7ra12871a |
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author | Zhiani, Rahele Sadeghzadeh, Seyed Mohsen Emrani, Shokufe |
author_facet | Zhiani, Rahele Sadeghzadeh, Seyed Mohsen Emrani, Shokufe |
author_sort | Zhiani, Rahele |
collection | PubMed |
description | An efficient bis(2-dodecylsulfanyl-ethyl)-amine·CrCl(3) complex supported on KCC-1 (KCC-1/SNS/Cr) has been developed for the synthesis of spiroindenopyridazine-4H-pyran, providing excellent yields of the corresponding products with remarkable chemoselectivity. This morphology ultimately leads to higher catalytic activity for the KCC-1-supported nanoparticles. The KCC-1/SNS/Cr NPs were thoroughly characterized by using TEM, SEM, TGA, FT-IR, ICP-MS, and BET. The recycled catalyst has been analyzed by ICP-MS showing only minor changes in morphology after the reaction, thus confirming the robustness of the catalyst. |
format | Online Article Text |
id | pubmed-9078273 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90782732022-05-09 Synthesis of spiroindenopyridazine-4H-pyran derivatives using Cr-based catalyst complexes supported on KCC-1 in aqueous solution Zhiani, Rahele Sadeghzadeh, Seyed Mohsen Emrani, Shokufe RSC Adv Chemistry An efficient bis(2-dodecylsulfanyl-ethyl)-amine·CrCl(3) complex supported on KCC-1 (KCC-1/SNS/Cr) has been developed for the synthesis of spiroindenopyridazine-4H-pyran, providing excellent yields of the corresponding products with remarkable chemoselectivity. This morphology ultimately leads to higher catalytic activity for the KCC-1-supported nanoparticles. The KCC-1/SNS/Cr NPs were thoroughly characterized by using TEM, SEM, TGA, FT-IR, ICP-MS, and BET. The recycled catalyst has been analyzed by ICP-MS showing only minor changes in morphology after the reaction, thus confirming the robustness of the catalyst. The Royal Society of Chemistry 2018-02-07 /pmc/articles/PMC9078273/ /pubmed/35540387 http://dx.doi.org/10.1039/c7ra12871a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Zhiani, Rahele Sadeghzadeh, Seyed Mohsen Emrani, Shokufe Synthesis of spiroindenopyridazine-4H-pyran derivatives using Cr-based catalyst complexes supported on KCC-1 in aqueous solution |
title | Synthesis of spiroindenopyridazine-4H-pyran derivatives using Cr-based catalyst complexes supported on KCC-1 in aqueous solution |
title_full | Synthesis of spiroindenopyridazine-4H-pyran derivatives using Cr-based catalyst complexes supported on KCC-1 in aqueous solution |
title_fullStr | Synthesis of spiroindenopyridazine-4H-pyran derivatives using Cr-based catalyst complexes supported on KCC-1 in aqueous solution |
title_full_unstemmed | Synthesis of spiroindenopyridazine-4H-pyran derivatives using Cr-based catalyst complexes supported on KCC-1 in aqueous solution |
title_short | Synthesis of spiroindenopyridazine-4H-pyran derivatives using Cr-based catalyst complexes supported on KCC-1 in aqueous solution |
title_sort | synthesis of spiroindenopyridazine-4h-pyran derivatives using cr-based catalyst complexes supported on kcc-1 in aqueous solution |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078273/ https://www.ncbi.nlm.nih.gov/pubmed/35540387 http://dx.doi.org/10.1039/c7ra12871a |
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