Cargando…
Highly Selective Synthesis of Hydrazoarenes from Nitroarenes via Polystyrene-Supported Au-Nanoparticle-Catalyzed Reduction: Application to Azoarenes, Aminoarenes, and 4,4′-Diaminobiaryls
[Image: see text] A selective synthesis of hydrazoarene from nitroarene and its application are reported. Using polystyrene (PS) resins as solid supports for Au nanoparticles (AuNPs), polystyrene-supported Au nanoparticles (AuNPs@PS) were synthesized and characterized. In the presence of AuNPs@PS (1...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7144144/ https://www.ncbi.nlm.nih.gov/pubmed/32280901 http://dx.doi.org/10.1021/acsomega.0c00402 |
_version_ | 1783519779272785920 |
---|---|
author | Hong, Jee Eun Jung, Yeonghun Park, Youmie Park, Yohan |
author_facet | Hong, Jee Eun Jung, Yeonghun Park, Youmie Park, Yohan |
author_sort | Hong, Jee Eun |
collection | PubMed |
description | [Image: see text] A selective synthesis of hydrazoarene from nitroarene and its application are reported. Using polystyrene (PS) resins as solid supports for Au nanoparticles (AuNPs), polystyrene-supported Au nanoparticles (AuNPs@PS) were synthesized and characterized. In the presence of AuNPs@PS (1.0 mol %) as a catalyst, nitroarenes afforded corresponding hydrazoarenes (up to 99%) with high selectivity (up to 100%) under mild reaction conditions (NaBH(4), 50% aq. EtOH, and room temperature). Depending on the reaction conditions (the amount of NaBH(4), the substituent of nitroarenes, and the sequential addition of HCl), nitroarenes were converted to corresponding azoarenes (up to 95%), aminoarenes (up to 99%), and 4,4′-diaminobiaryls (up to 99%). Our easily recyclable catalytic system using a solid-phase reaction vessel provides an attractive synthetic method in an eco-friendly and sustainable manner. |
format | Online Article Text |
id | pubmed-7144144 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-71441442020-04-10 Highly Selective Synthesis of Hydrazoarenes from Nitroarenes via Polystyrene-Supported Au-Nanoparticle-Catalyzed Reduction: Application to Azoarenes, Aminoarenes, and 4,4′-Diaminobiaryls Hong, Jee Eun Jung, Yeonghun Park, Youmie Park, Yohan ACS Omega [Image: see text] A selective synthesis of hydrazoarene from nitroarene and its application are reported. Using polystyrene (PS) resins as solid supports for Au nanoparticles (AuNPs), polystyrene-supported Au nanoparticles (AuNPs@PS) were synthesized and characterized. In the presence of AuNPs@PS (1.0 mol %) as a catalyst, nitroarenes afforded corresponding hydrazoarenes (up to 99%) with high selectivity (up to 100%) under mild reaction conditions (NaBH(4), 50% aq. EtOH, and room temperature). Depending on the reaction conditions (the amount of NaBH(4), the substituent of nitroarenes, and the sequential addition of HCl), nitroarenes were converted to corresponding azoarenes (up to 95%), aminoarenes (up to 99%), and 4,4′-diaminobiaryls (up to 99%). Our easily recyclable catalytic system using a solid-phase reaction vessel provides an attractive synthetic method in an eco-friendly and sustainable manner. American Chemical Society 2020-03-27 /pmc/articles/PMC7144144/ /pubmed/32280901 http://dx.doi.org/10.1021/acsomega.0c00402 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Hong, Jee Eun Jung, Yeonghun Park, Youmie Park, Yohan Highly Selective Synthesis of Hydrazoarenes from Nitroarenes via Polystyrene-Supported Au-Nanoparticle-Catalyzed Reduction: Application to Azoarenes, Aminoarenes, and 4,4′-Diaminobiaryls |
title | Highly Selective Synthesis of Hydrazoarenes from Nitroarenes
via Polystyrene-Supported Au-Nanoparticle-Catalyzed Reduction: Application
to Azoarenes, Aminoarenes, and 4,4′-Diaminobiaryls |
title_full | Highly Selective Synthesis of Hydrazoarenes from Nitroarenes
via Polystyrene-Supported Au-Nanoparticle-Catalyzed Reduction: Application
to Azoarenes, Aminoarenes, and 4,4′-Diaminobiaryls |
title_fullStr | Highly Selective Synthesis of Hydrazoarenes from Nitroarenes
via Polystyrene-Supported Au-Nanoparticle-Catalyzed Reduction: Application
to Azoarenes, Aminoarenes, and 4,4′-Diaminobiaryls |
title_full_unstemmed | Highly Selective Synthesis of Hydrazoarenes from Nitroarenes
via Polystyrene-Supported Au-Nanoparticle-Catalyzed Reduction: Application
to Azoarenes, Aminoarenes, and 4,4′-Diaminobiaryls |
title_short | Highly Selective Synthesis of Hydrazoarenes from Nitroarenes
via Polystyrene-Supported Au-Nanoparticle-Catalyzed Reduction: Application
to Azoarenes, Aminoarenes, and 4,4′-Diaminobiaryls |
title_sort | highly selective synthesis of hydrazoarenes from nitroarenes
via polystyrene-supported au-nanoparticle-catalyzed reduction: application
to azoarenes, aminoarenes, and 4,4′-diaminobiaryls |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7144144/ https://www.ncbi.nlm.nih.gov/pubmed/32280901 http://dx.doi.org/10.1021/acsomega.0c00402 |
work_keys_str_mv | AT hongjeeeun highlyselectivesynthesisofhydrazoarenesfromnitroarenesviapolystyrenesupportedaunanoparticlecatalyzedreductionapplicationtoazoarenesaminoarenesand44diaminobiaryls AT jungyeonghun highlyselectivesynthesisofhydrazoarenesfromnitroarenesviapolystyrenesupportedaunanoparticlecatalyzedreductionapplicationtoazoarenesaminoarenesand44diaminobiaryls AT parkyoumie highlyselectivesynthesisofhydrazoarenesfromnitroarenesviapolystyrenesupportedaunanoparticlecatalyzedreductionapplicationtoazoarenesaminoarenesand44diaminobiaryls AT parkyohan highlyselectivesynthesisofhydrazoarenesfromnitroarenesviapolystyrenesupportedaunanoparticlecatalyzedreductionapplicationtoazoarenesaminoarenesand44diaminobiaryls |