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Nitro to amine reductions using aqueous flow catalysis under ambient conditions

A catalyst based on Pd on glass wool (Pd@GW) shows exceptional performance and durability for the reduction of nitrobenzene to aniline at room temperature and ambient pressure in aqueous solutions. The reaction is performed in a flow system and completed with 100% conversion under a variety of flow...

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Autores principales: Yaghmaei, Mahzad, Lanterna, Anabel E., Scaiano, Juan C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8671935/
https://www.ncbi.nlm.nih.gov/pubmed/34950857
http://dx.doi.org/10.1016/j.isci.2021.103472
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author Yaghmaei, Mahzad
Lanterna, Anabel E.
Scaiano, Juan C.
author_facet Yaghmaei, Mahzad
Lanterna, Anabel E.
Scaiano, Juan C.
author_sort Yaghmaei, Mahzad
collection PubMed
description A catalyst based on Pd on glass wool (Pd@GW) shows exceptional performance and durability for the reduction of nitrobenzene to aniline at room temperature and ambient pressure in aqueous solutions. The reaction is performed in a flow system and completed with 100% conversion under a variety of flow rates, 2 to 100 mLmin(−1) (normal laboratory fast flow conditions). Sodium borohydride or dihydrogen perform well as reducing agents. Scale-up of the reaction to flows of 100 mLmin(−1) also shows high conversions and robust catalytic performance. Catalyst deactivation can be readily corrected by flowing a NaBH(4) solution. The catalytic system proves to be generally efficient, performing well with a range of nitroaromatic compounds. The shelf life of the catalyst is excellent and its reusability after 6-8 months of storage showed the same performance as for the fresh catalyst.
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spelling pubmed-86719352021-12-22 Nitro to amine reductions using aqueous flow catalysis under ambient conditions Yaghmaei, Mahzad Lanterna, Anabel E. Scaiano, Juan C. iScience Article A catalyst based on Pd on glass wool (Pd@GW) shows exceptional performance and durability for the reduction of nitrobenzene to aniline at room temperature and ambient pressure in aqueous solutions. The reaction is performed in a flow system and completed with 100% conversion under a variety of flow rates, 2 to 100 mLmin(−1) (normal laboratory fast flow conditions). Sodium borohydride or dihydrogen perform well as reducing agents. Scale-up of the reaction to flows of 100 mLmin(−1) also shows high conversions and robust catalytic performance. Catalyst deactivation can be readily corrected by flowing a NaBH(4) solution. The catalytic system proves to be generally efficient, performing well with a range of nitroaromatic compounds. The shelf life of the catalyst is excellent and its reusability after 6-8 months of storage showed the same performance as for the fresh catalyst. Elsevier 2021-11-18 /pmc/articles/PMC8671935/ /pubmed/34950857 http://dx.doi.org/10.1016/j.isci.2021.103472 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Yaghmaei, Mahzad
Lanterna, Anabel E.
Scaiano, Juan C.
Nitro to amine reductions using aqueous flow catalysis under ambient conditions
title Nitro to amine reductions using aqueous flow catalysis under ambient conditions
title_full Nitro to amine reductions using aqueous flow catalysis under ambient conditions
title_fullStr Nitro to amine reductions using aqueous flow catalysis under ambient conditions
title_full_unstemmed Nitro to amine reductions using aqueous flow catalysis under ambient conditions
title_short Nitro to amine reductions using aqueous flow catalysis under ambient conditions
title_sort nitro to amine reductions using aqueous flow catalysis under ambient conditions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8671935/
https://www.ncbi.nlm.nih.gov/pubmed/34950857
http://dx.doi.org/10.1016/j.isci.2021.103472
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