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A new bifunctional heterogeneous nanocatalyst for one-pot reduction-Schiff base condensation and reduction–carbonylation of nitroarenes
In this work, synthesis of Pd–NHC-γ-Fe(2)O(3)-n-butyl-SO(3)H and its activity as a bifunctional heterogeneous nanocatalyst containing Pd–NHC and acidic functional groups, are described. This newly synthesized nanomagnetic catalyst is fully characterized by different methods such as FT-IR, XPS, TEM,...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059666/ https://www.ncbi.nlm.nih.gov/pubmed/35518036 http://dx.doi.org/10.1039/c8ra10212k |
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author | Sobhani, Sara Chahkamali, Farhad Omarzehi Sansano, José Miguel |
author_facet | Sobhani, Sara Chahkamali, Farhad Omarzehi Sansano, José Miguel |
author_sort | Sobhani, Sara |
collection | PubMed |
description | In this work, synthesis of Pd–NHC-γ-Fe(2)O(3)-n-butyl-SO(3)H and its activity as a bifunctional heterogeneous nanocatalyst containing Pd–NHC and acidic functional groups, are described. This newly synthesized nanomagnetic catalyst is fully characterized by different methods such as FT-IR, XPS, TEM, VSM, ICP and TG analysis. At first, the catalytic activity of Pd–NHC-γ-Fe(2)O(3)-n-butyl-SO(3)H is evaluated for the reduction of nitroarenes in aqueous media using NaBH(4) as a clean source of hydrogen generation at ambient temperature. Using the promising results obtained from the nitroarene reduction, this catalytic system is used for two one-pot protocols including reduction-Schiff base condensation and reduction–carbonylation of various nitroarenes. In these reactions the in situ formed amines are further reacted with aldehydes to yield imines or carbonylated to amides. The desired products are obtained in good to high yields in the presence of Pd–NHC-γ-Fe(2)O(3)-n-butyl-SO(3)H as a bifunctional catalyst. The catalyst is reused with the aid of a magnetic bar for up to six consecutive cycles without any drastic loss of its catalytic activity. |
format | Online Article Text |
id | pubmed-9059666 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90596662022-05-04 A new bifunctional heterogeneous nanocatalyst for one-pot reduction-Schiff base condensation and reduction–carbonylation of nitroarenes Sobhani, Sara Chahkamali, Farhad Omarzehi Sansano, José Miguel RSC Adv Chemistry In this work, synthesis of Pd–NHC-γ-Fe(2)O(3)-n-butyl-SO(3)H and its activity as a bifunctional heterogeneous nanocatalyst containing Pd–NHC and acidic functional groups, are described. This newly synthesized nanomagnetic catalyst is fully characterized by different methods such as FT-IR, XPS, TEM, VSM, ICP and TG analysis. At first, the catalytic activity of Pd–NHC-γ-Fe(2)O(3)-n-butyl-SO(3)H is evaluated for the reduction of nitroarenes in aqueous media using NaBH(4) as a clean source of hydrogen generation at ambient temperature. Using the promising results obtained from the nitroarene reduction, this catalytic system is used for two one-pot protocols including reduction-Schiff base condensation and reduction–carbonylation of various nitroarenes. In these reactions the in situ formed amines are further reacted with aldehydes to yield imines or carbonylated to amides. The desired products are obtained in good to high yields in the presence of Pd–NHC-γ-Fe(2)O(3)-n-butyl-SO(3)H as a bifunctional catalyst. The catalyst is reused with the aid of a magnetic bar for up to six consecutive cycles without any drastic loss of its catalytic activity. The Royal Society of Chemistry 2019-01-11 /pmc/articles/PMC9059666/ /pubmed/35518036 http://dx.doi.org/10.1039/c8ra10212k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Sobhani, Sara Chahkamali, Farhad Omarzehi Sansano, José Miguel A new bifunctional heterogeneous nanocatalyst for one-pot reduction-Schiff base condensation and reduction–carbonylation of nitroarenes |
title | A new bifunctional heterogeneous nanocatalyst for one-pot reduction-Schiff base condensation and reduction–carbonylation of nitroarenes |
title_full | A new bifunctional heterogeneous nanocatalyst for one-pot reduction-Schiff base condensation and reduction–carbonylation of nitroarenes |
title_fullStr | A new bifunctional heterogeneous nanocatalyst for one-pot reduction-Schiff base condensation and reduction–carbonylation of nitroarenes |
title_full_unstemmed | A new bifunctional heterogeneous nanocatalyst for one-pot reduction-Schiff base condensation and reduction–carbonylation of nitroarenes |
title_short | A new bifunctional heterogeneous nanocatalyst for one-pot reduction-Schiff base condensation and reduction–carbonylation of nitroarenes |
title_sort | new bifunctional heterogeneous nanocatalyst for one-pot reduction-schiff base condensation and reduction–carbonylation of nitroarenes |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059666/ https://www.ncbi.nlm.nih.gov/pubmed/35518036 http://dx.doi.org/10.1039/c8ra10212k |
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