Cargando…
A Recyclable Cu-MOF-74 Catalyst for the Ligand-Free O-Arylation Reaction of 4-Nitrobenzaldehyde and Phenol
The activity and recyclability of Cu-MOF-74 as a catalyst was studied for the ligand-free C–O cross-coupling reaction of 4-nitrobenzaldehyde (NB) with phenol (Ph) to form 4-formyldiphenyl ether (FDE). Cu-MOF-74 is characterized by having unsaturated copper sites in a highly porous metal-organic fram...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485796/ https://www.ncbi.nlm.nih.gov/pubmed/28621710 http://dx.doi.org/10.3390/nano7060149 |
_version_ | 1783246144730562560 |
---|---|
author | Leo, Pedro Orcajo, Gisela Briones, David Calleja, Guillermo Sánchez-Sánchez, Manuel Martínez, Fernando |
author_facet | Leo, Pedro Orcajo, Gisela Briones, David Calleja, Guillermo Sánchez-Sánchez, Manuel Martínez, Fernando |
author_sort | Leo, Pedro |
collection | PubMed |
description | The activity and recyclability of Cu-MOF-74 as a catalyst was studied for the ligand-free C–O cross-coupling reaction of 4-nitrobenzaldehyde (NB) with phenol (Ph) to form 4-formyldiphenyl ether (FDE). Cu-MOF-74 is characterized by having unsaturated copper sites in a highly porous metal-organic framework. The influence of solvent, reaction temperature, NB/Ph ratio, catalyst concentration, and basic agent (type and concentration) were evaluated. High conversions were achieved at 120 °C, 5 mol % of catalyst, NB/Ph ratio of 1:2, DMF as solvent, and 1 equivalent of K(2)CO(3) base. The activity of Cu-MOF-74 material was higher than other ligand-free copper catalytic systems tested in this study. This catalyst was easily separated and reused in five successive runs, achieving a remarkable performance without significant porous framework degradation. The leaching of copper species in the reaction medium was negligible. The O-arylation between NB and Ph took place only in the presence of Cu-MOF-74 material, being negligible without the solid catalyst. The catalytic advantages of using nanostructured Cu-MOF-74 catalyst were also proven. |
format | Online Article Text |
id | pubmed-5485796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-54857962017-06-29 A Recyclable Cu-MOF-74 Catalyst for the Ligand-Free O-Arylation Reaction of 4-Nitrobenzaldehyde and Phenol Leo, Pedro Orcajo, Gisela Briones, David Calleja, Guillermo Sánchez-Sánchez, Manuel Martínez, Fernando Nanomaterials (Basel) Article The activity and recyclability of Cu-MOF-74 as a catalyst was studied for the ligand-free C–O cross-coupling reaction of 4-nitrobenzaldehyde (NB) with phenol (Ph) to form 4-formyldiphenyl ether (FDE). Cu-MOF-74 is characterized by having unsaturated copper sites in a highly porous metal-organic framework. The influence of solvent, reaction temperature, NB/Ph ratio, catalyst concentration, and basic agent (type and concentration) were evaluated. High conversions were achieved at 120 °C, 5 mol % of catalyst, NB/Ph ratio of 1:2, DMF as solvent, and 1 equivalent of K(2)CO(3) base. The activity of Cu-MOF-74 material was higher than other ligand-free copper catalytic systems tested in this study. This catalyst was easily separated and reused in five successive runs, achieving a remarkable performance without significant porous framework degradation. The leaching of copper species in the reaction medium was negligible. The O-arylation between NB and Ph took place only in the presence of Cu-MOF-74 material, being negligible without the solid catalyst. The catalytic advantages of using nanostructured Cu-MOF-74 catalyst were also proven. MDPI 2017-06-16 /pmc/articles/PMC5485796/ /pubmed/28621710 http://dx.doi.org/10.3390/nano7060149 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Leo, Pedro Orcajo, Gisela Briones, David Calleja, Guillermo Sánchez-Sánchez, Manuel Martínez, Fernando A Recyclable Cu-MOF-74 Catalyst for the Ligand-Free O-Arylation Reaction of 4-Nitrobenzaldehyde and Phenol |
title | A Recyclable Cu-MOF-74 Catalyst for the Ligand-Free O-Arylation Reaction of 4-Nitrobenzaldehyde and Phenol |
title_full | A Recyclable Cu-MOF-74 Catalyst for the Ligand-Free O-Arylation Reaction of 4-Nitrobenzaldehyde and Phenol |
title_fullStr | A Recyclable Cu-MOF-74 Catalyst for the Ligand-Free O-Arylation Reaction of 4-Nitrobenzaldehyde and Phenol |
title_full_unstemmed | A Recyclable Cu-MOF-74 Catalyst for the Ligand-Free O-Arylation Reaction of 4-Nitrobenzaldehyde and Phenol |
title_short | A Recyclable Cu-MOF-74 Catalyst for the Ligand-Free O-Arylation Reaction of 4-Nitrobenzaldehyde and Phenol |
title_sort | recyclable cu-mof-74 catalyst for the ligand-free o-arylation reaction of 4-nitrobenzaldehyde and phenol |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485796/ https://www.ncbi.nlm.nih.gov/pubmed/28621710 http://dx.doi.org/10.3390/nano7060149 |
work_keys_str_mv | AT leopedro arecyclablecumof74catalystfortheligandfreeoarylationreactionof4nitrobenzaldehydeandphenol AT orcajogisela arecyclablecumof74catalystfortheligandfreeoarylationreactionof4nitrobenzaldehydeandphenol AT brionesdavid arecyclablecumof74catalystfortheligandfreeoarylationreactionof4nitrobenzaldehydeandphenol AT callejaguillermo arecyclablecumof74catalystfortheligandfreeoarylationreactionof4nitrobenzaldehydeandphenol AT sanchezsanchezmanuel arecyclablecumof74catalystfortheligandfreeoarylationreactionof4nitrobenzaldehydeandphenol AT martinezfernando arecyclablecumof74catalystfortheligandfreeoarylationreactionof4nitrobenzaldehydeandphenol AT leopedro recyclablecumof74catalystfortheligandfreeoarylationreactionof4nitrobenzaldehydeandphenol AT orcajogisela recyclablecumof74catalystfortheligandfreeoarylationreactionof4nitrobenzaldehydeandphenol AT brionesdavid recyclablecumof74catalystfortheligandfreeoarylationreactionof4nitrobenzaldehydeandphenol AT callejaguillermo recyclablecumof74catalystfortheligandfreeoarylationreactionof4nitrobenzaldehydeandphenol AT sanchezsanchezmanuel recyclablecumof74catalystfortheligandfreeoarylationreactionof4nitrobenzaldehydeandphenol AT martinezfernando recyclablecumof74catalystfortheligandfreeoarylationreactionof4nitrobenzaldehydeandphenol |