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Ru/UiO-66 Catalyst for the Reduction of Nitroarenes and Tandem Reaction of Alcohol Oxidation/Knoevenagel Condensation
[Image: see text] A 3.1% Ru/UiO-66 material was prepared by adsorption of RuCl(3) from ethyl acetate on to MOF UiO-66, followed by reduction with NaBH(4). The presence of acid–base and ox-red sites allows this 3.1% Ru/UiO-66 material acting as a bifunctional catalyst for the reduction of nitroarenes...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641650/ https://www.ncbi.nlm.nih.gov/pubmed/31458654 http://dx.doi.org/10.1021/acsomega.8b00157 |
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author | Yang, Qiming Zhang, Hong-Yu Wang, Liping Zhang, Yuecheng Zhao, Jiquan |
author_facet | Yang, Qiming Zhang, Hong-Yu Wang, Liping Zhang, Yuecheng Zhao, Jiquan |
author_sort | Yang, Qiming |
collection | PubMed |
description | [Image: see text] A 3.1% Ru/UiO-66 material was prepared by adsorption of RuCl(3) from ethyl acetate on to MOF UiO-66, followed by reduction with NaBH(4). The presence of acid–base and ox-red sites allows this 3.1% Ru/UiO-66 material acting as a bifunctional catalyst for the reduction of nitroarenes and tandem reaction of alcohol oxidation/Knoevenagel condensation. The high efficiency of 3.1% Ru/UiO-66 was demonstrated in the reduction of nitroarenes to amines. This system can be applied as a catalyst for at least six successive cycles without loss of activity. The 3.1% Ru/UiO-66 catalyst also was active in the tandem aerobic oxidation of alcohols/Knoevenagel condensation with malononitrile. However, the activity of this catalyst strongly decreased in the second cycle. A combination of physicochemical and catalytic experimental data indicated that Ru nanoparticles are the active sites both for the catalytic reduction of nitro compounds and the aerobic oxidation of alcohols. The activity for the Knoevenagel condensation reaction was from the existence of the “Zr(n+)–O(2–) Lewis acid–base” pair in the framework of UiO-66. |
format | Online Article Text |
id | pubmed-6641650 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66416502019-08-27 Ru/UiO-66 Catalyst for the Reduction of Nitroarenes and Tandem Reaction of Alcohol Oxidation/Knoevenagel Condensation Yang, Qiming Zhang, Hong-Yu Wang, Liping Zhang, Yuecheng Zhao, Jiquan ACS Omega [Image: see text] A 3.1% Ru/UiO-66 material was prepared by adsorption of RuCl(3) from ethyl acetate on to MOF UiO-66, followed by reduction with NaBH(4). The presence of acid–base and ox-red sites allows this 3.1% Ru/UiO-66 material acting as a bifunctional catalyst for the reduction of nitroarenes and tandem reaction of alcohol oxidation/Knoevenagel condensation. The high efficiency of 3.1% Ru/UiO-66 was demonstrated in the reduction of nitroarenes to amines. This system can be applied as a catalyst for at least six successive cycles without loss of activity. The 3.1% Ru/UiO-66 catalyst also was active in the tandem aerobic oxidation of alcohols/Knoevenagel condensation with malononitrile. However, the activity of this catalyst strongly decreased in the second cycle. A combination of physicochemical and catalytic experimental data indicated that Ru nanoparticles are the active sites both for the catalytic reduction of nitro compounds and the aerobic oxidation of alcohols. The activity for the Knoevenagel condensation reaction was from the existence of the “Zr(n+)–O(2–) Lewis acid–base” pair in the framework of UiO-66. American Chemical Society 2018-04-13 /pmc/articles/PMC6641650/ /pubmed/31458654 http://dx.doi.org/10.1021/acsomega.8b00157 Text en Copyright © 2018 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 | Yang, Qiming Zhang, Hong-Yu Wang, Liping Zhang, Yuecheng Zhao, Jiquan Ru/UiO-66 Catalyst for the Reduction of Nitroarenes and Tandem Reaction of Alcohol Oxidation/Knoevenagel Condensation |
title | Ru/UiO-66 Catalyst for the Reduction of Nitroarenes
and Tandem Reaction of Alcohol Oxidation/Knoevenagel Condensation |
title_full | Ru/UiO-66 Catalyst for the Reduction of Nitroarenes
and Tandem Reaction of Alcohol Oxidation/Knoevenagel Condensation |
title_fullStr | Ru/UiO-66 Catalyst for the Reduction of Nitroarenes
and Tandem Reaction of Alcohol Oxidation/Knoevenagel Condensation |
title_full_unstemmed | Ru/UiO-66 Catalyst for the Reduction of Nitroarenes
and Tandem Reaction of Alcohol Oxidation/Knoevenagel Condensation |
title_short | Ru/UiO-66 Catalyst for the Reduction of Nitroarenes
and Tandem Reaction of Alcohol Oxidation/Knoevenagel Condensation |
title_sort | ru/uio-66 catalyst for the reduction of nitroarenes
and tandem reaction of alcohol oxidation/knoevenagel condensation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641650/ https://www.ncbi.nlm.nih.gov/pubmed/31458654 http://dx.doi.org/10.1021/acsomega.8b00157 |
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