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Chiral Pt/ZrO(2 )Catalysts. Enantioselective Hydrogenation of 1-phenyl-1,2-propanedione
The enantioselective hydrogenation of 1-phenyl-1,2-propanedione over Pt colloids stabilized with (R,S)-4,5-dihydro-4,5-diphenyl-2-(6-cyanopyridinyl)imidazoline (CI) supported on a meso-structured ZrO(2) under a pressure of 40 bar of H(2) at 298 K has been investigated(.) The metal loading in all cat...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263364/ https://www.ncbi.nlm.nih.gov/pubmed/20657492 http://dx.doi.org/10.3390/molecules15053428 |
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author | Urbina, Claudia Campos, Cristian Pecchi, Gina Claver, Carmen Reyes, Patricio |
author_facet | Urbina, Claudia Campos, Cristian Pecchi, Gina Claver, Carmen Reyes, Patricio |
author_sort | Urbina, Claudia |
collection | PubMed |
description | The enantioselective hydrogenation of 1-phenyl-1,2-propanedione over Pt colloids stabilized with (R,S)-4,5-dihydro-4,5-diphenyl-2-(6-cyanopyridinyl)imidazoline (CI) supported on a meso-structured ZrO(2) under a pressure of 40 bar of H(2) at 298 K has been investigated(.) The metal loading in all catalysts was 1 wt%. The effect of the amount of chiral modifier on the metal particle size and on the catalytic behavior was analyzed. It was found that as the CI/Pt molar ratio increases from 2.5 to 3.5 the Pt crystal size decreases from 3.0 to 1.8 nm. All catalysts were very active in the studied reaction, with the most active one being the catalyst with smaller Pt particles, whereas the selectivity is higher in those catalysts with larger chiral modified Pt metal particles. |
format | Online Article Text |
id | pubmed-6263364 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62633642019-01-02 Chiral Pt/ZrO(2 )Catalysts. Enantioselective Hydrogenation of 1-phenyl-1,2-propanedione Urbina, Claudia Campos, Cristian Pecchi, Gina Claver, Carmen Reyes, Patricio Molecules Article The enantioselective hydrogenation of 1-phenyl-1,2-propanedione over Pt colloids stabilized with (R,S)-4,5-dihydro-4,5-diphenyl-2-(6-cyanopyridinyl)imidazoline (CI) supported on a meso-structured ZrO(2) under a pressure of 40 bar of H(2) at 298 K has been investigated(.) The metal loading in all catalysts was 1 wt%. The effect of the amount of chiral modifier on the metal particle size and on the catalytic behavior was analyzed. It was found that as the CI/Pt molar ratio increases from 2.5 to 3.5 the Pt crystal size decreases from 3.0 to 1.8 nm. All catalysts were very active in the studied reaction, with the most active one being the catalyst with smaller Pt particles, whereas the selectivity is higher in those catalysts with larger chiral modified Pt metal particles. MDPI 2010-05-12 /pmc/articles/PMC6263364/ /pubmed/20657492 http://dx.doi.org/10.3390/molecules15053428 Text en © 2010 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 license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Urbina, Claudia Campos, Cristian Pecchi, Gina Claver, Carmen Reyes, Patricio Chiral Pt/ZrO(2 )Catalysts. Enantioselective Hydrogenation of 1-phenyl-1,2-propanedione |
title | Chiral Pt/ZrO(2 )Catalysts. Enantioselective Hydrogenation of 1-phenyl-1,2-propanedione |
title_full | Chiral Pt/ZrO(2 )Catalysts. Enantioselective Hydrogenation of 1-phenyl-1,2-propanedione |
title_fullStr | Chiral Pt/ZrO(2 )Catalysts. Enantioselective Hydrogenation of 1-phenyl-1,2-propanedione |
title_full_unstemmed | Chiral Pt/ZrO(2 )Catalysts. Enantioselective Hydrogenation of 1-phenyl-1,2-propanedione |
title_short | Chiral Pt/ZrO(2 )Catalysts. Enantioselective Hydrogenation of 1-phenyl-1,2-propanedione |
title_sort | chiral pt/zro(2 )catalysts. enantioselective hydrogenation of 1-phenyl-1,2-propanedione |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263364/ https://www.ncbi.nlm.nih.gov/pubmed/20657492 http://dx.doi.org/10.3390/molecules15053428 |
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