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Reactivity of Aryl Halides for Reductive Dehalogenation in (Sea)water Using Polymer-Supported Terpyridine Palladium Catalyst
A polymer-supported terpyridine palladium complex was prepared. The complex was found to promote hydrodechlorination of aryl chlorides with potassium formate in seawater. Generally, reductive cleavage of aryl chlorides using transition metal catalysts is more difficult than that of aryl bromides and...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272388/ https://www.ncbi.nlm.nih.gov/pubmed/26029859 http://dx.doi.org/10.3390/molecules20069906 |
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author | Suzuka, Toshimasa Sueyoshi, Hiromu Maehara, Shohei Ogasawara, Hiroaki |
author_facet | Suzuka, Toshimasa Sueyoshi, Hiromu Maehara, Shohei Ogasawara, Hiroaki |
author_sort | Suzuka, Toshimasa |
collection | PubMed |
description | A polymer-supported terpyridine palladium complex was prepared. The complex was found to promote hydrodechlorination of aryl chlorides with potassium formate in seawater. Generally, reductive cleavage of aryl chlorides using transition metal catalysts is more difficult than that of aryl bromides and iodides (reactivity: I > Br > Cl); however, the results obtained did not follow the general trend. Therefore, we investigated the reaction inhibition agents and found a method to remove these inhibitors. The polymeric catalysts showed high catalytic activity and high reusability for transfer reduction in seawater. |
format | Online Article Text |
id | pubmed-6272388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62723882018-12-31 Reactivity of Aryl Halides for Reductive Dehalogenation in (Sea)water Using Polymer-Supported Terpyridine Palladium Catalyst Suzuka, Toshimasa Sueyoshi, Hiromu Maehara, Shohei Ogasawara, Hiroaki Molecules Communication A polymer-supported terpyridine palladium complex was prepared. The complex was found to promote hydrodechlorination of aryl chlorides with potassium formate in seawater. Generally, reductive cleavage of aryl chlorides using transition metal catalysts is more difficult than that of aryl bromides and iodides (reactivity: I > Br > Cl); however, the results obtained did not follow the general trend. Therefore, we investigated the reaction inhibition agents and found a method to remove these inhibitors. The polymeric catalysts showed high catalytic activity and high reusability for transfer reduction in seawater. MDPI 2015-05-28 /pmc/articles/PMC6272388/ /pubmed/26029859 http://dx.doi.org/10.3390/molecules20069906 Text en © 2015 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/4.0/). |
spellingShingle | Communication Suzuka, Toshimasa Sueyoshi, Hiromu Maehara, Shohei Ogasawara, Hiroaki Reactivity of Aryl Halides for Reductive Dehalogenation in (Sea)water Using Polymer-Supported Terpyridine Palladium Catalyst |
title | Reactivity of Aryl Halides for Reductive Dehalogenation in (Sea)water Using Polymer-Supported Terpyridine Palladium Catalyst |
title_full | Reactivity of Aryl Halides for Reductive Dehalogenation in (Sea)water Using Polymer-Supported Terpyridine Palladium Catalyst |
title_fullStr | Reactivity of Aryl Halides for Reductive Dehalogenation in (Sea)water Using Polymer-Supported Terpyridine Palladium Catalyst |
title_full_unstemmed | Reactivity of Aryl Halides for Reductive Dehalogenation in (Sea)water Using Polymer-Supported Terpyridine Palladium Catalyst |
title_short | Reactivity of Aryl Halides for Reductive Dehalogenation in (Sea)water Using Polymer-Supported Terpyridine Palladium Catalyst |
title_sort | reactivity of aryl halides for reductive dehalogenation in (sea)water using polymer-supported terpyridine palladium catalyst |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272388/ https://www.ncbi.nlm.nih.gov/pubmed/26029859 http://dx.doi.org/10.3390/molecules20069906 |
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