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A Convenient and Stable Heterogeneous Nickel Catalyst for Hydrodehalogenation of Aryl Halides Using Molecular Hydrogen
Hydrodehalogenation is an effective strategy for transforming persistent and potentially toxic organohalides into their more benign congeners. Common methods utilize Pd/C or Raney‐nickel as catalysts, which are either expensive or have safety concerns. In this study, a nickel‐based catalyst supporte...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9306955/ https://www.ncbi.nlm.nih.gov/pubmed/34978382 http://dx.doi.org/10.1002/cssc.202102315 |
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author | Leonard, David K. Ryabchuk, Pavel Anwar, Muhammad Dastgir, Sarim Junge, Kathrin Beller, Matthias |
author_facet | Leonard, David K. Ryabchuk, Pavel Anwar, Muhammad Dastgir, Sarim Junge, Kathrin Beller, Matthias |
author_sort | Leonard, David K. |
collection | PubMed |
description | Hydrodehalogenation is an effective strategy for transforming persistent and potentially toxic organohalides into their more benign congeners. Common methods utilize Pd/C or Raney‐nickel as catalysts, which are either expensive or have safety concerns. In this study, a nickel‐based catalyst supported on titania (Ni‐phen@TiO(2)‐800) is used as a safe alternative to pyrophoric Raney‐nickel. The catalyst is prepared in a straightforward fashion by deposition of nickel(II)/1,10‐phenanthroline on titania, followed by pyrolysis. The catalytic material, which was characterized by SEM, TEM, XRD, and XPS, consists of nickel nanoparticles covered with N‐doped carbon layers. By using design of experiments (DoE), this nanostructured catalyst is found to be proficient for the facile and selective hydrodehalogenation of a diverse range of substrates bearing C−I, C−Br, or C−Cl bonds (>30 examples). The practicality of this catalyst system is demonstrated by the dehalogenation of environmentally hazardous and polyhalogenated substrates atrazine, tetrabromobisphenol A, tetrachlorobenzene, and a polybrominated diphenyl ether (PBDE). |
format | Online Article Text |
id | pubmed-9306955 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93069552022-07-28 A Convenient and Stable Heterogeneous Nickel Catalyst for Hydrodehalogenation of Aryl Halides Using Molecular Hydrogen Leonard, David K. Ryabchuk, Pavel Anwar, Muhammad Dastgir, Sarim Junge, Kathrin Beller, Matthias ChemSusChem Research Articles Hydrodehalogenation is an effective strategy for transforming persistent and potentially toxic organohalides into their more benign congeners. Common methods utilize Pd/C or Raney‐nickel as catalysts, which are either expensive or have safety concerns. In this study, a nickel‐based catalyst supported on titania (Ni‐phen@TiO(2)‐800) is used as a safe alternative to pyrophoric Raney‐nickel. The catalyst is prepared in a straightforward fashion by deposition of nickel(II)/1,10‐phenanthroline on titania, followed by pyrolysis. The catalytic material, which was characterized by SEM, TEM, XRD, and XPS, consists of nickel nanoparticles covered with N‐doped carbon layers. By using design of experiments (DoE), this nanostructured catalyst is found to be proficient for the facile and selective hydrodehalogenation of a diverse range of substrates bearing C−I, C−Br, or C−Cl bonds (>30 examples). The practicality of this catalyst system is demonstrated by the dehalogenation of environmentally hazardous and polyhalogenated substrates atrazine, tetrabromobisphenol A, tetrachlorobenzene, and a polybrominated diphenyl ether (PBDE). John Wiley and Sons Inc. 2022-01-27 2022-03-08 /pmc/articles/PMC9306955/ /pubmed/34978382 http://dx.doi.org/10.1002/cssc.202102315 Text en © 2022 The Authors. ChemSusChem published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles Leonard, David K. Ryabchuk, Pavel Anwar, Muhammad Dastgir, Sarim Junge, Kathrin Beller, Matthias A Convenient and Stable Heterogeneous Nickel Catalyst for Hydrodehalogenation of Aryl Halides Using Molecular Hydrogen |
title | A Convenient and Stable Heterogeneous Nickel Catalyst for Hydrodehalogenation of Aryl Halides Using Molecular Hydrogen |
title_full | A Convenient and Stable Heterogeneous Nickel Catalyst for Hydrodehalogenation of Aryl Halides Using Molecular Hydrogen |
title_fullStr | A Convenient and Stable Heterogeneous Nickel Catalyst for Hydrodehalogenation of Aryl Halides Using Molecular Hydrogen |
title_full_unstemmed | A Convenient and Stable Heterogeneous Nickel Catalyst for Hydrodehalogenation of Aryl Halides Using Molecular Hydrogen |
title_short | A Convenient and Stable Heterogeneous Nickel Catalyst for Hydrodehalogenation of Aryl Halides Using Molecular Hydrogen |
title_sort | convenient and stable heterogeneous nickel catalyst for hydrodehalogenation of aryl halides using molecular hydrogen |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9306955/ https://www.ncbi.nlm.nih.gov/pubmed/34978382 http://dx.doi.org/10.1002/cssc.202102315 |
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