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Iodine‐Catalysed Dissolution of Elemental Gold in Ethanol
Gold is a scarce element in the Earth's crust but indispensable in modern electronic devices. New, sustainable methods of gold recycling are essential to meet the growing eco‐social demand of gold. Here, we describe a simple, inexpensive, and environmentally benign dissolution of gold under mil...
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/PMC9305299/ https://www.ncbi.nlm.nih.gov/pubmed/35106899 http://dx.doi.org/10.1002/anie.202117587 |
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author | Zupanc, Anže Heliövaara, Eeva Moslova, Karina Eronen, Aleksi Kemell, Marianna Podlipnik, Črtomir Jereb, Marjan Repo, Timo |
author_facet | Zupanc, Anže Heliövaara, Eeva Moslova, Karina Eronen, Aleksi Kemell, Marianna Podlipnik, Črtomir Jereb, Marjan Repo, Timo |
author_sort | Zupanc, Anže |
collection | PubMed |
description | Gold is a scarce element in the Earth's crust but indispensable in modern electronic devices. New, sustainable methods of gold recycling are essential to meet the growing eco‐social demand of gold. Here, we describe a simple, inexpensive, and environmentally benign dissolution of gold under mild conditions. Gold dissolves quantitatively in ethanol using 2‐mercaptobenzimidazole as a ligand in the presence of a catalytic amount of iodine. Mechanistically, the dissolution of gold begins when I(2) oxidizes Au(0) and forms a [Au(I)I(2)](−) species, which undergoes subsequent ligand‐exchange reactions and forms a stable bis‐ligand Au(I) complex. H(2)O(2) oxidizes free iodide and regenerated I(2) returns back to the catalytic cycle. Addition of a reductant to the reaction mixture precipitates gold quantitatively and partially regenerates the ligand. We anticipate our work will open a new pathway to more sustainable metal recycling with the utilization of just catalytic amounts of reagents and green solvents. |
format | Online Article Text |
id | pubmed-9305299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93052992022-07-28 Iodine‐Catalysed Dissolution of Elemental Gold in Ethanol Zupanc, Anže Heliövaara, Eeva Moslova, Karina Eronen, Aleksi Kemell, Marianna Podlipnik, Črtomir Jereb, Marjan Repo, Timo Angew Chem Int Ed Engl Research Articles Gold is a scarce element in the Earth's crust but indispensable in modern electronic devices. New, sustainable methods of gold recycling are essential to meet the growing eco‐social demand of gold. Here, we describe a simple, inexpensive, and environmentally benign dissolution of gold under mild conditions. Gold dissolves quantitatively in ethanol using 2‐mercaptobenzimidazole as a ligand in the presence of a catalytic amount of iodine. Mechanistically, the dissolution of gold begins when I(2) oxidizes Au(0) and forms a [Au(I)I(2)](−) species, which undergoes subsequent ligand‐exchange reactions and forms a stable bis‐ligand Au(I) complex. H(2)O(2) oxidizes free iodide and regenerated I(2) returns back to the catalytic cycle. Addition of a reductant to the reaction mixture precipitates gold quantitatively and partially regenerates the ligand. We anticipate our work will open a new pathway to more sustainable metal recycling with the utilization of just catalytic amounts of reagents and green solvents. John Wiley and Sons Inc. 2022-02-15 2022-03-28 /pmc/articles/PMC9305299/ /pubmed/35106899 http://dx.doi.org/10.1002/anie.202117587 Text en © 2022 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Zupanc, Anže Heliövaara, Eeva Moslova, Karina Eronen, Aleksi Kemell, Marianna Podlipnik, Črtomir Jereb, Marjan Repo, Timo Iodine‐Catalysed Dissolution of Elemental Gold in Ethanol |
title | Iodine‐Catalysed Dissolution of Elemental Gold in Ethanol |
title_full | Iodine‐Catalysed Dissolution of Elemental Gold in Ethanol |
title_fullStr | Iodine‐Catalysed Dissolution of Elemental Gold in Ethanol |
title_full_unstemmed | Iodine‐Catalysed Dissolution of Elemental Gold in Ethanol |
title_short | Iodine‐Catalysed Dissolution of Elemental Gold in Ethanol |
title_sort | iodine‐catalysed dissolution of elemental gold in ethanol |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9305299/ https://www.ncbi.nlm.nih.gov/pubmed/35106899 http://dx.doi.org/10.1002/anie.202117587 |
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