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Catalytic nitrogen fixation using visible light energy
The synthesis of ammonia from atmospheric dinitrogen, nitrogen fixation, is one of the essential reactions for human beings. Because the current industrial nitrogen fixation depends on dihydrogen produced from fossil fuels as raw material, the development of a nitrogen fixation reaction that relies...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9715552/ https://www.ncbi.nlm.nih.gov/pubmed/36456553 http://dx.doi.org/10.1038/s41467-022-34984-1 |
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author | Ashida, Yuya Onozuka, Yuto Arashiba, Kazuya Konomi, Asuka Tanaka, Hiromasa Kuriyama, Shogo Yamazaki, Yasuomi Yoshizawa, Kazunari Nishibayashi, Yoshiaki |
author_facet | Ashida, Yuya Onozuka, Yuto Arashiba, Kazuya Konomi, Asuka Tanaka, Hiromasa Kuriyama, Shogo Yamazaki, Yasuomi Yoshizawa, Kazunari Nishibayashi, Yoshiaki |
author_sort | Ashida, Yuya |
collection | PubMed |
description | The synthesis of ammonia from atmospheric dinitrogen, nitrogen fixation, is one of the essential reactions for human beings. Because the current industrial nitrogen fixation depends on dihydrogen produced from fossil fuels as raw material, the development of a nitrogen fixation reaction that relies on the energy provided by renewable energy, such as visible light, is an important research goal from the viewpoint of sustainable chemistry. Herein, we establish an iridium- and molybdenum-catalysed process for synthesizing ammonia from dinitrogen under ambient reaction conditions and visible light irradiation. In this reaction system, iridium complexes and molybdenum triiodide complexes bearing N-heterocyclic carbene-based pincer ligands act as cooperative catalysts to activate 9,10-dihydroacridine and dinitrogen, respectively. The reaction of dinitrogen with 9,10-dihydroacridine is not thermodynamically favoured, and it only takes place under visible light irradiation. Therefore, the described reaction system is one that affords visible light energy–driven ammonia formation from dinitrogen catalytically. |
format | Online Article Text |
id | pubmed-9715552 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97155522022-12-03 Catalytic nitrogen fixation using visible light energy Ashida, Yuya Onozuka, Yuto Arashiba, Kazuya Konomi, Asuka Tanaka, Hiromasa Kuriyama, Shogo Yamazaki, Yasuomi Yoshizawa, Kazunari Nishibayashi, Yoshiaki Nat Commun Article The synthesis of ammonia from atmospheric dinitrogen, nitrogen fixation, is one of the essential reactions for human beings. Because the current industrial nitrogen fixation depends on dihydrogen produced from fossil fuels as raw material, the development of a nitrogen fixation reaction that relies on the energy provided by renewable energy, such as visible light, is an important research goal from the viewpoint of sustainable chemistry. Herein, we establish an iridium- and molybdenum-catalysed process for synthesizing ammonia from dinitrogen under ambient reaction conditions and visible light irradiation. In this reaction system, iridium complexes and molybdenum triiodide complexes bearing N-heterocyclic carbene-based pincer ligands act as cooperative catalysts to activate 9,10-dihydroacridine and dinitrogen, respectively. The reaction of dinitrogen with 9,10-dihydroacridine is not thermodynamically favoured, and it only takes place under visible light irradiation. Therefore, the described reaction system is one that affords visible light energy–driven ammonia formation from dinitrogen catalytically. Nature Publishing Group UK 2022-12-01 /pmc/articles/PMC9715552/ /pubmed/36456553 http://dx.doi.org/10.1038/s41467-022-34984-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ashida, Yuya Onozuka, Yuto Arashiba, Kazuya Konomi, Asuka Tanaka, Hiromasa Kuriyama, Shogo Yamazaki, Yasuomi Yoshizawa, Kazunari Nishibayashi, Yoshiaki Catalytic nitrogen fixation using visible light energy |
title | Catalytic nitrogen fixation using visible light energy |
title_full | Catalytic nitrogen fixation using visible light energy |
title_fullStr | Catalytic nitrogen fixation using visible light energy |
title_full_unstemmed | Catalytic nitrogen fixation using visible light energy |
title_short | Catalytic nitrogen fixation using visible light energy |
title_sort | catalytic nitrogen fixation using visible light energy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9715552/ https://www.ncbi.nlm.nih.gov/pubmed/36456553 http://dx.doi.org/10.1038/s41467-022-34984-1 |
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