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Tandem utilization of CO(2) photoreduction products for the carbonylation of aryl iodides
Photocatalytic CO(2) reduction reaction has been developed as an effective strategy to convert CO(2) into reusable chemicals. However, the reduction products of this reaction are often of low utilization value. Herein, we effectively connect photocatalytic CO(2) reduction and amino carbonylation rea...
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/PMC9135707/ https://www.ncbi.nlm.nih.gov/pubmed/35618727 http://dx.doi.org/10.1038/s41467-022-30676-y |
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author | Xia, Yuan-Sheng Tang, Meizhong Zhang, Lei Liu, Jiang Jiang, Cheng Gao, Guang-Kuo Dong, Long-Zhang Xie, Lan-Gui Lan, Ya-Qian |
author_facet | Xia, Yuan-Sheng Tang, Meizhong Zhang, Lei Liu, Jiang Jiang, Cheng Gao, Guang-Kuo Dong, Long-Zhang Xie, Lan-Gui Lan, Ya-Qian |
author_sort | Xia, Yuan-Sheng |
collection | PubMed |
description | Photocatalytic CO(2) reduction reaction has been developed as an effective strategy to convert CO(2) into reusable chemicals. However, the reduction products of this reaction are often of low utilization value. Herein, we effectively connect photocatalytic CO(2) reduction and amino carbonylation reactions in series to reconvert inexpensive photoreduction product CO into value-added and easily isolated fine chemicals. In this tandem transformation system, we synthesize an efficient photocatalyst, NNU-55-Ni, which is transformed into nanosheets (NNU-55-Ni-NS) in situ to improve the photocatalytic CO(2)-to-CO activity significantly. After that, CO serving as reactant is further reconverted into organic molecules through the coupled carbonylation reactions. Especially in the carbonylation reaction of diethyltoluamide synthesis, CO conversion reaches up to 85%. Meanwhile, this tandem transformation also provides a simple and low-cost method for the (13)C isotopically labeled organic molecules. This work represents an important and feasible pathway for the subsequent separation and application of CO(2) photoreduction product. |
format | Online Article Text |
id | pubmed-9135707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91357072022-05-28 Tandem utilization of CO(2) photoreduction products for the carbonylation of aryl iodides Xia, Yuan-Sheng Tang, Meizhong Zhang, Lei Liu, Jiang Jiang, Cheng Gao, Guang-Kuo Dong, Long-Zhang Xie, Lan-Gui Lan, Ya-Qian Nat Commun Article Photocatalytic CO(2) reduction reaction has been developed as an effective strategy to convert CO(2) into reusable chemicals. However, the reduction products of this reaction are often of low utilization value. Herein, we effectively connect photocatalytic CO(2) reduction and amino carbonylation reactions in series to reconvert inexpensive photoreduction product CO into value-added and easily isolated fine chemicals. In this tandem transformation system, we synthesize an efficient photocatalyst, NNU-55-Ni, which is transformed into nanosheets (NNU-55-Ni-NS) in situ to improve the photocatalytic CO(2)-to-CO activity significantly. After that, CO serving as reactant is further reconverted into organic molecules through the coupled carbonylation reactions. Especially in the carbonylation reaction of diethyltoluamide synthesis, CO conversion reaches up to 85%. Meanwhile, this tandem transformation also provides a simple and low-cost method for the (13)C isotopically labeled organic molecules. This work represents an important and feasible pathway for the subsequent separation and application of CO(2) photoreduction product. Nature Publishing Group UK 2022-05-26 /pmc/articles/PMC9135707/ /pubmed/35618727 http://dx.doi.org/10.1038/s41467-022-30676-y 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 Xia, Yuan-Sheng Tang, Meizhong Zhang, Lei Liu, Jiang Jiang, Cheng Gao, Guang-Kuo Dong, Long-Zhang Xie, Lan-Gui Lan, Ya-Qian Tandem utilization of CO(2) photoreduction products for the carbonylation of aryl iodides |
title | Tandem utilization of CO(2) photoreduction products for the carbonylation of aryl iodides |
title_full | Tandem utilization of CO(2) photoreduction products for the carbonylation of aryl iodides |
title_fullStr | Tandem utilization of CO(2) photoreduction products for the carbonylation of aryl iodides |
title_full_unstemmed | Tandem utilization of CO(2) photoreduction products for the carbonylation of aryl iodides |
title_short | Tandem utilization of CO(2) photoreduction products for the carbonylation of aryl iodides |
title_sort | tandem utilization of co(2) photoreduction products for the carbonylation of aryl iodides |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9135707/ https://www.ncbi.nlm.nih.gov/pubmed/35618727 http://dx.doi.org/10.1038/s41467-022-30676-y |
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