Cargando…
Modifying electron injection kinetics for selective photoreduction of nitroarenes into cyclic and asymmetric azo compounds
Modifying the reactivity of substrates by encapsulation is essential for microenvironment catalysts. Herein, we report an alternative strategy that modifies the entry behaviour of reactants into the microenvironment and substrate inclusion thermodynamics related to the capsule to control the electro...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9001638/ https://www.ncbi.nlm.nih.gov/pubmed/35410425 http://dx.doi.org/10.1038/s41467-022-29559-z |
_version_ | 1784685717936406528 |
---|---|
author | Yang, Yang Jing, Xu Zhang, Jing Yang, Fengyu Duan, Chunying |
author_facet | Yang, Yang Jing, Xu Zhang, Jing Yang, Fengyu Duan, Chunying |
author_sort | Yang, Yang |
collection | PubMed |
description | Modifying the reactivity of substrates by encapsulation is essential for microenvironment catalysts. Herein, we report an alternative strategy that modifies the entry behaviour of reactants into the microenvironment and substrate inclusion thermodynamics related to the capsule to control the electron injection kinetics and the selectivity of products from the nitroarenes photoreduction. The strategy includes the orchestration of capsule openings to control the electron injection kinetics of electron donors, and the capsule’s pocket to encapsulate more than one nitroarene molecules, facilitating a condensation reaction between the in situ formed azanol and nitroso species to produce azo product. The conceptual microenvironment catalyst endows selective conversion of asymmetric azo products from different nitroarenes, wherein, the estimated diameter and inclusion Gibbs free energy of substrates are used to control and predict the selectivity of products. Inhibition experiments confirm a typical enzymatic conversion, paving a new avenue for rational design of photocatalysts toward green chemistry. |
format | Online Article Text |
id | pubmed-9001638 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90016382022-04-27 Modifying electron injection kinetics for selective photoreduction of nitroarenes into cyclic and asymmetric azo compounds Yang, Yang Jing, Xu Zhang, Jing Yang, Fengyu Duan, Chunying Nat Commun Article Modifying the reactivity of substrates by encapsulation is essential for microenvironment catalysts. Herein, we report an alternative strategy that modifies the entry behaviour of reactants into the microenvironment and substrate inclusion thermodynamics related to the capsule to control the electron injection kinetics and the selectivity of products from the nitroarenes photoreduction. The strategy includes the orchestration of capsule openings to control the electron injection kinetics of electron donors, and the capsule’s pocket to encapsulate more than one nitroarene molecules, facilitating a condensation reaction between the in situ formed azanol and nitroso species to produce azo product. The conceptual microenvironment catalyst endows selective conversion of asymmetric azo products from different nitroarenes, wherein, the estimated diameter and inclusion Gibbs free energy of substrates are used to control and predict the selectivity of products. Inhibition experiments confirm a typical enzymatic conversion, paving a new avenue for rational design of photocatalysts toward green chemistry. Nature Publishing Group UK 2022-04-11 /pmc/articles/PMC9001638/ /pubmed/35410425 http://dx.doi.org/10.1038/s41467-022-29559-z 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 Yang, Yang Jing, Xu Zhang, Jing Yang, Fengyu Duan, Chunying Modifying electron injection kinetics for selective photoreduction of nitroarenes into cyclic and asymmetric azo compounds |
title | Modifying electron injection kinetics for selective photoreduction of nitroarenes into cyclic and asymmetric azo compounds |
title_full | Modifying electron injection kinetics for selective photoreduction of nitroarenes into cyclic and asymmetric azo compounds |
title_fullStr | Modifying electron injection kinetics for selective photoreduction of nitroarenes into cyclic and asymmetric azo compounds |
title_full_unstemmed | Modifying electron injection kinetics for selective photoreduction of nitroarenes into cyclic and asymmetric azo compounds |
title_short | Modifying electron injection kinetics for selective photoreduction of nitroarenes into cyclic and asymmetric azo compounds |
title_sort | modifying electron injection kinetics for selective photoreduction of nitroarenes into cyclic and asymmetric azo compounds |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9001638/ https://www.ncbi.nlm.nih.gov/pubmed/35410425 http://dx.doi.org/10.1038/s41467-022-29559-z |
work_keys_str_mv | AT yangyang modifyingelectroninjectionkineticsforselectivephotoreductionofnitroarenesintocyclicandasymmetricazocompounds AT jingxu modifyingelectroninjectionkineticsforselectivephotoreductionofnitroarenesintocyclicandasymmetricazocompounds AT zhangjing modifyingelectroninjectionkineticsforselectivephotoreductionofnitroarenesintocyclicandasymmetricazocompounds AT yangfengyu modifyingelectroninjectionkineticsforselectivephotoreductionofnitroarenesintocyclicandasymmetricazocompounds AT duanchunying modifyingelectroninjectionkineticsforselectivephotoreductionofnitroarenesintocyclicandasymmetricazocompounds |