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Recent Advances in the Synthesis of Aromatic Azo Compounds
Aromatic azo compounds have -N=N- double bonds as well as a larger π electron conjugation system, which endows aromatic azo compounds with wide applications in the fields of functional materials. The properties of aromatic azo compounds are closely related to the substituents on their aromatic rings...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10538219/ https://www.ncbi.nlm.nih.gov/pubmed/37764517 http://dx.doi.org/10.3390/molecules28186741 |
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author | Zhao, Meng-Yun Tang, Yue-Feng Han, Guo-Zhi |
author_facet | Zhao, Meng-Yun Tang, Yue-Feng Han, Guo-Zhi |
author_sort | Zhao, Meng-Yun |
collection | PubMed |
description | Aromatic azo compounds have -N=N- double bonds as well as a larger π electron conjugation system, which endows aromatic azo compounds with wide applications in the fields of functional materials. The properties of aromatic azo compounds are closely related to the substituents on their aromatic rings. However, traditional synthesis methods, such as the coupling of diazo salts, have a significant limitation with respect to the structural design of aromatic azo compounds. Therefore, many scientists have devoted their efforts to developing new synthetic methods. Moreover, recent advances in the synthesis of aromatic azo compounds have led to improvements in the design and preparation of light-response materials at the molecular level. This review summarizes the important synthetic progress of aromatic azo compounds in recent years, with an emphasis on the pioneering contribution of functional nanomaterials to the field. |
format | Online Article Text |
id | pubmed-10538219 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105382192023-09-29 Recent Advances in the Synthesis of Aromatic Azo Compounds Zhao, Meng-Yun Tang, Yue-Feng Han, Guo-Zhi Molecules Review Aromatic azo compounds have -N=N- double bonds as well as a larger π electron conjugation system, which endows aromatic azo compounds with wide applications in the fields of functional materials. The properties of aromatic azo compounds are closely related to the substituents on their aromatic rings. However, traditional synthesis methods, such as the coupling of diazo salts, have a significant limitation with respect to the structural design of aromatic azo compounds. Therefore, many scientists have devoted their efforts to developing new synthetic methods. Moreover, recent advances in the synthesis of aromatic azo compounds have led to improvements in the design and preparation of light-response materials at the molecular level. This review summarizes the important synthetic progress of aromatic azo compounds in recent years, with an emphasis on the pioneering contribution of functional nanomaterials to the field. MDPI 2023-09-21 /pmc/articles/PMC10538219/ /pubmed/37764517 http://dx.doi.org/10.3390/molecules28186741 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Zhao, Meng-Yun Tang, Yue-Feng Han, Guo-Zhi Recent Advances in the Synthesis of Aromatic Azo Compounds |
title | Recent Advances in the Synthesis of Aromatic Azo Compounds |
title_full | Recent Advances in the Synthesis of Aromatic Azo Compounds |
title_fullStr | Recent Advances in the Synthesis of Aromatic Azo Compounds |
title_full_unstemmed | Recent Advances in the Synthesis of Aromatic Azo Compounds |
title_short | Recent Advances in the Synthesis of Aromatic Azo Compounds |
title_sort | recent advances in the synthesis of aromatic azo compounds |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10538219/ https://www.ncbi.nlm.nih.gov/pubmed/37764517 http://dx.doi.org/10.3390/molecules28186741 |
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