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Protocol for microwave-assisted synthesis of unsymmetrical azo dyes
Aromatic azo dyes bear immense commercial significance because of their extensive usage in the textile, paint, and food industries. With growing environmental concerns, developing alternative greener approaches for the synthesis of azo dyes is crucial. Herein, we describe a metal-free, microwave (MW...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9678771/ https://www.ncbi.nlm.nih.gov/pubmed/36595940 http://dx.doi.org/10.1016/j.xpro.2022.101864 |
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author | Thakuri, Ankit Banerjee, Mainak Chatterjee, Amrita |
author_facet | Thakuri, Ankit Banerjee, Mainak Chatterjee, Amrita |
author_sort | Thakuri, Ankit |
collection | PubMed |
description | Aromatic azo dyes bear immense commercial significance because of their extensive usage in the textile, paint, and food industries. With growing environmental concerns, developing alternative greener approaches for the synthesis of azo dyes is crucial. Herein, we describe a metal-free, microwave (MW)-assisted protocol for rapid access to a large variety of unsymmetrical azo dyes by coupling nitroarenes and aromatic amines. After MW-assisted coupling, the azo dyes are then isolated by precipitation followed by recrystallization to obtain pure azo dyes. For complete details on the use and execution of this protocol, please refer to Thakuri et al. (2022).(1) |
format | Online Article Text |
id | pubmed-9678771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-96787712022-11-23 Protocol for microwave-assisted synthesis of unsymmetrical azo dyes Thakuri, Ankit Banerjee, Mainak Chatterjee, Amrita STAR Protoc Protocol Aromatic azo dyes bear immense commercial significance because of their extensive usage in the textile, paint, and food industries. With growing environmental concerns, developing alternative greener approaches for the synthesis of azo dyes is crucial. Herein, we describe a metal-free, microwave (MW)-assisted protocol for rapid access to a large variety of unsymmetrical azo dyes by coupling nitroarenes and aromatic amines. After MW-assisted coupling, the azo dyes are then isolated by precipitation followed by recrystallization to obtain pure azo dyes. For complete details on the use and execution of this protocol, please refer to Thakuri et al. (2022).(1) Elsevier 2022-11-17 /pmc/articles/PMC9678771/ /pubmed/36595940 http://dx.doi.org/10.1016/j.xpro.2022.101864 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Protocol Thakuri, Ankit Banerjee, Mainak Chatterjee, Amrita Protocol for microwave-assisted synthesis of unsymmetrical azo dyes |
title | Protocol for microwave-assisted synthesis of unsymmetrical azo dyes |
title_full | Protocol for microwave-assisted synthesis of unsymmetrical azo dyes |
title_fullStr | Protocol for microwave-assisted synthesis of unsymmetrical azo dyes |
title_full_unstemmed | Protocol for microwave-assisted synthesis of unsymmetrical azo dyes |
title_short | Protocol for microwave-assisted synthesis of unsymmetrical azo dyes |
title_sort | protocol for microwave-assisted synthesis of unsymmetrical azo dyes |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9678771/ https://www.ncbi.nlm.nih.gov/pubmed/36595940 http://dx.doi.org/10.1016/j.xpro.2022.101864 |
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