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One-Pot Synthesis of Polypyrazoles by Click Reactions

We developed an efficient one-pot metal-free click polymerization procedure for the synthesis of 3,5-disubstituted polypyrazoles with high yields, high molecular weights, and narrow molecular weight distribution. The method involved two click reactions in a one-pot synthesis. The first reaction was...

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Detalles Bibliográficos
Autores principales: Wang, Shasha, Cheng, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5629195/
https://www.ncbi.nlm.nih.gov/pubmed/28983109
http://dx.doi.org/10.1038/s41598-017-12727-3
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author Wang, Shasha
Cheng, Bin
author_facet Wang, Shasha
Cheng, Bin
author_sort Wang, Shasha
collection PubMed
description We developed an efficient one-pot metal-free click polymerization procedure for the synthesis of 3,5-disubstituted polypyrazoles with high yields, high molecular weights, and narrow molecular weight distribution. The method involved two click reactions in a one-pot synthesis. The first reaction was the carbonyl chemistry of “non-aldol” type (condensation reaction of aldehydes with p-toluenesulfonylhydrazide), and the second was a click polymerization reaction of diazo compounds with alkynes. The reactions occurred sequentially by adding the reactants step by step. The diazo compound needed for the second click reaction was generated in situ by the first click reaction. The structures of the polypyrazoles were characterized by IR and (1)H NMR analyses. And their thermal properties and solubility were also tested.
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spelling pubmed-56291952017-10-13 One-Pot Synthesis of Polypyrazoles by Click Reactions Wang, Shasha Cheng, Bin Sci Rep Article We developed an efficient one-pot metal-free click polymerization procedure for the synthesis of 3,5-disubstituted polypyrazoles with high yields, high molecular weights, and narrow molecular weight distribution. The method involved two click reactions in a one-pot synthesis. The first reaction was the carbonyl chemistry of “non-aldol” type (condensation reaction of aldehydes with p-toluenesulfonylhydrazide), and the second was a click polymerization reaction of diazo compounds with alkynes. The reactions occurred sequentially by adding the reactants step by step. The diazo compound needed for the second click reaction was generated in situ by the first click reaction. The structures of the polypyrazoles were characterized by IR and (1)H NMR analyses. And their thermal properties and solubility were also tested. Nature Publishing Group UK 2017-10-05 /pmc/articles/PMC5629195/ /pubmed/28983109 http://dx.doi.org/10.1038/s41598-017-12727-3 Text en © The Author(s) 2017 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/.
spellingShingle Article
Wang, Shasha
Cheng, Bin
One-Pot Synthesis of Polypyrazoles by Click Reactions
title One-Pot Synthesis of Polypyrazoles by Click Reactions
title_full One-Pot Synthesis of Polypyrazoles by Click Reactions
title_fullStr One-Pot Synthesis of Polypyrazoles by Click Reactions
title_full_unstemmed One-Pot Synthesis of Polypyrazoles by Click Reactions
title_short One-Pot Synthesis of Polypyrazoles by Click Reactions
title_sort one-pot synthesis of polypyrazoles by click reactions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5629195/
https://www.ncbi.nlm.nih.gov/pubmed/28983109
http://dx.doi.org/10.1038/s41598-017-12727-3
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