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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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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. |
format | Online Article Text |
id | pubmed-5629195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT wangshasha onepotsynthesisofpolypyrazolesbyclickreactions AT chengbin onepotsynthesisofpolypyrazolesbyclickreactions |