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Synthesis of Polyfluorinated Thia- and Oxathiacalixarenes Based on Perfluoro-m-xylene
Perfluorinated tetrathiacalix[4]arene was obtained by heating perfluoro-m-xylene with thiourea or 2,5-difluoro-4,6-bis(trifluoromethyl)benzene-1,3-dithiol at 90 °C. Interaction of perfluoro-m-xylene with resorcinol or orcinol under mild conditions and subsequent heating of the mixture with 2,5-diflu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864041/ https://www.ncbi.nlm.nih.gov/pubmed/33498335 http://dx.doi.org/10.3390/molecules26030526 |
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author | Kovtonyuk, Vladimir N. Gatilov, Yuri V. Nikul’shin, Pavel V. Bredikhin, Roman A. |
author_facet | Kovtonyuk, Vladimir N. Gatilov, Yuri V. Nikul’shin, Pavel V. Bredikhin, Roman A. |
author_sort | Kovtonyuk, Vladimir N. |
collection | PubMed |
description | Perfluorinated tetrathiacalix[4]arene was obtained by heating perfluoro-m-xylene with thiourea or 2,5-difluoro-4,6-bis(trifluoromethyl)benzene-1,3-dithiol at 90 °C. Interaction of perfluoro-m-xylene with resorcinol or orcinol under mild conditions and subsequent heating of the mixture with 2,5-difluoro-4,6-bis(trifluoromethyl)benzene-1,3-dithiol leads to polyfluorinated dioxadithiacalix[4]arenes. Triphenyl and pentaphenyl ethers formed by the interaction of perfluoro-m-xylene with resorcinol under heating with thiourea gives polyfluorinated oxathiacalixarenes containing six and five aromatic nuclei, respectively. |
format | Online Article Text |
id | pubmed-7864041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78640412021-02-06 Synthesis of Polyfluorinated Thia- and Oxathiacalixarenes Based on Perfluoro-m-xylene Kovtonyuk, Vladimir N. Gatilov, Yuri V. Nikul’shin, Pavel V. Bredikhin, Roman A. Molecules Article Perfluorinated tetrathiacalix[4]arene was obtained by heating perfluoro-m-xylene with thiourea or 2,5-difluoro-4,6-bis(trifluoromethyl)benzene-1,3-dithiol at 90 °C. Interaction of perfluoro-m-xylene with resorcinol or orcinol under mild conditions and subsequent heating of the mixture with 2,5-difluoro-4,6-bis(trifluoromethyl)benzene-1,3-dithiol leads to polyfluorinated dioxadithiacalix[4]arenes. Triphenyl and pentaphenyl ethers formed by the interaction of perfluoro-m-xylene with resorcinol under heating with thiourea gives polyfluorinated oxathiacalixarenes containing six and five aromatic nuclei, respectively. MDPI 2021-01-20 /pmc/articles/PMC7864041/ /pubmed/33498335 http://dx.doi.org/10.3390/molecules26030526 Text en © 2021 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kovtonyuk, Vladimir N. Gatilov, Yuri V. Nikul’shin, Pavel V. Bredikhin, Roman A. Synthesis of Polyfluorinated Thia- and Oxathiacalixarenes Based on Perfluoro-m-xylene |
title | Synthesis of Polyfluorinated Thia- and Oxathiacalixarenes Based on Perfluoro-m-xylene |
title_full | Synthesis of Polyfluorinated Thia- and Oxathiacalixarenes Based on Perfluoro-m-xylene |
title_fullStr | Synthesis of Polyfluorinated Thia- and Oxathiacalixarenes Based on Perfluoro-m-xylene |
title_full_unstemmed | Synthesis of Polyfluorinated Thia- and Oxathiacalixarenes Based on Perfluoro-m-xylene |
title_short | Synthesis of Polyfluorinated Thia- and Oxathiacalixarenes Based on Perfluoro-m-xylene |
title_sort | synthesis of polyfluorinated thia- and oxathiacalixarenes based on perfluoro-m-xylene |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864041/ https://www.ncbi.nlm.nih.gov/pubmed/33498335 http://dx.doi.org/10.3390/molecules26030526 |
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