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Perfluoropyridine: Discovery, Chemistry, and Applications in Polymers and Material Science
Perfluoropyridine (PFPy) is an organofluorine compound that has been employed for a variety of applications, from straightforward chemical synthesis to more advanced functions, such as fluorinated networks and polymers. This can be directly attributed to the highly reactive nature of PFPy, especiall...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911800/ https://www.ncbi.nlm.nih.gov/pubmed/35268717 http://dx.doi.org/10.3390/molecules27051616 |
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author | Gautam, Ritesh Geniza, Ian Iacono, Scott T. Friesen, Chadron M. Jennings, Abby R. |
author_facet | Gautam, Ritesh Geniza, Ian Iacono, Scott T. Friesen, Chadron M. Jennings, Abby R. |
author_sort | Gautam, Ritesh |
collection | PubMed |
description | Perfluoropyridine (PFPy) is an organofluorine compound that has been employed for a variety of applications, from straightforward chemical synthesis to more advanced functions, such as fluorinated networks and polymers. This can be directly attributed to the highly reactive nature of PFPy, especially towards nucleophilic aromatic substitution (SNAr). The aim of this review is to highlight the discovery and synthesis of PFPy, discuss its reactive nature towards SNAr, and to summarize known reports of the utilization and thermal analysis of PFPy containing fluoropolymers and fluorinated network materials. |
format | Online Article Text |
id | pubmed-8911800 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89118002022-03-11 Perfluoropyridine: Discovery, Chemistry, and Applications in Polymers and Material Science Gautam, Ritesh Geniza, Ian Iacono, Scott T. Friesen, Chadron M. Jennings, Abby R. Molecules Review Perfluoropyridine (PFPy) is an organofluorine compound that has been employed for a variety of applications, from straightforward chemical synthesis to more advanced functions, such as fluorinated networks and polymers. This can be directly attributed to the highly reactive nature of PFPy, especially towards nucleophilic aromatic substitution (SNAr). The aim of this review is to highlight the discovery and synthesis of PFPy, discuss its reactive nature towards SNAr, and to summarize known reports of the utilization and thermal analysis of PFPy containing fluoropolymers and fluorinated network materials. MDPI 2022-02-28 /pmc/articles/PMC8911800/ /pubmed/35268717 http://dx.doi.org/10.3390/molecules27051616 Text en © 2022 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 Gautam, Ritesh Geniza, Ian Iacono, Scott T. Friesen, Chadron M. Jennings, Abby R. Perfluoropyridine: Discovery, Chemistry, and Applications in Polymers and Material Science |
title | Perfluoropyridine: Discovery, Chemistry, and Applications in Polymers and Material Science |
title_full | Perfluoropyridine: Discovery, Chemistry, and Applications in Polymers and Material Science |
title_fullStr | Perfluoropyridine: Discovery, Chemistry, and Applications in Polymers and Material Science |
title_full_unstemmed | Perfluoropyridine: Discovery, Chemistry, and Applications in Polymers and Material Science |
title_short | Perfluoropyridine: Discovery, Chemistry, and Applications in Polymers and Material Science |
title_sort | perfluoropyridine: discovery, chemistry, and applications in polymers and material science |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911800/ https://www.ncbi.nlm.nih.gov/pubmed/35268717 http://dx.doi.org/10.3390/molecules27051616 |
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