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Are (Co)Polymers of 1,1,3,3,3-Pentafluoropropene Possible?

The copolymerization and terpolymerization of 1,1,3,3,3-pentafluoropropene (PFP) with various combinations of fluorinated and hydrogenated comonomers were investigated. The chosen fluoromonomers were vinylidene fluoride (VDF), 3,3,3-trifluoropropene (TFP), hexafluoropropene (HFP), perfluoromethylvin...

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Autores principales: Boschet, Frédéric, Kostov, Georgi, Raynova, Hristina, Améduri, Bruno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10304894/
https://www.ncbi.nlm.nih.gov/pubmed/37375173
http://dx.doi.org/10.3390/molecules28124618
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author Boschet, Frédéric
Kostov, Georgi
Raynova, Hristina
Améduri, Bruno
author_facet Boschet, Frédéric
Kostov, Georgi
Raynova, Hristina
Améduri, Bruno
author_sort Boschet, Frédéric
collection PubMed
description The copolymerization and terpolymerization of 1,1,3,3,3-pentafluoropropene (PFP) with various combinations of fluorinated and hydrogenated comonomers were investigated. The chosen fluoromonomers were vinylidene fluoride (VDF), 3,3,3-trifluoropropene (TFP), hexafluoropropene (HFP), perfluoromethylvinyl ether (PMVE), chlorotrifluoroethylene (CTFE) and tert-butyl-2-trifluoromethacrylate (MAF-TBE), while the hydrocarbon comonomers were vinylene carbonate (VCA), ethyl vinyl ether (EVE) and 3-isopropenyl-α,α-dimethylbenzyl isocyanate (m-TMI). Copolymers of PFP with non-homopolymerizable monomers (HFP, PMVE and MAF-TBE) led to quite low yields, while the introduction of VDF enabled the synthesis of poly(PFP-ter-VDF-ter-M(3)) terpolymers with improved yields. PFP does not homopolymerize and delays the copolymerizations. All polymers were either amorphous fluoroelastomers or fluorothermoplastics with glass transition temperatures ranging from −56 °C to +59 °C, and they exhibited good thermal stability in air.
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spelling pubmed-103048942023-06-29 Are (Co)Polymers of 1,1,3,3,3-Pentafluoropropene Possible? Boschet, Frédéric Kostov, Georgi Raynova, Hristina Améduri, Bruno Molecules Article The copolymerization and terpolymerization of 1,1,3,3,3-pentafluoropropene (PFP) with various combinations of fluorinated and hydrogenated comonomers were investigated. The chosen fluoromonomers were vinylidene fluoride (VDF), 3,3,3-trifluoropropene (TFP), hexafluoropropene (HFP), perfluoromethylvinyl ether (PMVE), chlorotrifluoroethylene (CTFE) and tert-butyl-2-trifluoromethacrylate (MAF-TBE), while the hydrocarbon comonomers were vinylene carbonate (VCA), ethyl vinyl ether (EVE) and 3-isopropenyl-α,α-dimethylbenzyl isocyanate (m-TMI). Copolymers of PFP with non-homopolymerizable monomers (HFP, PMVE and MAF-TBE) led to quite low yields, while the introduction of VDF enabled the synthesis of poly(PFP-ter-VDF-ter-M(3)) terpolymers with improved yields. PFP does not homopolymerize and delays the copolymerizations. All polymers were either amorphous fluoroelastomers or fluorothermoplastics with glass transition temperatures ranging from −56 °C to +59 °C, and they exhibited good thermal stability in air. MDPI 2023-06-07 /pmc/articles/PMC10304894/ /pubmed/37375173 http://dx.doi.org/10.3390/molecules28124618 Text en © 2023 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 Article
Boschet, Frédéric
Kostov, Georgi
Raynova, Hristina
Améduri, Bruno
Are (Co)Polymers of 1,1,3,3,3-Pentafluoropropene Possible?
title Are (Co)Polymers of 1,1,3,3,3-Pentafluoropropene Possible?
title_full Are (Co)Polymers of 1,1,3,3,3-Pentafluoropropene Possible?
title_fullStr Are (Co)Polymers of 1,1,3,3,3-Pentafluoropropene Possible?
title_full_unstemmed Are (Co)Polymers of 1,1,3,3,3-Pentafluoropropene Possible?
title_short Are (Co)Polymers of 1,1,3,3,3-Pentafluoropropene Possible?
title_sort are (co)polymers of 1,1,3,3,3-pentafluoropropene possible?
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10304894/
https://www.ncbi.nlm.nih.gov/pubmed/37375173
http://dx.doi.org/10.3390/molecules28124618
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