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Strategies for the synthesis of fluorinated polyesters

In this work we synthetized three fluorinated polyesters from dimethyl tetrafluorosuccinate (DMTFS), dimethyl hexafluoroglutarate (DMHFG), and dimethyl octafluoroadipate (DMOFA) and ethylene glycol. The influence of parameters like monomer's size, temperature, vacuum, ultrasound and catalyst, o...

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Autores principales: Zhao, Xiaoman, Noro, Jennifer, Fu, Jiajia, Silva, Carla, Cavaco-Paulo, Artur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059763/
https://www.ncbi.nlm.nih.gov/pubmed/35516098
http://dx.doi.org/10.1039/c8ra10341k
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author Zhao, Xiaoman
Noro, Jennifer
Fu, Jiajia
Silva, Carla
Cavaco-Paulo, Artur
author_facet Zhao, Xiaoman
Noro, Jennifer
Fu, Jiajia
Silva, Carla
Cavaco-Paulo, Artur
author_sort Zhao, Xiaoman
collection PubMed
description In this work we synthetized three fluorinated polyesters from dimethyl tetrafluorosuccinate (DMTFS), dimethyl hexafluoroglutarate (DMHFG), and dimethyl octafluoroadipate (DMOFA) and ethylene glycol. The influence of parameters like monomer's size, temperature, vacuum, ultrasound and catalyst, on the polyesters synthesis was evaluated. The conversion rates were assessed considering (1)H NMR data and the results disclose the role of ultrasound (US) as crucial to attain high reaction conversion rates (≈20% of increase relatively to the reactions performed in absence of US). The effect of US was more relevant for the higher molecular weight monomers (DMHFG and DMOFA). The use of Candida antarctica lipase (immobilized CALB) marginally favors the synthesis reactions when fixing the other conditions. The size of the starting monomers influenced greatly the reaction conversion rates, as shorter monomers gave rise to high amount of product recovering. All the produced polyesters were isolated and fully characterized by NMR ((1)H and (19)F), FTIR, TGA and MALDI-TOF.
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spelling pubmed-90597632022-05-04 Strategies for the synthesis of fluorinated polyesters Zhao, Xiaoman Noro, Jennifer Fu, Jiajia Silva, Carla Cavaco-Paulo, Artur RSC Adv Chemistry In this work we synthetized three fluorinated polyesters from dimethyl tetrafluorosuccinate (DMTFS), dimethyl hexafluoroglutarate (DMHFG), and dimethyl octafluoroadipate (DMOFA) and ethylene glycol. The influence of parameters like monomer's size, temperature, vacuum, ultrasound and catalyst, on the polyesters synthesis was evaluated. The conversion rates were assessed considering (1)H NMR data and the results disclose the role of ultrasound (US) as crucial to attain high reaction conversion rates (≈20% of increase relatively to the reactions performed in absence of US). The effect of US was more relevant for the higher molecular weight monomers (DMHFG and DMOFA). The use of Candida antarctica lipase (immobilized CALB) marginally favors the synthesis reactions when fixing the other conditions. The size of the starting monomers influenced greatly the reaction conversion rates, as shorter monomers gave rise to high amount of product recovering. All the produced polyesters were isolated and fully characterized by NMR ((1)H and (19)F), FTIR, TGA and MALDI-TOF. The Royal Society of Chemistry 2019-01-15 /pmc/articles/PMC9059763/ /pubmed/35516098 http://dx.doi.org/10.1039/c8ra10341k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Zhao, Xiaoman
Noro, Jennifer
Fu, Jiajia
Silva, Carla
Cavaco-Paulo, Artur
Strategies for the synthesis of fluorinated polyesters
title Strategies for the synthesis of fluorinated polyesters
title_full Strategies for the synthesis of fluorinated polyesters
title_fullStr Strategies for the synthesis of fluorinated polyesters
title_full_unstemmed Strategies for the synthesis of fluorinated polyesters
title_short Strategies for the synthesis of fluorinated polyesters
title_sort strategies for the synthesis of fluorinated polyesters
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059763/
https://www.ncbi.nlm.nih.gov/pubmed/35516098
http://dx.doi.org/10.1039/c8ra10341k
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AT silvacarla strategiesforthesynthesisoffluorinatedpolyesters
AT cavacopauloartur strategiesforthesynthesisoffluorinatedpolyesters