Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/58856

TitleStrategies for the synthesis of fluorinated polyesters
Author(s)Zhao, Xiaoman
Noro, Jennifer Martins
Fu, Jiajia
Silva, Carla
Cavaco-Paulo, Artur
Issue date2019
PublisherRoyal Society of Chemistry
JournalRSC Advances
CitationZhao, Xiaoman; Jennifer Noro; Fu, Jiajia; Silva, Carla; Cavaco-Paulo, Artur, Strategies for the synthesis of fluorinated polyesters. RSC Advances, 9, 1799-1806, 2019
Abstract(s)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 1H NMR data and the results disclose the role of ultrasound (US) as crucial to attain high reaction conversion rates (z20% 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 (1H and 19F), FTIR, TGA and MALDI-TOF.
TypeArticle
URIhttp://hdl.handle.net/1822/58856
DOI10.1039/c8ra10341k
ISSN2046-2069
e-ISSN2046-2069
Publisher versionhttp://pubs.rsc.org/en/journals/journalissues/ra
Peer-Reviewedyes
AccessOpen access
Appears in Collections:CEB - Publicações em Revistas/Séries Internacionais / Publications in International Journals/Series

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