Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/30679
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dc.contributor.authorQUINTENS, Greg-
dc.contributor.authorVRIJSEN, Jeroen-
dc.contributor.authorADRIAENSENS, Peter-
dc.contributor.authorVANDERZANDE, Dirk-
dc.contributor.authorJUNKERS, Tanja-
dc.date.accessioned2020-03-05T14:40:57Z-
dc.date.available2020-03-05T14:40:57Z-
dc.date.issued2019-
dc.date.submitted2020-03-05T14:38:35Z-
dc.identifier.citationPolymer Chemistry, 10 (40) , p. 5555 -5563-
dc.identifier.urihttp://hdl.handle.net/1942/30679-
dc.description.abstractOver the course of the last century, a large number of synthetic polymers has been developed and introduced. Yet, most polymer materials are based on fossil fuels as raw materials and are associated with a considerable environmental impact. trans,trans-Muconic acid esters are interesting plant-based mono-mers that have not received much attention yet. The synthesis of a series of dialkyl muconates from muconic acid is described, followed by an optimization of the solution free-radical polymerization of these monomers. Unlike the claim in previous studies, dialkyl muconates can be polymerized efficiently in solution to polymers with significant molecular weights above 10 5 g mol −1. Polymerizations are, however, relatively slow, as can be expected for diene monomers (48 h at 120 °C). Mark-Houwink coefficients have been determined for diethyl muconate, dibutyl muconate and di(2-ethylhexyl) muconate. Furthermore, glass transition temperatures and thermal stability are assessed for the polymers, showcasing that poly-muconates can serve as alternatives to polyacrylate materials. In a last step, also the reversible addition-fragmentation chain transfer (RAFT) polymerization of the muconates is investigated, showing excellent control over the molecular weight when a conventional trithiocarbonate is used to control polymerizations.-
dc.description.sponsorshipThis work was performed in the framework of the Catalisti cluster SBO project SPICY (“Sugar-based chemicals and Polymers through Innovative Chemocatalysis and engineered Yeast”), with the financial support from VLAIO (Flemisch Agency for Innovation and Entrepeneurship).-
dc.language.isoen-
dc.publisher-
dc.rightsThe Royal Society of Chemistry 2019-
dc.titleMuconic acid esters as bio-based acrylate mimics-
dc.typeJournal Contribution-
dc.identifier.epage5563-
dc.identifier.issue40-
dc.identifier.spage5555-
dc.identifier.volume10-
local.bibliographicCitation.jcatA1-
local.publisher.placeTHOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND-
local.type.refereedRefereed-
local.type.specifiedArticle-
dc.source.typeArticle-
dc.identifier.doi10.1039/c9py01313j-
dc.identifier.isiWOS:000490292900011-
dc.identifier.eissn-
dc.identifier.eissn1759-9962-
local.provider.typePdf-
item.validationecoom 2020-
item.contributorQUINTENS, Greg-
item.contributorVRIJSEN, Jeroen-
item.contributorADRIAENSENS, Peter-
item.contributorVANDERZANDE, Dirk-
item.contributorJUNKERS, Tanja-
item.fullcitationQUINTENS, Greg; VRIJSEN, Jeroen; ADRIAENSENS, Peter; VANDERZANDE, Dirk & JUNKERS, Tanja (2019) Muconic acid esters as bio-based acrylate mimics. In: Polymer Chemistry, 10 (40) , p. 5555 -5563.-
item.fulltextWith Fulltext-
item.accessRightsRestricted Access-
crisitem.journal.issn1759-9954-
crisitem.journal.eissn1759-9962-
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