Aliphatic polycarbonates and poly(ester carbonate)s from fatty acid derived monomers
dc.rights.license | open | |
hal.structure.identifier | Laboratoire de Chimie des Polymères Organiques [LCPO] | |
dc.contributor.author | MORE, Arvind S. | |
hal.structure.identifier | Laboratoire de Chimie des Polymères Organiques [LCPO] | |
dc.contributor.author | PALASKAR, Dnyaneshwar V | |
hal.structure.identifier | Laboratoire de Chimie des Polymères Organiques [LCPO] | |
hal.structure.identifier | Team 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies | |
dc.contributor.author | CLOUTET, Eric
IDREF: 151048681 | |
hal.structure.identifier | Institut des Corps Gras [ITERG] | |
dc.contributor.author | GADENNE, Benoît | |
hal.structure.identifier | Institut des Corps Gras [ITERG] | |
dc.contributor.author | ALFOS, Carine | |
hal.structure.identifier | Laboratoire de Chimie des Polymères Organiques [LCPO] | |
hal.structure.identifier | Team 2 LCPO : Biopolymers & Bio-sourced Polymers | |
dc.contributor.author | CRAMAIL, Henri | |
dc.date.accessioned | 2020 | |
dc.date.available | 2020 | |
dc.date.issued | 2011 | |
dc.identifier.issn | 1759-9954 | |
dc.identifier.uri | https://oskar-bordeaux.fr/handle/20.500.12278/20422 | |
dc.description.abstractEn | Fatty acid derivatives were efficiently used as starting materials for the synthesis of polycarbonates and poly(ester carbonate)s. A novel AB-type self-condensable monomer, ethyl(9-hydroxy-10-methoxyoctadecyl)carbonate (EHMOC) and a dicarbonate monomer, 4-[(ethoxycarbonyl)oxy]butyl-12-[(ethoxycarbonyl)oxy]octadec-9-enoate (EOBEOE) were prepared from oleyl alcohol and ricinoleic acid, respectively. Of these, EHMOC was polymerized by the alcohol-carbonate exchange self-polycondensation approach, while EOBEOE was polycondensed with various biobased diols to give polycarbonates and poly(ester carbonate) s, respectively. The monomers and polymers were well characterized by FTIR and H-1-NMR spectroscopy. The C-13-NMR spectroscopy revealed the formation of randomly distributed sequences in the poly(ester carbonate) s due to the carbonate interchange reaction. An unexpected formation of polyricinoleate was observed and confirmed by NMR and MALDI-TOF spectroscopy. Most of the polymers displayed good thermal stability with the temperature at 10% weight loss in the range 273-325 degrees C. Due to the presence of aliphatic segments, these materials exhibit very low glass transition temperature. | |
dc.language.iso | en | |
dc.publisher | Royal Society of Chemistry - RSC | |
dc.subject.en | POLYURETHANES | |
dc.subject.en | OIL | |
dc.subject.en | DIOLS | |
dc.subject.en | DIOXIDE | |
dc.subject.en | POLYMERS | |
dc.subject.en | RING-OPENING POLYMERIZATION | |
dc.subject.en | RENEWABLE RESOURCES | |
dc.subject.en | ALTERNATING COPOLYMERIZATION | |
dc.subject.en | CYCLIC CARBONATES | |
dc.subject.en | POLYESTERS | |
dc.title.en | Aliphatic polycarbonates and poly(ester carbonate)s from fatty acid derived monomers | |
dc.type | Article de revue | |
dc.identifier.doi | 10.1039/c1py00326g | |
dc.subject.hal | Chimie/Polymères | |
bordeaux.journal | Polymer Chemistry | |
bordeaux.page | 2796-2803 | |
bordeaux.volume | 2 | |
bordeaux.hal.laboratories | Laboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629 | * |
bordeaux.issue | 12 | |
bordeaux.institution | Bordeaux INP | |
bordeaux.institution | Université de Bordeaux | |
bordeaux.peerReviewed | oui | |
hal.identifier | hal-00818377 | |
hal.version | 1 | |
hal.origin.link | https://hal.archives-ouvertes.fr//hal-00818377v1 | |
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