0000000000003990

AUTHOR

Christophe M. Thomas

0000-0001-8014-4255

showing 3 related works from this author

Facile and efficient chemical functionalization of aliphatic polyesters by cross metathesis

2016

International audience; An effective preparation of new tailor-made macromolecular materials via a combination of two (atom-efficient) catalytic transformations is reported. First, new aliphatic polyesters with alternated composition have been prepared using a salen aluminum catalyst system. Next, the pendant vinyl moieties in those copolymers have been selectively transformed into various functional groups by metathesis in the presence of homogeneous Grubbs catalysts. The latter metathesis reaction has been optimized in terms of catalytic activity and selectivity, to define the conditions for an effective and safe procedure that does not affect the macromolecular architecture. All polymer …

plga microspheresphosphate-buffered solutionin-vivo degradationPolymers and PlasticsBioengineeringmolecular-weight poly(l-lactide)010402 general chemistryMetathesis01 natural sciencesBiochemistry[ CHIM ] Chemical SciencesCatalysisacid) microspheresCopolymerSalt metathesis reactionenzymatic degradation[CHIM]Chemical SciencesOrganic chemistryRing-opening metathesis polymerisationcyclic anhydrides010405 organic chemistryChemistryring-opening copolymerizationOrganic Chemistryrenewable resources0104 chemical sciencesPolyester[ CHIM.POLY ] Chemical Sciences/Polymers[CHIM.POLY]Chemical Sciences/Polymersbiodegradable polymersSelectivityAcyclic diene metathesis
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Multicatalytic Transformation of (Meth)acrylic Acids: a One-Pot Approach to Biobased Poly(meth)acrylates

2021

International audience; Shifting from petrochemical feedstocks to renewable resources can address some of the environmental issues associated with petrochemical extraction and make plastics production sustainable. Therefore, there is a growing interest in selective methods for transforming abundant renewable feedstocks into monomers suitable for polymer production. Reported herein are one-pot catalytic systems, that are active,<br&gtproductive, and selective under mild conditions for the synthesis of copolymers from renewable materials. Each system allows for anhydride formation, alcohol acylation and/or acid esterification, as well as polymerization of the formed (meth)- acrylates, providi…

[CHIM.POLY] Chemical Sciences/Polymers010402 general chemistry7. Clean energy01 natural sciencesCatalysisAcylationchemistry.chemical_compoundCopolymerOrganic chemistrychemistry.chemical_classification[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistry[CHIM.CATA] Chemical Sciences/CatalysisGeneral ChemistryPolymerMeth-[CHIM.CATA]Chemical Sciences/CatalysisGeneral Medicine[PHYS.MECA]Physics [physics]/Mechanics [physics][CHIM.ORGA] Chemical Sciences/Organic chemistry0104 chemical sciencesMonomerPetrochemical[CHIM.POLY]Chemical Sciences/PolymerschemistryPolymerization[PHYS.MECA] Physics [physics]/Mechanics [physics]Renewable resource
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Design and synthesis of biobased epoxy thermosets from biorenewable resources

2017

International audience; Biobased diepoxy synthons derived from isoeugenol, eugenol or resorcinol (DGE-isoEu, DGE-Eu and DGER, respectively) have been used as epoxy monomers in replacement of the diglycidyl ether of bisphenol A (DGEBA). Their curing with six different biobased anhydride hardeners leads to fully biobased epoxy thermosets. These materials exhibit interesting thermal and mechanical properties comparable to those obtained with conventional petrosourced DGEBA-based epoxy resins cured in similar conditions. In particular, a high Tg in the range of 90–130 °C and instantaneous moduli higher than 4.3 GPa have been recorded. These good performances are very encouraging, making these n…

Bisphenol AMaterials scienceDiglycidyl etherGeneral Chemical EngineeringThermosetting polymer02 engineering and technologyResorcinol010402 general chemistry01 natural sciences[ CHIM ] Chemical SciencesNanoindentationchemistry.chemical_compound[CHIM] Chemical SciencesPolymer chemistry[CHIM]Chemical SciencesComputingMilieux_MISCELLANEOUSCuring (chemistry)Biobased resinsPolymer scienceCuring process[CHIM.MATE]Chemical Sciences/Material chemistryGeneral ChemistryEpoxy021001 nanoscience & nanotechnology0104 chemical sciencesDEGBA alternativeIsoeugenolMonomerchemistryvisual_artvisual_art.visual_art_medium0210 nano-technologyEpoxy-anhydride thermosets
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