Bulk Organocatalytic Synthetic Access to Statistical Copolyesters from l-Lactide and ε-Caprolactone Using Benzoic Acid
dc.rights.license | open | |
hal.structure.identifier | Laboratoire de Chimie des Polymères Organiques [LCPO] | |
hal.structure.identifier | Team 1 LCPO : Polymerization Catalyses & Engineering | |
dc.contributor.author | MEZZASALMA, Leila | |
hal.structure.identifier | Interactions moléculaires et réactivité chimique et photochimique [IMRCP] | |
dc.contributor.author | HARRISSON, Simon | |
hal.structure.identifier | Nutrition, Métabolismes et Cancer [NuMeCan] | |
dc.contributor.author | SABA, Saad | |
hal.structure.identifier | Nutrition, Métabolismes et Cancer [NuMeCan] | |
dc.contributor.author | LOYER, Pascal | |
dc.contributor.author | COULEMBIER, Olivier | |
hal.structure.identifier | Laboratoire de Chimie des Polymères Organiques [LCPO] | |
hal.structure.identifier | Team 1 LCPO : Polymerization Catalyses & Engineering | |
dc.contributor.author | TATON, Daniel | |
dc.date.accessioned | 2020 | |
dc.date.available | 2020 | |
dc.date.issued | 2019 | |
dc.identifier.issn | 1525-7797 | |
dc.identifier.uri | https://oskar-bordeaux.fr/handle/20.500.12278/19847 | |
dc.description.abstractEn | The development of synthetic strategies to produce statistical copolymers based on l-lactide (l-LA) and ε-caprolactone (CL), denoted as P(LA- stat-CL), remains highly challenging in polymer chemistry. This is due to the differing reactivity of the two monomers during their ring-opening copolymerization (ROcP). Yet, P(LA- stat-CL) materials are highly sought after as they combine the properties of both polylactide (PLA) and poly(ε-caprolactone) (PCL). Here, benzoic acid (BA), a naturally occurring, cheap, readily recyclable, and thermally stable weak acid, is shown to trigger the organocatalyzed ring-opening copolymerization (OROcP) of l-LA and CL under solvent-free conditions at 155 °C, in presence of various alcohols as initiators, with good control over molar masses and dispersities (1.11 < Đ < 1.35) of the resulting copolyesters. Various compositions can be achieved, and the formation of statistical compounds is shown through characterization by H, C, and diffusion ordered spectroscopy NMR spectroscopies and by differential scanning calorimetry, as well as through the determination of reactivity ratios ( r = 0.86, r = 0.86), using the visualization of the sum of squared residuals space method. Furthermore, this BA-OROcP process can be exploited to access metal-free PLA- b-P(LA- stat-CL)- b-PLA triblock copolymers, using a diol as an initiator. Finally, residual traces of BA remaining in P(LA- stat-CL) copolymers (<0.125 mol %) do not show any cytotoxicity toward hepatocyte-like HepaRG cells, demonstrating the safety of this organic catalyst. | |
dc.language.iso | en | |
dc.publisher | American Chemical Society | |
dc.subject.en | bulk | |
dc.subject.en | organocatalysis | |
dc.subject.en | benzoic acid | |
dc.subject.en | lactide | |
dc.subject.en | caprolactone | |
dc.subject.en | copolymerization | |
dc.subject.en | statistical copolymers | |
dc.title.en | Bulk Organocatalytic Synthetic Access to Statistical Copolyesters from l-Lactide and ε-Caprolactone Using Benzoic Acid | |
dc.type | Article de revue | |
dc.identifier.doi | 10.1021/acs.biomac.9b00190 | |
dc.subject.hal | Chimie/Polymères | |
dc.description.sponsorshipEurope | European Joint Doctorate in Organocatalysis and Sustainable Polymers | |
bordeaux.journal | Biomacromolecules | |
bordeaux.page | 1965-1974 | |
bordeaux.volume | 20 | |
bordeaux.hal.laboratories | Laboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629 | * |
bordeaux.issue | 5 | |
bordeaux.institution | Bordeaux INP | |
bordeaux.institution | Université de Bordeaux | |
bordeaux.peerReviewed | oui | |
hal.identifier | hal-02120885 | |
hal.version | 1 | |
hal.origin.link | https://hal.archives-ouvertes.fr//hal-02120885v1 | |
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