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dc.rights.licenseopenen_US
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 2 LCPO : Biopolymers & Bio-sourced Polymers
dc.contributor.authorDEL RÍO, Enrique
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 2 LCPO : Biopolymers & Bio-sourced Polymers
dc.contributor.authorVIDIL, Thomas
IDREF: 187905878
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 2 LCPO : Biopolymers & Bio-sourced Polymers
dc.contributor.authorGATI, Wafa
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 2 LCPO : Biopolymers & Bio-sourced Polymers
dc.contributor.authorGRAU, Etienne
IDREF: 187909261
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 1 LCPO : Polymerization Catalyses & Engineering
dc.contributor.authorTATON, Daniel
hal.structure.identifierLaboratoire de Caractérisation Physique Off-line [LCPO]
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 2 LCPO : Biopolymers & Bio-sourced Polymers
hal.structure.identifierFédération de recherche INCREASE [INCREASE]
dc.contributor.authorCRAMAIL, Henri
dc.date.accessioned2021-11-22T18:39:23Z
dc.date.available2021-11-22T18:39:23Z
dc.date.issued2021-09-08
dc.identifier.issn2168-0485en_US
dc.identifier.urioai:crossref.org:10.1021/acssuschemeng.1c05122
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/123917
dc.description.abstractEnThe need to take into account the life cycle of ionic liquids (ILs), from the sourcing of the raw materials involved in their synthesis to their disposal and degradation, has become paramount in the design of new IL-type molecular structures. In the case of 1-alkyl-3-methylimidazolium salts, one of the prominent IL families, there is an increasing demand for synthetic methods involving (i) substitution of the petro-based alkyl derivatives by readily available bio-sourced surrogates and (ii) functionalization of the alkyl tail with heterofunctional groups enabling the (bio)degradation of ILs after use. Herein, a straightforward and industrially viable synthesis of lipidic imidazolium salts is reported, starting from different bio-sourced fatty alcohols, including oleic, stearyl, and lauryl alcohols. This procedure is based on the acrylation of fatty alcohols, followed by the aza-Michael addition of the imidazole group onto the acrylate moiety. Subsequent quaternization, using either methyl iodide or methyl tosylate, provides a library of 1-alkylpropionate-3-methylimidazolium salts with various alkyl chain lengths (C18, C12, and C11) and incorporating different types of counteranions (iodide, tosylate, and tetrafluoroborate). These ester-containing analogues of classical 1-alkyl-3-methylimidazolium salts are all ILs, that is, with a melting point below 100 °C. In addition, most of them exhibit a liquid-crystal behavior and can be referred to as IL crystals (ILCs). The thermal stability, as well as the phase transitions of these ILs, has been investigated by thermogravimetric analysis, as well as differential scanning calorimetry, respectively, while the molecular structure into the crystalline phase and the mesophase is studied by X-ray scattering. Interestingly, ILCs featuring unsaturated alkyl tails exhibit a low melting point, close to room temperature, and the presence of the ester function is shown to provide an enhanced stabilization of the mesophase.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial-ShareAlike 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/us/*
dc.sourcecrossref
dc.title.enEster-Containing Imidazolium-Type Ionic Liquid Crystals Derived from Bio-based Fatty Alcohols
dc.typeArticle de revueen_US
dc.identifier.doi10.1021/acssuschemeng.1c05122en_US
dc.subject.halChimie/Polymèresen_US
bordeaux.journalACS Sustainable Chemistry & Engineeringen_US
bordeaux.page12687-12698en_US
bordeaux.volume9en_US
bordeaux.issue37en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcedissemin
hal.identifierhal-03455692
hal.version1
hal.date.transferred2021-11-29T17:13:45Z
hal.exporttrue
workflow.import.sourcedissemin
dc.rights.ccCC BY-NC-SAen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=ACS%20Sustainable%20Chemistry%20&%20Engineering&rft.date=2021-09-08&rft.volume=9&rft.issue=37&rft.spage=12687-12698&rft.epage=12687-12698&rft.eissn=2168-0485&rft.issn=2168-0485&rft.au=DEL%20R%C3%8DO,%20Enrique&VIDIL,%20Thomas&GATI,%20Wafa&GRAU,%20Etienne&TATON,%20Daniel&rft.genre=article


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