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The role of charge transfer in the formation of type i deep eutectic solvent-analogous ionic liquid mixtures

dc.contributor.authorAbranches, Dinis O.
dc.contributor.authorSchaeffer, Nicolas
dc.contributor.authorSilva, Liliana P.
dc.contributor.authorMartins, Mónia A.R.
dc.contributor.authorPinho, Simão
dc.contributor.authorCoutinho, João A.P.
dc.date.accessioned2018-02-19T10:00:00Z
dc.date.accessioned2020-01-06T14:09:39Z
dc.date.available2018-01-19T10:00:00Z
dc.date.available2020-01-06T14:09:39Z
dc.date.issued2019
dc.description.abstractIt was recently shown that tetramethylammonium chloride presented negative deviations to ideality when mixed with tetraethylammonium chloride or tetrapropylammonium chloride, leading to a strong decrease of the melting points of these salt mixtures, in a behavior akin to that observed in the formation of deep eutectic solvents. To better rationalize this unexpected melting point depression between two structurally similar compounds devoid of dominant hydrogen bonding capability, new solid–liquid equilibria data for tetramethylammonium-based systems were measured and analyzed in this work. Molecular dynamics was used to show that the strong negative deviations from ideality presented by these systems arise from a synergetic share of the chloride ions. A transfer of chloride ions seems to occur from the bigger cation in the mixture (which possesses a more disperse charge) to the smaller cation (tetramethylammonium), resembling the formation of metal–chloride complexes in type I deep eutectic solvents. This rearrangement of the charged species leads to an energetic stabilization of both components in the mixture, inducing the negative deviations to the ideality observed. The conclusions presented herein emphasize the often-neglected contribution of charge delocalization in deep eutectic solvents formation and its applicability toward the design of new ionic liquid mixtures.
dc.description.sponsorshipThis work was developed in the scope of the project CICECO - Aveiro Institute of Materials, POCI-01-0145-FEDER-007679 (Ref. FCT UID/CTM/50011/2019) Associate Laboratory LSRE-LCM, POCI-01-0145-FEDER-006984 (Ref. FCT UID/EQU/50020/2019), and project MultiBiorefinery (POCI-01-0145-FEDER-016403), all financed by national funds through the FCT/MCTES (PIDDAC) and when appropriate co-financed by the FEDER under the PT2020 Partnership Agreement. M.A.R.M. acknowledges financial support from NORTE-01-0145-FEDER-000006 - funded by NORTE2020 through PT2020 and ERDF. L.P.S. acknowledges FCT for her PhD grant (SFRH/BD/135976/2018).
dc.description.versioninfo:eu-repo/semantics/publishedVersionen_EN
dc.identifier.citationAbranches, Dinis O.; Schaeffer, Nicolas; Silva, Liliana P.; Martins, Mónia A.R.; Pinho, Simão P.; Coutinho, João A.P. (2019). The role of charge transfer in the formation of type i deep eutectic solvent-analogous ionic liquid mixtures. Molecules. ISSN 1420-3049. 24, p. 1-15en_EN
dc.identifier.doi10.3390/molecules24203687en_EN
dc.identifier.urihttp://hdl.handle.net/10198/20241
dc.language.isoeng
dc.peerreviewedyesen_EN
dc.subjectCharge transferen_EN
dc.subjectDeep eutectic solventsen_EN
dc.subjectIonic liquid mixturesen_EN
dc.subjectMolecular dynamicsen_EN
dc.subjectQuaternary ammoniumen_EN
dc.subjectSolid-liquid equilibriaen_EN
dc.titleThe role of charge transfer in the formation of type i deep eutectic solvent-analogous ionic liquid mixturesen_EN
dc.typejournal article
dspace.entity.typePublication
person.familyNamePinho
person.givenNameSimão
person.identifier810882
person.identifier.ciencia-id481D-73AD-8D0F
person.identifier.orcid0000-0002-9211-857X
person.identifier.ridD-4148-2013
person.identifier.scopus-author-id7003570175
rcaap.rightsopenAccessen_EN
rcaap.typearticleen_EN
relation.isAuthorOfPublication8ef7789a-34f3-4915-a666-4efe26272a30
relation.isAuthorOfPublication.latestForDiscovery8ef7789a-34f3-4915-a666-4efe26272a30

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