Cationic clustering influences the phase behaviour of ionic liquids

dc.bibliographicCitation.firstPage14753
dc.bibliographicCitation.issue1
dc.bibliographicCitation.journalTitleScientific Reportseng
dc.bibliographicCitation.volume8
dc.contributor.authorNiemann, Thomas
dc.contributor.authorZaitsau, Dimitri
dc.contributor.authorStrate, Anne
dc.contributor.authorVillinger, Alexander
dc.contributor.authorLudwig, Ralf
dc.date.accessioned2023-04-27T11:59:30Z
dc.date.available2023-04-27T11:59:30Z
dc.date.issued2018
dc.description.abstract“Unlike charges attract, but like charges repel”. This conventional wisdom has been recently challenged for ionic liquids. It could be shown that like-charged ions attract each other despite the powerful opposing electrostatic forces. In principle, cooperative hydrogen bonding between ions of like-charge can overcome the repulsive Coulomb interaction while pushing the limits of chemical bonding. The key challenge of this solvation phenomenon is to establish design principles for the efficient formation of clusters of like-charged ions in ionic liquids. This is realised here for a set of well-suited ionic liquids including the same hydrophobic anion but different cations all equipped with hydroxyethyl groups for possible H-bonding. The formation of H-bonded cationic clusters can be controlled by the delocalization of the positive charge on the cations. Strongly localized charge results in cation-anion interaction, delocalized charge leads to the formation of cationic clusters. For the first time we can show, that the cationic clusters influence the properties of ILs. ILs comprising these clusters can be supercooled and form glasses. Crystalline structures are obtained only, if the ILs are dominantly characterized by the attraction between opposite-charged ions resulting in conventional ion pairs. That may open a new path for controlling glass formation and crystallization. The glass temperatures and the phase transitions of the ILs are observed by differential scanning calorimetry (DSC) and infrared (IR) spectroscopy.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/12131
dc.identifier.urihttp://dx.doi.org/10.34657/11165
dc.language.isoeng
dc.publisherLondon : Nature Publishing Group
dc.relation.doihttps://doi.org/10.1038/s41598-018-33176-6
dc.relation.essn2045-2322
dc.rights.licenseCC BY 4.0 Unported
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subject.ddc500
dc.subject.ddc600
dc.subject.otherCluster Cationseng
dc.subject.otherIonic Liquidseng
dc.subject.otherLike-charged Ionseng
dc.subject.otherEstablished Design Principleseng
dc.subject.otherCyclic Tetramereng
dc.titleCationic clustering influences the phase behaviour of ionic liquidseng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccess
wgl.contributorLIKAT
wgl.subjectChemieger
wgl.typeZeitschriftenartikelger
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