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dc.contributor.authorDolan, Andrew
dc.contributor.authorSherman, Dylan
dc.contributor.authorAtkin, Rob
dc.contributor.authorWarr, Gregory
dc.date.accessioned2019-06-17
dc.date.available2019-06-17
dc.date.issued2016-10-05
dc.identifier.citationChemPhysChem 2016, 17, 3096-3101. doi.org/10.1002/cphc.201600361en_AU
dc.identifier.issn1439-4235
dc.identifier.urihttp://hdl.handle.net/2123/20570
dc.description.abstractThe Kamlet-Taft solvent parameters of solvate ionic liquids (SILs) prepared from lithium salts with glyme and glycol ligands have been determined. The dipolarity/polarizibilities (π*) are high, similar to those found in conventional ionic liquids. The H-bond basicities (β) depend strongly on the anion. The H-bond acidities (α) are high in both glyme and glycol SILs, indicating that the lithium is acting as a H-bond donor site. ‘Poor’ SILs have glyme rich and salt rich regions, in these liquids the π* and β values are almost identical to the parent glyme or glycol, and the α values are determined by the salt alone.en_AU
dc.description.sponsorshipARCen_AU
dc.language.isoenen_AU
dc.publisherWiley - V C H Verlag GmbH & Co. KGaAen_AU
dc.relationARCen_AU
dc.rightsAuthors of articles published in ChemPhysChem are permitted to self-archive the accepted version after an embargo period of 12 months. The accepted version of an article is the version that incorporates all amendments made during the peer-review process, but prior to the final published version (Version of Record, which includes: copy and stylistic edits, online and print formatting, citation and other linking, deposit in abstracting and indexing services, and the addition of bibliographic and other material).en_AU
dc.subjectsolvate ionic liquiden_AU
dc.titleKamlet-Taft Solvation Parameters of Solvate Ionic Liquidsen_AU
dc.typeArticleen_AU
dc.subject.asrcFoR::030605 - Solution Chemistryen_AU
dc.identifier.doicphc.201600361
dc.type.pubtypePost-printen_AU


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