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dc.contributor.authorBalónová, Barbora
dc.contributor.authorRota Martir, Diego
dc.contributor.authorClark, Ewan
dc.contributor.authorShepherd, Helena
dc.contributor.authorZysman-Colman, Eli
dc.contributor.authorBlight, Barry
dc.date.accessioned2019-07-02T23:40:33Z
dc.date.available2019-07-02T23:40:33Z
dc.date.issued2018-07-03
dc.identifier.citationBalónová , B , Rota Martir , D , Clark , E , Shepherd , H , Zysman-Colman , E & Blight , B 2018 , ' Influencing the optoelectronic properties of a heteroleptic iridium complex by second-sphere H-bonding interactions ' , Inorganic Chemistry , vol. In press . https://doi.org/10.1021/acs.inorgchem.8b01326en
dc.identifier.issn0020-1669
dc.identifier.otherPURE: 253407447
dc.identifier.otherPURE UUID: 33238648-4bee-4ac9-a48a-79d60c3bdc85
dc.identifier.otherScopus: 85049954276
dc.identifier.otherORCID: /0000-0001-7183-6022/work/56639106
dc.identifier.otherWOS: 000439250500064
dc.identifier.urihttp://hdl.handle.net/10023/18027
dc.descriptionBAB is grateful for financial support from University of Kent, University of New Brunswick and New Brunswick Foundation for Innovation. EZ-C thanks the University of St Andrews and EPSRC (EP/M02105X/1) for financial support.en
dc.description.abstractThe use of a new second-sphere coordination methodology for emission color tuning of iridium complexes is presented. We demonstrate that a complimentary H-bonding guest molecule binding through contiguous triple H-bonding interactions can induce a shift in the emission of the iridium complex from green to blue without the need to alter the ligand structure around the metal centre, while simultaneously increasing the photoluminescence quantum yield in solution. The association constant for this host-guest interaction was determined to be Ka = 4.3 x 103 M-1 in a solution of 2% dimethylsulfoxide in chloroform by UV-Vis titration analysis and the impact of the hydrogen bonding interaction further probed by photoluminescence, electrochemical, and computational methods. Our findings suggest that directed self-assemblies are an effective approach to influencing emission properties of phosphorescent iridium (III) complexes.
dc.language.isoeng
dc.relation.ispartofInorganic Chemistryen
dc.rightsCopyright © 2018 American Chemical Society. This work has been made available online in accordance with the publisher’s policies. This is the author created accepted version manuscript following peer review and as such may differ slightly from the final published version. The final published version of this work is available at https://doi.org/10.1021/acs.inorgchem.8b01326en
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titleInfluencing the optoelectronic properties of a heteroleptic iridium complex by second-sphere H-bonding interactionsen
dc.typeJournal articleen
dc.description.versionPostprinten
dc.contributor.institutionUniversity of St Andrews.School of Chemistryen
dc.contributor.institutionUniversity of St Andrews.Organic Semiconductor Centreen
dc.contributor.institutionUniversity of St Andrews.EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1021/acs.inorgchem.8b01326
dc.description.statusPeer revieweden
dc.date.embargoedUntil2019-07-03


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