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dc.contributor.advisorZysman-Colman, Eli
dc.contributor.advisorGuerchais, Véronique
dc.contributor.authorHierlinger, Claus
dc.coverage.spatialxxix, 246 p.en_US
dc.date.accessioned2018-10-02T13:51:56Z
dc.date.available2018-10-02T13:51:56Z
dc.date.issued2018-12-06
dc.identifier.urihttp://hdl.handle.net/10023/16126
dc.description.abstractHere, the design, synthesis and characterisation and the optoelectronic properties of Ir(III) complexes for application in nonlinear optical and electroluminescent devices are described. The type of complexes varies from those of the form [Ir(C^N)₂(N^N)]+ with conjugated and nonconjugated ligands (where C^N = cyclometalating ligand and N^N = neutral ligand) to those of the form [Ir(C^N^C)(N^N)Cl] (where C^N^C = tridentate tripod ligand). Chapter 1 gives an introduction into photophysics occurring in transition metal complexes and possible applications in visual displays. The background of nonlinear optical (NLO) properties and the use of transition metal complexes as NLO chromophores is described. In Chapter 2, the impact of the use of sterically congested cyclometalating ligands on the photoluminescence properties of cationic iridium(III) complexes and their performance in light-emitting electrochemical cells is investigated. Chapter 3 explores the use of electron donors on the cyclometalating ligand towards modulating the NLO properties of the complexes. Combining strongly electron-donating substituents on the C^N ligand and electron-accepting substituents on the N^N ligand results in strong NLO activity. Chapter 4 summarises a new series of cationic iridium(III) complexes bearing benzylpyridinato as cyclometalating ligands. The methylene spacer in the C^N ligands provides flexibility, resulting in two conformers. NMR studies combined with density functional theory (DFT) studies show how the fluxional behaviour is influenced by the choice of the ancillary ligand. In Chapter 5, Ir(III) complexes bearing an unusual nonconjugated bis(six-membered) tridentate tripod ligand of the form [Ir(C^N^C)(N^N)Cl] are introduced. Depending on the substitutions of the C^N^C ligand phosphorescence ranging from yellow to red was obtained. Substitution of the N^N results in a panchromatic NIR dye, suitable for DSSC applications. In Chapter 6, the concept of a nonconjugated ligand was expanded to the N^N ligand. Blue-green and sky-blue emission was obtained, demonstrating a strategy to successfully tune the emission to the blue.en_US
dc.description.sponsorship"This work was supported by Région Bretagne and EPSRC (EP/M02105X/1)" -- Acknowledgementsen
dc.language.isoenen_US
dc.publisherUniversity of St Andrews
dc.relationSynthesis, characterisation and optoelectronic properties of phosphorescent iridium complexes: from five to six-membered ring chelates (Thesis data) Hierlinger, C., University of St Andrews, 2019. DOI: https://doi.org/10.17630/b641a08a-a98c-4bbc-a1f6-5cadcbb69cc8en
dc.relation.urihttps://doi.org/10.17630/b641a08a-a98c-4bbc-a1f6-5cadcbb69cc8
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectIridiumen_US
dc.subjectPhotoluminescenceen_US
dc.subject.lccQD412.I7H5
dc.subject.lcshIridium compounds--Synthesisen
dc.subject.lcshIridium compounds--Analysisen
dc.subject.lcshIridium compounds--Optical propertiesen
dc.subject.lcshPhosphorescenceen
dc.subject.lcshComplex compoundsen
dc.titleSynthesis, characterisation and optoelectronic properties of phosphorescent iridium complexes : from five to six-membered ring chelatesen_US
dc.typeThesisen_US
dc.contributor.sponsorEngineering and Physical Sciences Research Council (EPSRC)en_US
dc.contributor.sponsorBrittany (France)en_US
dc.type.qualificationlevelDoctoralen_US
dc.type.qualificationnamePhD Doctor of Philosophyen_US
dc.publisher.institutionThe University of St Andrewsen_US
dc.publisher.departmentUniversité de Rennes 1en_US


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