Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-1962
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dc.contributor.authorLorbach, Dominik Wilhelm
dc.date.accessioned2016-02-12T16:29:19Z
dc.date.available2016-02-12T17:29:19Z
dc.date.issued2016
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/1964-
dc.description.abstractIn this dissertation a novel class of pyrene copolymers is presented. Thereby this novel class of polymers shows deep blue light emission as required for OLEDs and does not exhibit excimer or aggregate emission when processed in films. Moreover the optical properties of the compounds are found to be comparable to that of well-known blue emitting conjugated polymers and significantly enhanced compared to their neat homopolymers. OLEDs built in an improved device assembly show stable bright blue emission. A considerable efficiency enhancement can be demonstrated using new charge carrier layer in the device assembly. In the second part of this contribution 1,3 , 1,4 and 4,10 connected pyrenylene compounds are synthesized and cyclodehydrogenated to their corresponding polyaromatic hydrocarbons. Thereby the first synthesis of the macrocycle cyclohexa(1,3‐pyrenylene) is achieved in six steps starting with pyrene and leading to a non‐aggregating highly twisted blue‐light‐emitting material. As well this work subject bi- and terpyrenyls to selective fusion for formation of extended polycyclic aromatic hydrocarbons (PAHs). Connecting the pyrene units at 4-4′- or 1-4′-positions led to smooth formation of extended PAHs, achieved via cyclodehydrogenation. This is far more difficult if pyrene is coupled in the 1,1′-position.en_GB
dc.language.isoger
dc.rightsInCopyrightde_DE
dc.rights.urihttps://rightsstatements.org/vocab/InC/1.0/
dc.subject.ddc540 Chemiede_DE
dc.subject.ddc540 Chemistry and allied sciencesen_GB
dc.title1,3- und 4,10-Verknüpfte Pyrenylene: Grundkörper für konjugierte Polymere und polyaromatische Kohlenwasserstoffede_DE
dc.typeDissertationde_DE
dc.identifier.urnurn:nbn:de:hebis:77-diss-1000002466
dc.identifier.doihttp://doi.org/10.25358/openscience-1962-
jgu.type.dinitypedoctoralThesis
jgu.type.versionOriginal worken_GB
jgu.type.resourceText
jgu.description.extent239 S.
jgu.organisation.departmentFB 09 Chemie, Pharmazie u. Geowissensch.-
jgu.organisation.year2015
jgu.organisation.number7950-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.organisation.placeMainz-
jgu.subject.ddccode540
opus.date.accessioned2016-02-12T16:29:19Z
opus.date.modified2016-03-11T12:01:52Z
opus.date.available2016-02-12T17:29:19
opus.subject.dfgcode00-000
opus.organisation.stringFB 09: Chemie, Pharmazie und Geowissenschaften: Institut für Organische Chemiede_DE
opus.identifier.opusid100000246
opus.institute.number0905
opus.metadataonlyfalse
opus.type.contenttypeDissertationde_DE
opus.type.contenttypeDissertationen_GB
jgu.organisation.rorhttps://ror.org/023b0x485
Appears in collections:JGU-Publikationen

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