New design of polyphenylene dendrimers for full-color light-emitting diodes

dc.contributor.authorQin, Tianshi
dc.date.accessioned2010-04-08T13:49:28Z
dc.date.available2010-04-08T15:49:28Z
dc.date.issued2010
dc.description.abstractDendritic systems, and in particular polyphenylene dendrimers, have recently attracted considerable attention from the synthetic organic chemistry community, as well as from photophysicists, particularly in view of the search for synthetic model analogies to photoelectric materials to fabricate organic light-emitting diodes (OLEDs), and even more advanced areas of research such as light-harvesting system, energy transfer and non-host device. Geometrically, dendrimers are unique systems that consist of a core, one or more dendrons, and surface groups. The different parts of the macromolecule can be selected to give the desired optoelectronic and processing properties. Compared to small molecular or polymeric light-emitting materials, these dendritic materials can combine the benefits of both previous classes. The high molecular weights of these dendritic macromolecules, as well as the surface groups often attached to the distal ends of the dendrons, can improve the solution processability, and thus can be deposited from solution by simple processes such as spin-coating and ink-jet printing. Moreover, even better than the traditional polymeric light-emitting materials, the well-defined monodisperse distributed dendrimers possess a high purity comparable to that of small molecules, and as such can be fabricated into high performance OLEDs. Most importantly, the emissive chromophores can be located at the core of the dendrimer, within the dendrons, and/or at the surface of the dendrimers because of their unique dendritic architectures. The different parts of the macromolecule can be selected to give the desired optoelectronic and processing properties. Therefore, the main goals of this thesis are the design and synthesis, characterization of novel functional dendrimers, e.g. polytriphenylene dendrimers for blue fluorescent, as well as iridium(III) complex cored polyphenylene dendrimers for green and red phosphorescent light emitting diodes. In additional to the above mentioned advantages of dendrimer based OLEDs, the modular molecular architecture and various functionalized units at different locations in polyphenylene dendrimers open up a tremendous scope for tuning a wide range of properties in addition to color, such as intermolecular interactions, charge mobility, quantum yield, and exciton diffusion. In conclusion, research into dendrimer containing OLEDs combines fundamental aspects of organic semiconductor physics, novel and highly sophisticated organic synthetic chemistry and elaborate device technology.rnen_GB
dc.identifier.doihttp://doi.org/10.25358/openscience-2246
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/2248
dc.identifier.urnurn:nbn:de:hebis:77-22338
dc.language.isoeng
dc.rightsInC-1.0de_DE
dc.rights.urihttps://rightsstatements.org/vocab/InC/1.0/
dc.subject.ddc540 Chemiede_DE
dc.subject.ddc540 Chemistry and allied sciencesen_GB
dc.titleNew design of polyphenylene dendrimers for full-color light-emitting diodesen_GB
dc.typeDissertationde_DE
jgu.description.extent205 S.
jgu.organisation.departmentFB 09 Chemie, Pharmazie u. Geowissensch.
jgu.organisation.nameJohannes Gutenberg-Universität Mainz
jgu.organisation.number7950
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.organisation.year2010
jgu.rights.accessrightsopenAccess
jgu.subject.ddccode540
jgu.type.dinitypePhDThesis
jgu.type.resourceText
jgu.type.versionOriginal worken_GB
opus.date.accessioned2010-04-08T13:49:28Z
opus.date.available2010-04-08T15:49:28
opus.date.modified2010-04-13T12:10:55Z
opus.identifier.opusid2233
opus.institute.number0905
opus.metadataonlyfalse
opus.organisation.stringFB 09: Chemie, Pharmazie und Geowissenschaften: Institut für Organische Chemiede_DE
opus.subject.dfgcode00-000
opus.subject.otherdendrimer , OLED , phosphorescent , fluorescent , RGBen_GB
opus.type.contenttypeDissertationde_DE
opus.type.contenttypeDissertationen_GB

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