C 3-symmetric discotic liquid crystalline materials for molecular electronics: versatile synthesis and self-organization

dc.contributor.authorFeng, Xinliang
dc.date.accessioned2008-08-13T10:43:05Z
dc.date.available2008-08-13T12:43:05Z
dc.date.issued2008
dc.description.abstractThis thesis presents the versatile synthesis and self-organization of C3-symmetric discotic nanographene molecules as well as their potential applications as materials in molecular electronics. The details can be described as follows: 1) A novel synthetic strategy towards properly designed C3 symmetric 1,3,5-tris-2’arylbenzene precursors has been developed. After the final planarization by treatment with FeCl3 under mild conditions, for the first time, it became possible to access a variety of new C3-symmetric hexa-peri-hexabenzocoronenes (HBCs) and a series of triangle-shaped nanographenes. D3 symmetric HBC with three alkyl substituents and C2 symmetric HBC with two alkyl substituents were synthesized and found to show the surprising decrease of isotropic points., the self-assembly at the liquid-solid interface displayed a unique zigzag and flower patterns. 2) Triangle-shaped discotics revealed a unique self-assembly behavior in solution, solid state as well as at the solution-substrate interface. A mesophase stability over the broad temperature range with helical supramoelcular arrangement were observed in the bulk state. The honeycomb pattern as the result of novel self-assembly was presented. Triangle-shaped discotics with swallow alkyl tails were fabricated into photovoltaic devices, the supramolecular arrangement upon thermal treatment was found to play a key role in the improvement of solar efficiency. 3) A novel class of C3 symmetric HBCs with alternating polar/apolar substituents was synthesized. Their peculiar self-assembly in solution, in the bulk and on the surface were investigated by NMR techniques, X-ray diffraction as well as different electron microscope techniques. 4) A novel concept for manipulating the intracolumnar stacking of discotics and thus for controlling the helical pitch was presented. A unique staggered stacking in the column was achieved for the first time. Theoretical simulations confirmed this self- organization and predicted that this packing should show the highest charge carrier mobility for all discotics.en_GB
dc.identifier.doihttp://doi.org/10.25358/openscience-2623
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/2625
dc.identifier.urnurn:nbn:de:hebis:77-16996
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.titleC 3-symmetric discotic liquid crystalline materials for molecular electronics: versatile synthesis and self-organizationen_GB
dc.typeDissertationde_DE
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.year2008
jgu.rights.accessrightsopenAccess
jgu.subject.ddccode540
jgu.type.dinitypePhDThesis
jgu.type.resourceText
jgu.type.versionOriginal worken_GB
opus.date.accessioned2008-08-13T10:43:05Z
opus.date.available2008-08-13T12:43:05
opus.date.modified2008-08-13T10:43:05Z
opus.identifier.opusid1699
opus.institute.number0900
opus.metadataonlyfalse
opus.organisation.stringFB 09: Chemie, Pharmazie und Geowissenschaften: FB 09: Chemie, Pharmazie und Geowissenschaftende_DE
opus.subject.otherhexa-peri-hexabenzocoronene, discotic liquid crystal, self-organization, molecular electronic, synthesisen_GB
opus.type.contenttypeDissertationde_DE
opus.type.contenttypeDissertationen_GB

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