Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-5974
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dc.contributor.authorTober, Natalie-
dc.contributor.authorWinter, Johannes-
dc.contributor.authorJochem, Matthias-
dc.contributor.authorLehmann, Matthias-
dc.contributor.authorDetert, Heiner-
dc.date.accessioned2021-06-22T07:54:11Z-
dc.date.available2021-06-22T07:54:11Z-
dc.date.issued2021-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/5983-
dc.description.abstractC3-symmetrical, alkoxyphenyl substituted 2,5,8-(tris-1,3,4-oxadiazol-2-yl)benzo [1,2-b; 3,4-b′; 5,6-b′′]trithiophenes (OXD-BTT) are synthesized via threefold Huisgen-reaction. A broad variation of alkoxy substitution pattern and chain lengths is reported. The thermal behavior was investigated via differential scanning calorimetry (DSC), polarized optical microscopy (POM) and thermogravimetry (TGA). Optical properties were studied via UV-Vis and fluorescence spectroscopy. Structural information of the LC phases was gained from X-ray diffraction on oriented fibers. OXD-BTT provide enormous phase widths (ΔT≥289 K) with clearing points close to thermal decomposition. Most of the derivatives exhibit two different mesophases, the lower phase with a rectangular 3D-structure and a hexagonal 2D-lattice at higher temperature. The variation of the chain length allows a tuning of melting and clearing points. OXD-BTT emit blue light with fluorescence quantum yields up to 30 % in good solvents. The emission is very sensitive to aggregation, thus, in poor solvents the emission intensity decreases, and red shift of maxima occurs.en_GB
dc.language.isoengde
dc.rightsCC BY-NC-ND*
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.ddc540 Chemiede_DE
dc.subject.ddc540 Chemistry and allied sciencesen_GB
dc.titleTris(5-aryl-1,3,4-oxadiazolyl)benzotrithiophenes : discotic liquid crystals with enormous mesophase rangesen_GB
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-5974-
jgu.type.dinitypearticleen_GB
jgu.type.versionPublished versionde
jgu.type.resourceTextde
jgu.organisation.departmentFB 09 Chemie, Pharmazie u. Geowissensch.de
jgu.organisation.number7950-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.journal.titleEuropean journal of organic chemistryde
jgu.journal.volume2021de
jgu.journal.issue5de
jgu.pages.start798de
jgu.pages.end809de
jgu.publisher.year2021-
jgu.publisher.nameWiley-VCH Verl.de
jgu.publisher.placeWeinheimde
jgu.publisher.urihttps://doi.org/10.1002/ejoc.202001475de
jgu.publisher.issn1099-0690de
jgu.organisation.placeMainz-
jgu.subject.ddccode540de
jgu.publisher.doi10.1002/ejoc.202001475
jgu.organisation.rorhttps://ror.org/023b0x485
Appears in collections:JGU-Publikationen

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