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dc.contributor.authorEmele, Peterde
dc.contributor.authorMeyer, Dirk U.de
dc.contributor.authorHoll, Norbertde
dc.contributor.authorPort, Helmutde
dc.contributor.authorWolf, Hans Christophde
dc.contributor.authorWürthner, Frankde
dc.contributor.authorBäuerle, Peterde
dc.contributor.authorEffenberger, Franzde
dc.date.accessioned2009-08-28de
dc.date.accessioned2016-03-31T08:35:47Z-
dc.date.available2009-08-28de
dc.date.available2016-03-31T08:35:47Z-
dc.date.issued1994de
dc.identifier.other316281182de
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:bsz:93-opus-44588de
dc.identifier.urihttp://elib.uni-stuttgart.de/handle/11682/4881-
dc.identifier.urihttp://dx.doi.org/10.18419/opus-4864-
dc.description.abstract9-Anthryl-oligothiophenes (9A-Tn, n = 1–4) have been studied in n-hexane solution between helium and room temperature using absorption, fluorescence emission and excitation spectra and time resolved fluorescence measurements. These compounds are reference systems for studies on intramolecular energy and charge transfer in donor/acceptor-substituted conjugated chain molecules. The absorption spectra show contribution of both substituents anthracene and oligothiophene, but no additional bands due to mixed electronic states. Dual fluorescence is observed at Tgreater-or-equal, slanted 120 K for the compounds 9A-Tn (n = 1–3), but not for 9A-T4. Time resolved spectroscopy reveals a dynamical coupling between the two emission components whose relative quantum yields are strongly temperature dependent. The occurrence of the dual fluorescence is explained by an intramolecular torsional motion between the two molecular subunits.en
dc.language.isoende
dc.rightsinfo:eu-repo/semantics/openAccessde
dc.subject.classificationOligothiophene , Energietransport <Mikrophysik> , Fluoreszenz , Absorptionde
dc.subject.ddc530de
dc.titleDual fluorescence of 9-anthryl-substituted oligothiophenes in nonpolar environmenten
dc.typearticlede
ubs.fakultaetFakultät Mathematik und Physikde
ubs.fakultaetFakultät Chemiede
ubs.institut3. Physikalisches Institutde
ubs.institutInstitut für Organische Chemiede
ubs.opusid4458de
ubs.publikation.sourceChemical Physics 181 (1994), S. 417-424. URL http://dx.doi.org./10.1016/0301-0104(94)00007-7de
ubs.publikation.typZeitschriftenartikelde
Enthalten in den Sammlungen:08 Fakultät Mathematik und Physik

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