08 Fakultät Mathematik und Physik

Permanent URI for this collectionhttps://elib.uni-stuttgart.de/handle/11682/9

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Author: search.filters.author.Effenberger, FranzSubject: search.filters.subject.530

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    Intramolecular energy transfer through linear polyenes : effect of spacers
    (1990) Blessing, Gerd; Holl, Norbert; Port, Helmut; Wolf, Hans Christoph; Effenberger, Franz; Kesmarszky, Thomas; Schlosser, Hubert
    The optical properties of linear polyenes terminally substituted with different molecules (mainly anthryl- and TPP-substituents) have been studied. Bicyclic spacers within the polyene chain affect the quantum yields but do not interrupt intramolecular energy transfer between the endgroups.
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    Dual fluorescence of 9-anthryl-substituted oligothiophenes in nonpolar environment
    (1994) Emele, Peter; Meyer, Dirk U.; Holl, Norbert; Port, Helmut; Wolf, Hans Christoph; Würthner, Frank; Bäuerle, Peter; Effenberger, Franz
    9-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.
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    Fulgides as switches for intramolecular energy transfer
    (1993) Walz, Jochen; Ulrich, Karl; Port, Helmut; Wolf, Hans Christoph; Wonner, Johann; Effenberger, Franz
    In a molecular unit which is a donor-fulgimide-acceptor triade, the possibility of an intramolecular energy transfer from donor to acceptor depends upon the isomer configuration of the photochromic fulgimide. It is shown that a switching on and off of this intramolecular energy transfer is possible by photoinduced shifting of the fulgimide levels between a trap and an antitrap function.