Universität Stuttgart

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    Optical detection of magnetic resonance (ODMR) of triple-layered phanes
    (1981) Melzer, Guenter; Schweitzer, Dieter; Hausser, Karl H.; Staab, Heinz A.; Zapf, Udo
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    Spectroscopic properties of kekulene
    (1981) Schweitzer, Dieter; Hausser, Karl H.; Diederich, Francois; Staab, Heinz A.; Vogler, Helmut
    Kekulene [1,2] is the first example of a new class of aromatic compounds in which the annelation of six membered rings leads to a cyclic system enclosing a cavity with hydrogen atoms.
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    Optical detection of magnetic resonance (ODMR) of naphthalenophanes
    (1981) Schweitzer, Dieter; Hausser, Karl H.; Blank, Norman E.; Haenel, Matthias
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    ZFS-tensor of the triplet states of [2.2]phanes as studied by ESR
    (1981) Bär, Monika; Dinse, Klaus Peter; Goldacker, Wilfried; Hausser, Karl H.; Schweitzer, Dieter; Zimmermann, Herbert; Krieger, Claus
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    Influence of an identified dimer vibration on the emission spectrum of [2,2]paracyclophane
    (1980) Goldacker, Wilfried; Schweitzer, Dieter; Dinse, Klaus Peter; Hausser, Karl H.
    The emission spectrum of polycrystalline [2,2]paracylophane shows a resolved vibronic structure with a 241 cm−1 progression at He temperatures. The dependence of the energy of this mode upon selective deuteration in combination with results from FIR and Raman spectra could be used to identify the mode as a torsional dimer vibration. The emission spectra could be simulated assuming a linear coupling of the torsional mode to the electronic transitions with coupling strengths of S = 10 (fluorescence) and S = 13 (phosphorescence). This corresponds to an equilibrium displacement of the benzene rings under electronic excitation by a torsional angle of 10.6° (S1) and 12.1° (T1), in addition to the small torsion in the ground state S0 by about 3°.