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    Electronic spectra and triplet state properties of superphane
    (1986) Schweitzer, Dieter; Hausser, Karl H.; Vogler, Helmut; Staab, Heinz A.; Boekelheide, Virgil
    The emission and the zero-field splitting parameters D and E of the superphane 1 and the [25](1,2,3,4,5)-cyclophane 2 are investigated. The large number of six and five methylene bridges, respectively, leads to a more rigid molecular frame and to a smaller transanular distance as compared to other [2.2]cyclophanes. The experimental results exhibit characteristics features which are due to these unusual properties; they are discussed and compared with semi-empirical Π-electron calculations.
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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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    Transanular interaction in [2.2]phanes: models for dimers?
    (1979) Goldacker, Wilfried; Hausser, Karl H.; Schweitzer, Dieter; Staab, Heinz A.
    The emission spectra of pseudo-ortho 3 and pseudo-geminal-4,7,12,15-tetramethoxy[2.2]-paracyclophane 3 were measured in glass matrices at 1.3 K. Furthermore, the zero field splitting parameters D and E and the decay rate constants ki of the excited triplet state were studied by optical detection of magnetic resonance in zero field. The results were compared with the corresponding monomer 1,4-dimethyl-2,5-dimethoxybenzene.
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    Investigation of the excited triplet states of [2.2]- and [3.3]paracyclophane
    (1979) Melzer, Guenter; Schweitzer, Dieter; Hausser, Karl H.; Colpa, Johannes Pieter; Haenel, Matthias
    We have studied the excited triplet states of [2-2]- and [3.3]paracyclophane by emission spectroscopy and by ODMR and have compared the results with the corresponding monomer paraxylene. The most striking result is that both phanes exhibit two sets of zero field splitting parameters indicating the existence of two nearly degenerate low lying excited triplet states. Furthermore, we find in distinction to expection a stronger reduction of the zero field splitting parameters as compared to the monomers for [3.3]paracyclophane than for [2.2]paracyclophane. The causes of these surprising experimental findings are discussed.
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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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    Electron spin echo determination of spin diffusion in the one-dimensional conductor (fluoranthenyl)2+(PF6)x-(SbF6)1-x-(x ≈ 0.5)
    (1983) Sigg, Jakob; Prisner, Thomas; Dinse, Klaus Peter; Brunner, Hermann; Schweitzer, Dieter; Hausser, Karl H.
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    Spin rotation interaction and anisotropic chemical shift in 13CS2
    (1971) Spiess, Hans Wolfgang; Schweitzer, Dieter; Haeberlen, Ulrich; Hausser, Karl H.
    The 13C nuclear spin-lattice relaxation time T1 was studied in liquid CS2 from -106°C to +35°C at resonance frequencies of 14, 30, and 62 MHz. The relaxation is caused by anisotropic chemical shift and spin-rotation interaction. It is shown that for linear molecules the spin-rotation constant C and the anisotropy of the chemical shift Δσ can be obtained from the relaxation rates without use of adjustable parameters. The analysis yields: C = -13.8 ± 1.4 kHz and Δσ = 438 ± 44 ppm.
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    Overhauser effect experiments on the one-dimensional conductor (perylene)2+PF6-·2/3THF
    (1984) Brunner, Hermann; Hausser, Karl H.; Keller, Heimo J.; Schweitzer, Dieter
    We have measured the Overhauser enhancement of the protons and the 19F-nuclei of the one-dimensional conductor (perylene)2+PF6-·2/3THF in its metallic phase at room temperature. The enhancement factor V was found to be VP=+320±20 for the protons and VF=+175±40 for the 19F-nuclei indicating a predominantly scalar interaction with the conduction electrons in both cases.
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    Transanular interaction in [2.2]phanes: [2.2](2,7)pyrenophane
    (1976) Schweitzer, Dieter; Hausser, Karl H.; Kirrstetter, Reiner G. H.; Staab, Heinz A.
    The emission spectra of [2.2](2,7)pyrenophane and the zero field splitting parameters D and E of its excited triplet state were measured in glasses and in small single crystals at 1.3 K. The results are being compared with monomer pyrene and 2,7 dimethylpyrene in liquid and solid solutions as well as in single crystals.
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    Transannular interactions in [2.2] phanes as studied by magnetic resonance and optical spectra
    (1975) Schweitzer, Dieter; Colpa, Johannes Pieter; Behnke, J.; Hausser, Karl H.; Haenel, Matthias; Staab, Heinz A.
    The interaction of π-electrons in [2.2] phanes was studied both experimentally and theoretically. The fluorescence and phosphorescence spectra were measured at liquid helium temperature; in addition, the zero field splitting parameters D and E were determined by ODMR in zero field and by ordinary ESR at X-band. The results for the phanes with two identical aromatic units can be summarized as follows: The rather small reduction of the D and E values of the order of 10% with respect to the monomers indicates, in agreement with the theoretical treatment given in part II, that the two unpaired electrons of the excited triplet state have a high probability to be at a given time in the same half of the molecule. While the fluorescence spectra show the typical behaviour of emission spectra of dimers or excimers, the phosphorescence spectra exhibit some remaining structure. This behaviour which indicates a somewhat weaker coupling among the triplet orbitals as compared to the singlet orbitals can also be understood on the basis of theoretical considerations. For a phane with two different aromatic units the behaviour is found to be more similar to the corresponding aromatic monomer with the lower excited states with some perturbation by the other part of the phase also in agreement with theoretical expectation.