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Transannular interactions in [2,2] phanes as studied by magnetic resonance and optical spectra

MPG-Autoren
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Schweitzer,  Dieter
Department of Molecular Physics, Max Planck Institute for Medical Research, Max Planck Society;

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Behnke,  J.
Max Planck Institute for Medical Research, Max Planck Society;

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Hausser,  Karl H.
Department of Molecular Physics, Max Planck Institute for Medical Research, Max Planck Society;

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Haenel,  Matthias
Research Group Haenel, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Staab,  Heinz A.
Department of Organic Chemistry, Max Planck Institute for Medical Research, Max Planck Society;

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Zitation

Schweitzer, D., Colpa, J. P., Behnke, J., Hausser, K. H., Haenel, M., & Staab, H. A. (1975). Transannular interactions in [2,2] phanes as studied by magnetic resonance and optical spectra. Chemical Physics, 11(3), 373-384. doi:10.1016/0301-0104(75)80056-5.


Zitierlink: https://hdl.handle.net/11858/00-001M-0000-002E-031E-D
Zusammenfassung
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.