Generation-dependent energy dissipation in rigid dendrimers studied by 
femtosecond to nanosecond time-resolved fluorescence spectroscopy

Lor, M.; De, R.; Jordens, S.; De Belder, G.; Schweitzer, G.; Cotlet, M.; Hofkens, J.; Weil, T.; Herrmann, A.; Müllen, Klaus; Van der Auweraer, M.; De Schryver, F. C.

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Generation-dependent energy dissipation in rigid dendrimers studied by femtosecond to nanosecond time-resolved fluorescence spectroscopy

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Weil, T.
MPI for Polymer Research, Max Planck Society;

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Herrmann, A.
MPI for Polymer Research, Max Planck Society;

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Müllen, Klaus
MPI for Polymer Research, Max Planck Society;

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引用

Lor, M., De, R., Jordens, S., De Belder, G., Schweitzer, G., Cotlet, M., Hofkens, J., Weil, T., Herrmann, A., Müllen, K., Van der Auweraer, M., & De Schryver, F. C. (2002). Generation-dependent energy dissipation in rigid dendrimers studied by femtosecond to nanosecond time-resolved fluorescence spectroscopy. Journal of Physical Chemistry A, 106(10), 2083-2090.

引用: https://hdl.handle.net/11858/00-001M-0000-000F-6662-9

要旨

Intramolecular kinetic processes in a series of second- generation polyphenyl dendrimers with multiple peryleneimide chromophores attached to the para position of the outer phenyl ring were investigated by steady-state and femtosecond to nanosecond time-resolved fluorescence spectroscopy. The results obtained were compared to the ones of the corresponding first- generation dendrimer series. The energy-hopping rate constant, k(hopp), observed from anisotropy decay times was found to be 5 times smaller than that of the first-generation series and scales well with the difference in average distance between the chromophores. In addition to the processes observed in first- generation dendrimers in the ultrafast time domain by fluorescence up-conversion, a second. annihilation process is found in the second-generation multichromophoric dendrimer. The observation of two singlet-singlet annihilation processes in this compound can be explained by the presence of a mixture of constitutional isomers leading to a broader distribution of distances between neighboring chromophores compared to first- generation multichromophoric dendrimers.