TY  - JOUR
A1  - Schwarze, Thomas
A1  - Mueller, Holger
A1  - Dosche, Carsten
A1  - Klamroth, Tillmann
A1  - Mickler, Wulfhard
A1  - Kelling, Alexandra
T1  - Luminescence detection of open-shell transition-metal ions by photoinduced electron transfer controlled by internal charge transfer of a receptor
Y1  - 2007
UR  - http://onlinelibrary.wiley.com/doi/10.1002/ange.200603992/pdf
U6  - https://doi.org/10.1002/anie.200603992
ER  - 
TY  - GEN
A1  - Dosche, Carsten
A1  - Mickler, Wulfhard
A1  - Löhmannsröben, Hans-Gerd
A1  - Agenet, Nicolas
A1  - Vollhardt, K. Peter C.
T1  - Photoinduced electron transfer in [N]phenylenes
N2  - First studies of electron transfer in [N]phenylenes were performed in bimolecular quenching reactions of angular [3]- and triangular [4]phenylene with various electron acceptors. The relation between the quenching rate constants kq and the free energy change of the electron transfer (ΔG0CS ) could be described by the Rehm-Weller equation. From the experimental results, a reorganization energy λ of 0.7 eV was derived. Intramolecular electron transfer reactions were studied in an [N]phenylene bichomophore and a corresponding reference compound. Fluorescence lifetime and quantum yield of the bichromophor display a characteristic dependence on the solvent polarity, whereas the corresponding values of the reference compound remain constant. From the results, a nearly isoenergonic ΔG0CS can be determined. As the triplet quantum yield is nearly independent of the polarity, charge recombination leads to the population of the triplet state.
T3  - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 23 
KW  - [N]phenylenes
KW  - photoinduced electron transfer
KW  - [N]phenylene dyads
Y1  - 2007
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus-12463
ER  - 
TY  - JOUR
A1  - Dosche, Carsten
A1  - Mickler, Wulfhard
A1  - Löhmannsröben, Hans-Gerd
A1  - Agenet, Nicolas
A1  - Vollhardt, K. Peter C.
T1  - Photoinduced electron transfer in [N]phenylenes
N2  - First studies of electron transfer in [N]phenylenes were performed in bimolecular quenching reactions of angular [3]- and triangular [4]phenylene with various electron acceptors. The relation between the quenching rate constants k(q) and the free energy change of the electron transfer (Delta G(CS)(0)) could be described by the Rehm- Weller equation. From the experimental results, a reorganization energy lambda of 0.7 eV was derived. Intramolecular electron transfer reactions were studied in an [N]phenylene bichomophore and a corresponding reference compound. Fluorescence lifetime and quantum yield of the bichromophor display a characteristic dependence on the solvent polarity, whereas the corresponding values of the reference compound remain constant. From the results, a nearly isoenergonic charge separation process can be determined. As the triplet quantum yield is nearly independent of the polarity, charge recombination leads to the population of the triplet state.
Y1  - 2007
UR  - http://www.sciencedirect.com/science/journal/10106030
U6  - https://doi.org/10.1016/j.jphotochem.2006.12.038
SN  - 1010-6030
ER  -