TY - JOUR
T1 - Photoinduced intramolecular electron-transfer reactions in carbazole-fullerene and phenothiazine-fullerene linked compounds in benzene and benzonitrile as studied by fluorescence, transient absorption, time-resolved EPR, and magnetic field effects
AU - Yonemura, Hiroaki
AU - Moribe, S.
AU - Hayashi, K.
AU - Noda, M.
AU - Tokudome, H.
AU - Yamada, S.
AU - Nakamura, H.
PY - 2003
Y1 - 2003
N2 - Photoinduced intramolecular electron-transfer reactions in carbazole (Cz)-fullerene (C60) (Cz(8)C60) and phenothiazine (Ph)-C60 (Ph(n)C60 (n = 8, 10, 12)) linked compounds have been investigated in benzene and benzonitrile by fluorescence, transient absorption, and time-resolved electron paramagnetic resonance measurements, and by magnetic field effects on the decay rate constants of the photogenerated biradicals. In benzonitrile, photoinduced intramolecular electron transfer from Cz to the singlet excited state of C60 (1C60*) occurred in Cz(8)C60, but not to the triplet excited state (3C60*), while the intramolecular electron-transfer to both 1C60* and 3C60* occurred in Ph(n)C60 (n = 8, 10, 12). In benzene, on the other hand, no electron transfer to both 1C60* and 3C60* took place in all linked compounds. These results were interpreted in terms of the different Gibbs free energy changes in the two solvents.
AB - Photoinduced intramolecular electron-transfer reactions in carbazole (Cz)-fullerene (C60) (Cz(8)C60) and phenothiazine (Ph)-C60 (Ph(n)C60 (n = 8, 10, 12)) linked compounds have been investigated in benzene and benzonitrile by fluorescence, transient absorption, and time-resolved electron paramagnetic resonance measurements, and by magnetic field effects on the decay rate constants of the photogenerated biradicals. In benzonitrile, photoinduced intramolecular electron transfer from Cz to the singlet excited state of C60 (1C60*) occurred in Cz(8)C60, but not to the triplet excited state (3C60*), while the intramolecular electron-transfer to both 1C60* and 3C60* occurred in Ph(n)C60 (n = 8, 10, 12). In benzene, on the other hand, no electron transfer to both 1C60* and 3C60* took place in all linked compounds. These results were interpreted in terms of the different Gibbs free energy changes in the two solvents.
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U2 - 10.1007/BF03166622
DO - 10.1007/BF03166622
M3 - Article
AN - SCOPUS:0037266439
SN - 0937-9347
VL - 23
SP - 289
EP - 307
JO - Applied Magnetic Resonance
JF - Applied Magnetic Resonance
IS - 3-4
ER -