Abstract

Abstract Photoinduced electron-transfer processes between C60/C70 and tetrathienylethylenes (TTE’s) in benzonitrile have been studied by measuring the transient absorption spectra in the Vis/NIR regions using nanosecond laser photolysis. The absorption bands of the radical anions of C60/C70 (C60•−/C70•−) and radical cations of TTE’s (TTE’s•+) were observed with the decay of the triplet states of C60/C70 (3C60*/3C70*), indicating that electron transfer takes place via 3C60*/3C70*. In addition, formation of the dication of TTE (TTE2+) was confirmed by its characteristic absorption band at 680 nm. The TTE2+ is formed by the stepwise collision of TTE with 3C60*/3C70*. By the substitutions with the MeS groups at the thienyl rings of TTE, the efficiencies and rates of the electron-transfer processes became higher than those of TTE with the PhS groups. For dendrimer TTE’s, the photoinduced electron-transfer processes also took place via 3C60*/3C70*, although the efficiencies and rates were decreased with an increase in the dendrimer generation. After forward electron transfer, the back electron transfer processes were observed between separately solvated C60•−/C70•− and TTE’s•+ even for the dendrimer TTE’s, which suggest that outer-sphere back electron-transfer took place in the backward processes.

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