Issue 10, 1991

Photo-induced electron-transfer reaction of naphthalocyanine

Abstract

Quenching of fluorescence emission of a series of siloxanes (R3SiO)2 SiNc by a variety of quenchers ranging from acceptors to donors was studied in dichloromethane solution. The relationship between fluorescence quenching rates and half-wave potentials of the quenchers suggests that quenching results from the photoinduced electron-transfer reaction of substrates (R3SiO)2SiNc with quenchers. The results indicate that (R3SiO)2SiNc acts as an electron-donating sensitizer for acceptors and as an electron-accepting sensitizer for donors. The small values of the Coulombic attraction (ωp) obtained from our experiments indicate that the radical-ion pair consisting of (R3SiO)2SiNc and a quencher can dissociate easily even in dichloromethane, because (R3SiO)2SiNc is an extremely large molecule.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1991, 1637-1641

Photo-induced electron-transfer reaction of naphthalocyanine

S. Tai, S. Hayashida and N. Hayashi, J. Chem. Soc., Perkin Trans. 2, 1991, 1637 DOI: 10.1039/P29910001637

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