Photoinduced electron-transfer carbon-carbon bond cleavage of radical cations of carbonyl compounds in solution. 2, 4, 6-Triphenylpyrylium salt-sensitized …

…, M Kamata, H Sakuragi, K Tokumaru

Index: Akaba, Ryoichi; Niimura, Yuji; Fukushima, Takao; Kawai, Yukinori; Tajima, Tomonori; Kuragami, Toshiko; Negishi, Akio; Kamata, Masaki; Sakuragi, Hirochika; Tokumaru, Katsumi Journal of the American Chemical Society, 1992 , vol. 114, # 12 p. 4460 - 4464

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Citation Number: 31

Abstract

Abstract Photosensitized electron transfer oxygenation of several aralkyl ketones and aldehydes such as 1, 2, 2-triphenylethanone and diphenyl-and triphenylethanal has been carried out with 2, 4, 6-triphenylpyrylium tetrafluoroborate (TPP+ BF4-) in dichloromethane. The carbonyl compounds underwent CC bond cleavage through their cation radicals, generated via electron transfer to the excited singlet state of the pyrylium salt. For example ...

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