T
T. Oguchi
Researcher at University of Tsukuba
Publications - 4
Citations - 94
T. Oguchi is an academic researcher from University of Tsukuba. The author has contributed to research in topics: Benzyl alcohol & Titanium dioxide. The author has an hindex of 2, co-authored 4 publications receiving 93 citations.
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Semiconductor-catalyzed photooxygenation of aromatic olefins
TL;DR: In this article, a possible mechanism for semiconductors (TiO 2 and CdS) suspended in organic solvents containing 1,1-diphenylethylene and its derivatives under oxygen afforded the corresponding epoxides and benzophenone.
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Titanium dioxide photocatalyzed oxidation of aromatic hydrocarbons: the role of water and oxygen to induce aromatic hydroxylation
TL;DR: In this paper, the effects of oxygen and water on titanium dioxide photocatalyzed oxidation of benzene and toluene were examined, and it was shown that electron transfer from water and benzene to the photogenerated positive holes, synchronized with electron transferred from photoexcited titanium dioxide to oxygen, result in aromatic nuclear hydroxylation giving phenolic products and in oxidation of the side chain of toluenes affording benzyl alcohol and benzaldehyde.
Journal ArticleDOI
Semiconductor-catalyzed Photoreactions of Organic Compounds
Katsumi Tokumaru,Hirochika Sakuragi,Tatsuya Kanno,T. Oguchi,Hiroaki Misawa,Y. Shimamura,Yasunao Kuriyama +6 more
TL;DR: On montre que TiO 2 et CdS induisent loxydation d'olefines et d'hydrocarbures aromatiques, and sensibilisent de systemes insatures.
Journal ArticleDOI
Titanium dioxide photocatalyzed oxidation of aromatic hydrocarbons: the role of water and oxygen to induce aromatic hydroxylation
TL;DR: In this paper, the effects of oxygen and water on titanium dioxide photocatalyzed oxidation of benzene and toluene were examined, and it was shown that electron transfer from water and benzene to the photogenerated positive holes, synchronized with electron transferred from photoexcited titanium dioxide to oxygen, result in aromatic nuclear hydroxylation giving phenolic products and in oxidation of the side chain of toluenes affording benzyl alcohol and benzaldehyde.