Energy- and Electron-Transfer Pathways in the Triplet-Sensitized Photolysis ofN-(1-Naphthoyl)-O-(p-toluoyl)-N-phenylhydroxylamine with Substituted Benzophenones
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/65/7/65_7_1950/_pdf
Reference38 articles.
1. Mechanism of the Pyrene-Sensitized Photolysis ofN-(1-Naphthoyl)-O-(p-toluoyl)-N-phenylhydroxylainine
2. Mechanism of the Direct and Triplet-sensitized Photolysis ofN-(1-Naphthoyl)-O-(p-toluoyl)-N-phenylhydroxylamine
3. A new sensitive chemical actinometer - II. Potassium ferrioxalate as a standard chemical actinometer
4. The Photolysis ofN,O-Diacyl-N-phenylhydroxylamines
5. Kinetics of Fluorescence Quenching by Electron and H-Atom Transfer
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1. Formation of Isoquinoline and 1-Azetine Derivatives via Novel Photocyclization of Substituted α-Dehydrophenylalanines;Tetrahedron;2000-05
2. Mechanism of the Benzophenone-Sensitized Photolysis ofO-Benzoyl-N-(1-naphthoyl)-N-phenylhydroxylamine in Cationic Micellar Media;Bulletin of the Chemical Society of Japan;1999-12
3. Anionic Micellar Effects on the Benzophenone-sensitized Photolysis of N-(1-Naphthoyl)-N-phenyl-O-benzoylhydroxylamine;Journal of Chemical Research;1999-11
4. Anionic Micellar Effects on the Benzophenone-sensitized Photolysis of N-(1-Naphthoyl)-N-phenyl-O-benzoylhydroxylamine;Journal of Chemical Research;1999
5. Onium Butyltriphenylborates as Donor−Acceptor Initiators for Sensitized Photopolymerizations of Vinyl Monomer;Macromolecules;1998-08-15
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