| Literature DB >> 17256946 |
Axel G Griesbeck1, Miyeon Cho.
Abstract
The visible-light irradiation of 9-mesityl-10-methylacridinium perchlorate 1 in the presence of monoalkenes and molecular oxygen leads to typical products of singlet oxygen addition (type II photooxygenation). The molecular probes 1-methylcyclohexene and limonene, respectively, result in hydroperoxide mixtures with a characteristic product pattern. A switch in the oxidative mechanism (electron-transfer photooxygenation) is observed for naphthalene derivatives as electron-rich acceptor molecules, revealing that the 9-mesityl-10-methylacridinium cation serves as a dual sensitizer with the capacity of efficient singlet oxygen formation and electron-transfer reaction. [reaction: see text].Entities:
Year: 2007 PMID: 17256946 DOI: 10.1021/ol0628661
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005