Photochemical Oxidation of Thioketones by Singlet Molecular Oxygen Revisited: Insights into Photoproducts, Kinetics, and Reaction Mechanism

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• 作者：Antonio J. S谩nchez-Arroyo ; Zulay D. Pardo ; Florencio Moreno-Jim茅nez ; Antonio Herrera ; Nazario Mart铆n ; David Garc铆a-Fresnadillo
• 刊名：Journal of Organic Chemistry
• 出版年：2015
• 出版时间：November 6, 2015
• 年：2015
• 卷：80
• 期：21
• 页码：10575-10584
• 全文大小：467K
• ISSN：1520-6904

文摘

Photosensitized oxidation of trimethyl[2.2.1]bicycloheptane thioketones by ¹O₂ can yield more photoproducts than exclusively ketones and sulfines. Moreover, the ketone/sulfine ratio can be reversed when protic conditions and high thioketone concentrations are used, conversely to earlier results reporting ketones as the main photoproducts. A new mechanistic proposal for sulfine formation is suggested following intermolecular oxygen transfer from a peroxythiocarbonyl intermediate to a second thioketone molecule. Reaction quantum yields (10^鈥?鈥?0^鈥?) depend on the reaction conditions and time. Sulfine production reaches a maximum at short irradiation times, whereas decomposition to the corresponding ketone is observed at long reaction times. When the thioketone substrate has a hydrogen atom at the 伪 position a peroxyvinylsulfenic acid intermediate can be formed by proton transfer. Reaction of this intermediate with another thioketone molecule can yield more sulfine and its tautomeric vinylsulfenic acid, which dimerizes in situ to the thiosulfinate. The hydroperoxyl group of the peroxyvinylsulfenic acid can also rearrange to the 伪 position, and by reaction with the starting thioketone, 伪-hydroxy thioketone and additional sulfine can be formed, while dehydration yields the 伪-oxo thioketone. In situ [2 + 2] and [4 + 2] self-cycloaddition of the 伪-oxo thioketone yields significant amounts of the corresponding adducts at prolonged irradiation times.