Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
28894 | Journal of Photochemistry and Photobiology A: Chemistry | 2007 | 4 Pages |
Abstract
Photolysis of 2,5-dichloro-3,6-bis(dialkylamino)-[1,4]benzoquinone (1) at 254 nm or 300–500 nm produces the corresponding cyclized products (2) via the electron transfer-proton transfer sequence in a variety of solvents in quantitative yields within 10 min. In contrast, photolysis of 2,5-dichloro-3,6-bis(dialkylamino)-[1,4]benzoquinone (1) at >500 nm light source affords the elimination products (3) in good yields via the δ-hydrogen abstraction.
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Physical Sciences and Engineering
Chemical Engineering
Bioengineering
Authors
Min Shi, Wang-Gui Yang, Shuai Wu,