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Electron-transfer photochemistry of di-tert-butyl nitroxide

✍ Scribed by Anderson, David Richard; Keute, Joseph S.; Chapel, Harold L.; Koch, Tad H.


Book ID
126930870
Publisher
American Chemical Society
Year
1979
Tongue
English
Weight
392 KB
Volume
101
Category
Article
ISSN
0002-7863

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Upper excited state photochemistry of di
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Over the past decade the parsmagnetic compound di-tert-butyl nitroxide (DTBN, 1,) has proved to be an interesting and surprisingly versatile quencher of electronically excited species.

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Di-tert-butyl nitroxide (DTBN) decomposes in aqueous solutions producing 2-methyl-2-nitroso propane (MNP) and tert-butanol. The process is acid catalyzed, it is of second order in DTBN, and takes place with a rate constant of (1.0 2 0.1) M-\* s-'. The reaction is also catalyzed by the anionic surfac