THE ROLE OF A TRIPLET STATE IN THE PHOTOREDUCTION OF BENZOPHENONE
โ Scribed by Hammond, George S.; Moore, William M.
- Book ID
- 126810980
- Publisher
- American Chemical Society
- Year
- 1959
- Tongue
- English
- Weight
- 149 KB
- Volume
- 81
- Category
- Article
- ISSN
- 0002-7863
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๐ SIMILAR VOLUMES
The reaction of triplet benzophenone with the tertiary amines triisopropylamine and diisopropyl-3-pentylami~e does not lead to photoreduction. An explanation of this unusual behaviour is given based on the particular structure of these amines. The initial charge transfer events are compared with tho
Although it has been unambigously established that the lowest triplet state of benzophenone and many of its derivatives [2,3] is a 3(n, z\*) [l],
Ring atom hypcrfine structure hus been observed in the optically-detected ms,Pnetic resonance (ODMH) spectra of the lows: triplet states of 4,4'-difluoro-and 4,4'dibromobenzop~lenone in a single crystal host at liquid helium temperatures. An an~~lysis of this structurt! 2nd its angular dependence yi