Intramolecular relaxation of phenyl-alkyl ketones
β Scribed by M.A. Mazid; S. Walker; N.A. Weir
- Publisher
- Elsevier Science
- Year
- 1981
- Weight
- 552 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0378-4487
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β¦ Synopsis
Dielectric absorption studies have been made (with one exception) in the ranges ED-280K and IO*-IO5 Hz of eight ketones of the type C6H5COR where R is varied from CH3 to C10H2, in a polystyrene matrix. An intramolecular relaxation process has been found in each case with an enthalpy of activation of the same order of magnitude as that for acetyl group relaxation in acetophenone, 4-acetylbiphenyl and 1,4-diacetylbenzene. Feasible intramolecular relaxation processes have been considered.
π SIMILAR VOLUMES
Several phenyl alkyl ketones display two overlapping short-lived pilosphorescenccs at 77"K, with O-O bands at 384 nm (74.5 kcal) and 397 nm (72.0 kcal). The hgher energy emission (T = S-10 msec) is favored in rigid methylcyclohesane glasses, while the proportion of lowcr-encrgy emission (T = 4-5 mse
## Abstract The CH adducts of benzaldehyde, acetophenone, propiophenone and butyrophenone were prepared using CH~3~Fο£ΏCH~4~ and CH~3~Clο£ΏCH~4~ mixtures under chemical ionization conditions and the unimolecular and collisionβinduced fragmentation reactions of their adduct ions were studied. For compar