Liquid-phase autooxidation of retinyl polyenes
β Scribed by E. I. Finkelshtein; Yu. M. Rubchinskaya; E. I. Kozlov
- Book ID
- 102445270
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 454 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0538-8066
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β¦ Synopsis
The autooxidation of retinyl acetate and methyl retinoate was investigated in chlorobenzene at 45Β°C. The rates of thermal initiation in the retinyl acetate solutions were measured, and a value was determined of the rate constant for the reaction of oxygen with retinyl acetate (RH + 0, + R.
The number of moles of oxygen absorbed per mole of polyene depends on the substrate concentration. A kinetic scheme for the methyl retinoate autooxidation was proposed which takes into account the isomerization of primary peroxy radicals, and the rate constants for different elementary reactions were estimated. The partial rate constant for "allylic" hydrogen abstraction from retinyl acetate was estimated to be 3 1.65 x lo3 L/mol . s. A probable propagation sequence was proposed for the autooxidation of retinyl acetate.
π SIMILAR VOLUMES
The autooxidation of methyl-and dimethyl-substituted N-, S-, and O-heterocyclic compound derivatives has been studied in 1,2-dimethoxyethane--t-BuOK in the presence of l8-crown-6. Monoand dicarboxylic acid derivatives of pyrazine, pyridine, pyrimidine, and thiophene have been synthesized. Autooxida