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Liquid-phase autooxidation of retinyl polyenes

✍ 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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✦ 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.


πŸ“œ SIMILAR VOLUMES


Autooxidation of methylheterocycles unde
✍ I. G. Iovel'; Yu. Sh. Gol'dberg; A. P. Gaukhman; R. M. Zolotoyabko; M. V. Shiman πŸ“‚ Article πŸ“… 1991 πŸ› Springer US 🌐 English βš– 312 KB

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