A physical study of the degradation of periodate–oxidized amylose
✍ Scribed by Stig R. Erlander; H. L. Griffin; F. R. Senti
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1964
- Tongue
- English
- Weight
- 469 KB
- Volume
- 2
- Category
- Article
- ISSN
- 0006-3525
No coin nor oath required. For personal study only.
✦ Synopsis
Changes in the viscosity of amylose that had been oxidized in an aqueous medium a t p H 3.0 by sodium metaperiodate were followed aa a function of time. Levels of 20, 40, 60,80, and 100% periodate oxidation were attained. The rate of hydroxyl ion cleavage of the periodate-oxidized amylose [d( l/[q]Z)/dt = k] is proportional to the square of the degree of oxidation. That is, the hydroxyl ion hydrolysis of periodate oxyamylose occurs predominately a t the site where two or more oxidized units exist side by side. A reaction mechanism is postulated to account for this slow breakdown of an isolated oxidized unit and for the fast degradation of two adjacent oxidized glucose units. When two or more oxidized units exist side by side, the free aldehyde a t carbon atom 3 is believed to be in equilibrium with a hydrate instead of a hemiacetal structure as in the case of a single, isolated, oxyglucose unit in amylose. The greater reversibility of the hydrate to the free aldehyde structure results in a greater possibility of 6-alkoxycarbonyl elimination a t sites where two or more oxidized glucose units exist side by side.
📜 SIMILAR VOLUMES
The kinetic parameters for the dissociation of the amylose-1-␣-lysophosphatidilcholine complex were studied by differential scanning calorimetry, using the Borchardt-Daniels and dynamic methods. The reaction order was found to be close to 1 with an activation energy of 419 kJ/mol and the results wer
The iron(II) complex of H 2 L 14-dimethyl-4, 7, 10, 13-tetraazahexadeca-(H L ϭ 3, 2 3,13-diene-2,15-dione dioxime, Coord. Chem. Rev., 33, 87 (1980)) is oxidized by periodate very rapidly in the range pH 2.0-7.0, and the kinetics of the reaction has been followed by stoppedflow spectrophotometry at 3