The lead tetraacetate (LTA) oxidation of saturated alcohols in non-polar solvents affords usually as major products unsubstituted tetrahydrofuran-type ethers, the formation of which involves intramolecular 1,5-hydrogen abstraction by the initially produced alkoxy radicals, followed by internal attac
The reaction of sulphur and sulphur compounds with olefinic substances. Part VI. Factors influencing cyclic sulphide formation in the reaction of sulphur with polyisoprenes
✍ Scribed by Bloomneld, George F.
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1949
- Weight
- 364 KB
- Volume
- 68
- Category
- Article
- ISSN
- 0368-4075
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✦ Synopsis
SULPHIDE FORMATION IN THE REACTION OF SULPHUR WITH POLYISOPRENES
PART vr. FACTORS INFLUENCING CYCLIC
By GEORGE F. BLOOMNELD
Cyclic sulphidcs arc to a large extent secondary products of the reamon of primarily-formcd intermolecular polysulphides with polyisoprene hydrocarbon, and undue prolongation of the time of reaction of sulphur with polyisoprcnes favours cyclic sulphide formation and so reduces the cross-linking efficiency of the sulphur. Various accclcrating substances markedly increase thc cross-linking efficiency either by permitting shorter reaction times to be employed, ting 3 cross-linking nthcr than a cyclizing reaction of the ~~~~~. o ~h i u n m disulphide accelerators in the absence of sulphur bring about cross-1 ng, the linkages being of C-S-C type rather than C -C . 9
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