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The unstable intermediate formed by the reaction of ozone with an unsaturated organic compound, especially with unsaturated fatty acids.
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Alcohols, carbonyls, and carboxylic acids enhance the formation of secondary ozonides, as well as alkoxy and acyloxy hydroperoxides, from stabilized Criegee intermediates formed in [O.
without any tension and extension of the vulcanizate, the ozone attacks only the double bonds on the surface of the elastomer where ozonides are formed, the absorption being restricted to the surface layers.
Reactions of alkenes with ozone in the gas phase: a matrix-isolation study of secondary ozonides and carbonyl-containing reaction products.