ozonide


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Related to ozonide: Ozonolysis

o·zo·nide

(ō'zō-nīd),
The unstable intermediate formed by the reaction of ozone with an unsaturated organic compound, especially with unsaturated fatty acids.
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Microwave Spectrum, Molecular Structure and Dipole Moment of the Primary Ozonide (1,2,3-Trioxolane).
The literature shows that ozone attacks double bonds by formation of unstable ozonides, which lead to the formation of carbonyl groups, preferentially acid groups (33).
Examples include primary and secondary ozonides, peroxyhemiacetals, [alpha]-hydroxy ketones, [alpha]-hydroxy hydroperoxides, and peroxyacyl nitrates (Atkinson and Arey 2003; Docherty et al.
2] with the unsaturation (C=C) in the rubber to form ozonides (ref.
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.