Difference between revisions of "Ozonide"

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(New page: __NOTOC__ {{Editor Help}} '''Ozonide''' is an unstable, reactive polyatomic anion O<sub>3</sub><sup>−</sup>, derived from ozone, or an organic compound si...)
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* [[peroxide]], O<sub>2</sub><sup>2&minus;</sup>
* [[peroxide]], O<sub>2</sub><sup>2&minus;</sup>
* [[oxide]], O<sup>2&minus;</sup>
* [[oxide]], O<sup>2&minus;</sup>
* [[dioxygenyl]], O<sub>2</sub><sup>+</sup>
* dioxygenyl, O<sub>2</sub><sup>+</sup>

Revision as of 15:23, 13 February 2008

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Ozonide is an unstable, reactive polyatomic anion O3, derived from ozone, or an organic compound similar to organic peroxide formed by a reaction of ozone with an unsaturated compound.

Inorganic ozonides

Inorganic ozonides are dark red ionic compounds containing the reactive O3 anion. The anion has the V shape of the ozone molecule.

Inorganic ozonides are formed by burning potassium or heavier alkali metals in ozone, or by treating the alkali metal hydroxide with ozone; if potassium is left undisturbed in air for years it accumulates a covering of superoxide and ozonide. They are very sensitive explosives that have to be handled at low temperatures in an atmosphere comprised of an inert gas. Lithium and sodium ozonide are extremely unstable and must be prepared by low-temperature ion exchange starting from CsO3, and the pure solids cannot be isolated.

Inorganic ozonides are being investigated as promising sources of oxygen in chemical oxygen generators.

Organic ozonides

Organic ozonides are more explosive cousins of the organic peroxides and contain a covalently bonded ozonide group, -O-O-O-. They usually appear in the form of foul-smelling oily liquids. Their main use is in determining the structure of chemical compounds. As intermediates of ozonolysis, they are formed by an addition reaction of ozone and unsaturated compounds, and rapidly decompose to carbonyl compounds - aldehydes, ketones, peroxides.

See also

ar:أوزونيد de:Ozonid nds:Ozonid fi:Otsonidi