A molozonide (or "molecular ozonide") is a 1,2,3-trioxolane, which can also be thought of a cyclic dialkyl

trioxidane Trioxidane (systematically named μ-trioxidanediidodihydrogen), also called dihydrogen trioxide, is an inorganic compound with the chemical formula (can be written as or ). It is one of the unstable hydrogen polyoxides. In aqueous solutions, ...

. Molozonides are formed by

cycloaddition In organic chemistry, a cycloaddition is a chemical reaction in which "two or more Unsaturated hydrocarbon, unsaturated molecules (or parts of the same molecule) combine with the formation of a cyclic adduct in which there is a net reduction of th ...

ozone Ozone (), or trioxygen, is an inorganic molecule with the chemical formula . It is a pale blue gas with a distinctively pungent smell. It is an allotrope of oxygen that is much less stable than the diatomic allotrope , breaking down in the lo ...

and an

alkene In organic chemistry, an alkene is a hydrocarbon containing a carbon–carbon double bond. Alkene is often used as synonym of olefin, that is, any hydrocarbon containing one or more double bonds.H. Stephen Stoker (2015): General, Organic, an ...

during

ozonolysis In organic chemistry, ozonolysis is an organic reaction where the unsaturated bonds of alkenes (), alkynes (), or azo compounds () are cleaved with ozone (). Alkenes and alkynes form organic compounds in which the multiple carbon–carbon bond ...

, as a transient intermediate which quickly rearranges to give the

ozonide Ozonide is the polyatomic anion . Cyclic organic compounds formed by the addition of ozone () to an alkene are also called ozonides. Ionic ozonides Inorganic ozonides are dark red salts. The anion has the bent shape of the ozone molecule. Inor ...

(1,2,4-trioxolane), the relatively stable product generated immediately prior to reductive or oxidative cleavage to form alcohols, carbonyl compounds, or derivatives thereof.

References

Oxygen heterocycles Polyoxides Heterocyclic compounds with 1 ring {{Heterocyclic-stub