Ozonide

Source: Wikipedia, the free encyclopedia.
Ozonide
Names
IUPAC name
Trioxidan-1-id-3-yl
Identifiers
3D model (
JSmol
)
ChEBI
ChemSpider
25183
  • InChI=1S/HO3/c1-3-2/h1H/p-1
    Key: WURFKUQACINBSI-UHFFFAOYSA-M
  • InChI=1/HO3/c1-3-2/h1H/p-1
    Key: WURFKUQACINBSI-REWHXWOFAH
  • [O-]O[O]
  • [O-][O+][O-]
Properties
O3
Molar mass 47.997 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Ozonide is the polyatomic anion O3. Cyclic organic compounds formed by the addition of ozone (O3) to an alkene are also called ozonides.

Ionic ozonides

Inorganic ozonides[1] are dark red salts. The anion has the bent shape of the ozone molecule.

Inorganic ozonides are formed by burning

NaOH and NaO2, was previously thought to be impossible to obtain in pure form.[2] However, with the help of cryptands and methylamine, pure sodium ozonide may be obtained as red crystals isostructural to NaNO2.[3]

Ionic ozonides are being investigated[

liquid ammonia
, is stable up to 348 K (75 °C):

[4]

Alkaline earth metal ozonide compounds have also become known. For instance, magnesium ozonide complexes have been isolated in a low-temperature argon matrix.[5]

Covalent singly bonded structures

Phosphite ozonides, (RO)3PO3, are used in the production of

phosphate ester:[6][7]

Molozonides

Formation of an organic ozonide. The second arrow represents several steps as shown in ozonolysis.

carbonyl compounds: aldehydes, ketones, peroxides
.

See also

References

  1. ^ Cotton, F. A.; Wilkinson, G. (1988). Advanced Inorganic Chemistry (5th ed.). p. 462.
  2. .
  3. .
  4. .
  5. ^ Wang, Guanjun & Gong, Yu & Zhang, Qingqing & Zhou, Mingfei. "Formation and Characterization of Magnesium Bisozonide and Carbonyl Complexes in Solid Argon". The journal of physical chemistry. A. 114 (2010). 10803-9. https://www.researchgate.net/publication/46392397_Formation_and_Characterization_of_Magnesium_Bisozonide_and_Carbonyl_Complexes_in_Solid_Argon
  6. .
  7. .
  8. .
  9. ^ Ozonolysis mechanism on Organic Chemistry Portal site

External links