Peroxycarbonate

Source: Wikipedia, the free encyclopedia.
α-Peroxycarbonate
Names
Preferred IUPAC name
Oxidocarbonate
Systematic IUPAC name
Oxocarbonate
Other names
Peroxycarbonate (Peroxocarbonate)
Percarbonate
Peroxidocarboxylate
Peroxidoformate
Dioxidan-2-idecarboxylate
Identifiers
3D model (
JSmol
)
ChemSpider
  • InChI=1S/CH2O4/c2-1(3)5-4/h4H,(H,2,3)/p-2
    Key: MMCOUVMKNAHQOY-UHFFFAOYSA-L
  • C(=O)([O-])O[O-]
Properties
CO42−
Molar mass 76.01 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

In

anion with formula CO2−
4
. It is an oxocarbon anion that consists solely of carbon and oxygen. It would be the anion of a hypothetical peroxycarbonic acid HO–CO–O–OH (sometimes peroxocarbonic acid).[1][2]
or the real hydroperoxyformic acid, HO-O-CO-OH (a.k.a. percarbonic acid, carbonoperoxoic acid, hydroxycarbonic acid).

The peroxycarbonate anion is formed, together with peroxydicarbonate C
2
O2−
6
, at the negative electrode during electrolysis of molten lithium carbonate.[3] Lithium peroxycarbonate can be produced also by combining carbon dioxide CO2 with lithium hydroxide in concentrated hydrogen peroxide H2O2 at −10 °C.[4]

Electrolysis of a solution of lithium carbonate at -30° to -40 °C yields a solution of the Lithium percarbonate, which can liberate iodine from potassium iodide instantaneously. The crystalline salt has not been isolated.

The peroxycarbonate anion has been proposed as an intermediate to explain the catalytic effect of CO2 on the oxidation of organic compounds by O2.[5]

The potassium and rubidium salts of the monovalent hydrogenperoxycarbonate anion (aka. hydroxycarbonate, biperoxycarbonate) H–O–O–CO
2
have also been obtained.[6][7][8][9]

See also

References

  1. .
  2. .
  3. .
  4. .
  5. ^ Mimoza Gjikaj (2001), "Darstellung und strukturelle Charakterisierung neuer Alkali- bzw. Erdalkalimetallperoxide, -hydrogenperoxide, -peroxocarbonate und -peroxohydrate" Archived 2012-02-25 at the Wayback Machine. Doctoral Thesis, University of Köln. 115 pages.
  6. PMID 29710903
    .
  7. ^ M. Mehta and A. Adam (1998), Z. Kristallogr., Suppl. Issue 15 p. 53. Cited by Gjikaj.
  8. ^ M. Mehta and A. Adam (1998), Z. Kristallogr., Suppl. Issue 15 p. 46. Cited by Gjikaj.