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Carbon trioxide

From Wikipedia, the free encyclopedia
For polyatomic ion CO2−
3
, seeCarbonate. For the UK postal district, seeCO postcode area.
Carbon trioxide
The Cs, D3h, and C2v isomers of carbon trioxide
Names
IUPAC names
Carbon trioxide
C2v isomer:
  • Dioxiran-3-one

D3h isomer:

  • Carbonate radical
Systematic IUPAC name
C2v isomer:
  • Peroxycarbonic anhydride

D3h isomer:

  • Trioxidocarbon(2•)
Other names
Cs isomer:
  • Oxidooxymethanone
  • Peroxycarbonite radical
Identifiers
3D model (JSmol)
  • InChI=1S/CO3/c2-1-3-4-1
    Key: NPDDCAZCWJWIBW-UHFFFAOYSA-N
  • Cs: O=[C]O[O]
  • D3h: O=C([O])[O]
  • C2v: O=C1OO1
Properties
CO3
Molar mass60.008 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Carbon trioxide (CO3) is an unstableoxide ofcarbon (anoxocarbon). The possibleisomers of carbon trioxide include ones withmolecular symmetry point groupsCs,D3h, andC2v. TheC2v state, consisting of adioxirane, has been shown to be theground state of the molecule.[1] Carbon trioxide should not be confused with the stablecarbonate ion (CO2−
3
).

Carbon trioxide can be produced, for example, in the drift zone of a negativecorona discharge by reactions betweencarbon dioxide (CO2) and theatomic oxygen (O) created from molecular oxygen by free electrons in theplasma.[2] Another reported method isphotolysis of ozone O3 dissolved in liquid CO2, or in CO2/SF6 mixtures at −45 °C (228 K; −49 °F), irradiated with light of 253.7 nm. The formation of CO3 is inferred but it appears to decay spontaneously by the route

2 CO3 → 2 CO2 + O2

with a lifetime much shorter than 1 minute.[3] Carbon trioxide can be made by blowingozone atdry ice (solid CO2), and it has also been detected in reactions betweencarbon monoxide (CO) andmolecular oxygen (O2). Along with the ground state C2visomer,[4] the firstspectroscopic detection of the D3h isomer was in electron-irradiated ices ofcarbon dioxide.[5]

References

[edit]
  1. ^T. Kowalczyk; A. I. Krylov (Aug 2007). "Electronic structure of carbon trioxide and vibronic interactions involving Jahn–Teller states".J. Phys. Chem. A.111 (33):8271–8276.Bibcode:2007JPCA..111.8271K.doi:10.1021/jp073627d.ISSN 1089-5639.PMID 17661455.
  2. ^Sabin, J. R; Kim, H (1971). "A theoretical study of the structure and properties of carbon trioxide".Chemical Physics Letters.11 (5):593–597.Bibcode:1971CPL....11..593S.doi:10.1016/0009-2614(71)87010-0.
  3. ^DeMore W. B.; Jacobsen C. W. (1969). "Formation of carbon trioxide in the photolysis of ozone in liquid carbon dioxide".Journal of Physical Chemistry.73 (9):2935–2938.doi:10.1021/j100843a026.
  4. ^Bennett, Chris J.; Jamieson, C.; Mebel, Alexander M.; Kaiser, Ralf I. (2004). "Untangling the formation of the cyclic carbon trioxide isomer in low temperature carbon dioxide ices".Physical Chemistry Chemical Physics.6 (4): 735.Bibcode:2004PCCP....6..735B.doi:10.1039/b315626p.S2CID 51769127.
  5. ^Jamieson, Corey S.; Mebel, Alexander M.; Kaiser, Ralf I. (2006). "Identification of the D3h Isomer of Carbon Trioxide (CO3) and Its Implications for Atmospheric Chemistry".ChemPhysChem.7 (12):2508–2513.doi:10.1002/cphc.200600390.PMID 17029325.

Further reading

[edit]
Common oxides
Exotic oxides
Polymers
Compounds derived from oxides
Mixed oxidation states
+1 oxidation state
+2 oxidation state
+3 oxidation state
+4 oxidation state
+5 oxidation state
+6 oxidation state
+7 oxidation state
+8 oxidation state
Related
Oxides are sorted byoxidation state.Category:Oxides
Compounds
Carbon ions
Nanostructures
Oxides and related
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