Nitronium ion

The nitronium ion, [NO2]+, is a cation. It is an onium ion because its nitrogen atom has +1 charge, similar to ammonium ion [NH4]+. It is created by the removal of an electron from the paramagnetic nitrogen dioxide molecule NO2, or the protonation of nitric acid HNO3 (with removal of H2O).[2]

Not to be confused with Nitrosonium, a separate nitrogen-oxygen cation.
Nitronium ion
Skeletal formula of nitronium with some dimensions added
Skeletal formula of nitronium with some dimensions added
Spacefill model of nitronium
Spacefill model of nitronium
Ball and stick model of nitronium
Names
IUPAC name
Nitronium ion
Systematic IUPAC name
Dioxidonitrogen(1+)[1]
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
  • InChI=1S/NO2/c2-1-3/q+1
    Key: OMBRFUXPXNIUCZ-UHFFFAOYSA-N
  • O=[N+]=O
Properties
[NO2]+
Molar mass 46.005 g·mol−1
Thermochemistry
233.86 J K−1 mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

It is stable enough to exist in normal conditions, but it is generally reactive and used extensively as an electrophile in the nitration of other substances. The ion is generated in situ for this purpose by mixing concentrated sulfuric acid and concentrated nitric acid according to the equilibrium:

H2SO4 + HNO3 → HSO−4 + [NO2]+ + H2O

Structure

The nitronium ion is isoelectronic with carbon dioxide and nitrous oxide, and has the same linear structure and bond angle of 180°. For this reason it has a similar vibrational spectrum to carbon dioxide. Historically, the nitronium ion was detected by Raman spectroscopy, because its symmetric stretch is Raman-active but infrared-inactive. The Raman-active symmetrical stretch was first used to identify the ion in nitrating mixtures.[3]

Salts

A few stable nitronium salts with anions of weak nucleophilicity can be isolated. These include nitronium perchlorate [NO2]+[ClO4]−, nitronium tetrafluoroborate [NO2]+[BF4]−, nitronium hexafluorophosphate [NO2]+[PF6]−, nitronium hexafluoroarsenate [NO2]+[AsF6]−, and nitronium hexafluoroantimonate [NO2]+[SbF6]−. These are all very hygroscopic compounds.[4]

The solid form of dinitrogen pentoxide, N2O5, actually consists of nitronium and nitrate ions, so it is an ionic compound, nitronium nitrate [NO2]+[NO3]−, not a molecular solid. However, dinitrogen pentoxide in liquid or gaseous state is molecular and does not contain nitronium ions.[2][5]

The compounds nitryl fluoride, NO2F, and nitryl chloride, NO2Cl, are not nitronium salts but molecular compounds, as shown by their low boiling points (−72 °C and −6 °C respectively) and short nitrogen–halogen bond lengths (N–F 135 pm, N–Cl 184 pm).[6]

Addition of one electron forms the neutral nitryl radical, NO2•; in fact, this is fairly stable and known as the compound nitrogen dioxide.

The related negatively charged species is NO−2, the nitrite ion.

See also

References
  1. "dioxidonitrogen(1+) (CHEBI:29424)". Chemical Entities of Biological Interest (ChEBI). UK: European Bioinformatics Institute.
  2. Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
  3. Ingold, C. K.; Millen, D. J.; Poole, H. G. (1946). "Spectroscopic Identification of the Nitronium Ion". Nature. 158 (4014): 480–481. Bibcode:1946Natur.158..480I. doi:10.1038/158480c0. S2CID 4106964.
  4. Kenneth Schofield (1980). Aromatic nitration. CUP Archive. p. 88. ISBN 0-521-23362-3.
  5. Cantrell, C. A.; Davidson, J. A.; McDaniel, A. H.; Shetter, R. E.; Calvert, J. G. (1988). "The equilibrium constant for N2O5⇄NO2+NO3: Absolute determination by direct measurement from 243 to 397 K". The Journal of Chemical Physics. 88 (8): 4997–5006. doi:10.1063/1.454679.
  6. F. A. Cotton and G.Wilkinson, Advanced Inorganic Chemistry, 5th edition (1988), Wiley, p.333
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