Solid N2O5 is a salt, consisting of separated anions and cations. The cation is the linear nitronium ion NO2+ and the anion is the planar nitrate ion NO3−. Thus, the solid could be called nitronium nitrate. Both nitrogen centers have oxidation state +5.
The intact molecule O2N–O–NO2 exists in the gas phase (obtained by subliming N2O5) and when the solid is extracted into nonpolar solvents such as CCl4. In the gas phase, the O–N–O angle is 133° and the N–O–N angle is 114°. When gaseous N2O5 is cooled rapidly ("quenched"), one can obtain the metastable molecular form, which exothermically converts to the ionic form above −70 °C.
Reactions and applications
Dinitrogen pentoxide, for example as a solution in chloroform, has been used as a reagent to introduce the NO2 functionality. This nitration reaction is represented as follows:
For this use, dinitrogen pentoxide has been largely replaced by nitronium tetrafluoroborate [NO 2]+[BF 4]−. This salt retains the high reactivity of NO2+, but it is thermally stable, decomposing at about 180 °C (into NO2F and BF3). The reactivity of the NO2+ can be further enhanced with strong acids that generate the "super-electrophile" HNO22+.
Dinitrogen pentoxide is relevant to the preparation of explosives.
In the atmosphere, dinitrogen pentoxide is an important reservoir of the NOx species that are responsible for ozone depletion: its formation provides a null cycle with which NO and NO2 are temporarily held in an unreactive state.Mixing ratios of several ppbv have been observed in polluted regions of the night-time troposphere. Dinitrogen pentoxide has also been observed in the stratosphere at similar levels, the reservoir formation having been postulated in considering the puzzling observations of a sudden drop in stratospheric NO2 levels above 50 °N, the so-called 'Noxon cliff'.
Variations in N2O5 reactivity in aerosols can result in significant losses in tropospheric ozone, hydroxyl radicals, and NOx concentrations. Two important reactions of N2O5 in atmospheric aerosols are: 1) Hydrolysis to form nitric acid and 2) Reaction with halide ions, particularly Cl−, to form ClNO2 molecules which may serve as precursors to reactive chlorine atoms in the atmosphere.
N2O5 is a strong oxidizer that forms explosive mixtures with organic compounds and ammonium salts. The decomposition of dinitrogen pentoxide produces the highly toxic nitrogen dioxide gas.
^ abHolleman, Arnold Frederik; Wiberg, Egon (2001), Wiberg, Nils (ed.), Inorganic Chemistry, translated by Eagleson, Mary; Brewer, William, San Diego/Berlin: Academic Press/De Gruyter, ISBN0-12-352651-5
^Talawar, M. B.; et al. (2005). "Establishment of Process Technology for the Manufacture of Dinitrogen Pentoxide and its Utility for the Synthesis of Most Powerful Explosive of Today—CL-20". Journal of Hazardous Materials. 124 (1–3): 153–64. doi:10.1016/j.jhazmat.2005.04.021. PMID15979786.
^Finlayson-Pitts, Barbara J.; Pitts, James N. (2000). Chemistry of the upper and lower atmosphere : theory, experiments, and applications. San Diego: Academic Press. ISBN9780080529073. OCLC162128929.
^HaiChao Wang; et al. (2017). "High N2O5 Concentrations Observed in Urban Beijing: Implications of a Large Nitrate Formation Pathway". Environmental Science and Technology Letters. 4 (10): 416–420. doi:10.1021/acs.estlett.7b00341.
^Macintyre, H. L.; Evans, M. J. (2010-08-09). "Sensitivity of a global model to the uptake of N2O5 by tropospheric aerosol". Atmospheric Chemistry and Physics. 10 (15): 7409–7414. doi:10.5194/acp-10-7409-2010. ISSN1680-7324.
^Brown, S. S.; Dibb, J. E.; Stark, H.; Aldener, M.; Vozella, M.; Whitlow, S.; Williams, E. J.; Lerner, B. M.; Jakoubek, R. (2004-04-16). "Nighttime removal of NOx in the summer marine boundary layer". Geophysical Research Letters. 31 (7): n/a. doi:10.1029/2004GL019412. ISSN1944-8007.
^Kelleher, Patrick J.; Menges, Fabian S.; DePalma, Joseph W.; Denton, Joanna K.; Johnson, Mark A.; Weddle, Gary H.; Hirshberg, Barak; Gerber, R. Benny (2017-09-18). "Trapping and Structural Characterization of the XNO2·NO3– (X = Cl, Br, I) Exit Channel Complexes in the Water-Mediated X– + N2O5 Reactions with Cryogenic Vibrational Spectroscopy". The Journal of Physical Chemistry Letters. 8 (19): 4710–4715. doi:10.1021/acs.jpclett.7b02120. ISSN1948-7185. PMID28898581.