Chemistry:Xenon fluoride nitrate

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Xenon fluoride nitrate
Xenon fluoride nitrate.svg
Identifiers
3D model (JSmol)
Properties
FNO3Xe
Molar mass 212.295 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Tracking categories (test):

Xenon fluoride nitrate, also known as fluoroxenonium nitrate, is the chemical compound with formula FXeONO2.[1][2]

Synthesis

This compound is formed via the reaction:[3]

[FXeOXeFXeF][AsF6] + 2NO2F → FXeONO2 + NO2AsF6.

Purification of FXeONO2 can then take place by dissolving in SO2ClF, which leaves the nitronium arsenic hexafluoride behind as a solid.[3]

An alternate low yield method to make FXeONO2 is to dissolve xenon difluoride in liquid dinitrogen tetroxide at 0 °C.[3]

XeF2 + NO+ + NO3 → FXeONO2 + NOF

This method is inefficient as not much nitrate ion exists in the liquid and the xenon fluoride nitrate decomposes.[3]

Another method claimed to make this substance is:[3]

XeF2 + HNO3 → FXeONO2 + HF

Properties

FXeONO2 is a white crystalline material.[3] The space group of the crystals is P21/c, which is monoclinic. The unit cell contains four molecules with a total volume of 386.6 Å3. The unit cell dimensions are a = 4.6663 Å, b = 8.799 Å c = 9.415 Å, with non-perpendicular angle β = 90.325°.[3] With a molecular weight of 212.3, the crystal has density 3.648. (These measurements at -173 °C.)[3] The bond lengths in the molecule are 1.992 Å for Xe–F, 2.126 Å for Xe–O, 1.36 Å for O–NO2, 1.199 for N–Ocis and 1.224 Å for N–Otrans.[3] The bond angles are 177.6° for F–Xe–O, 114.7° for Xe-O-N, 114.5° for (Xe)O–N–Ocis, 118.4° for (Xe)O–N–Otrans and 127.1° for Ocis–N–Otrans.[3] The bond lengths and angles on the xenon atom are similar to that in FXeOSO2F and FXeOTeF5, indicating a polar oxygen bond. The Xe–O–N angle is larger than those in halogen nitrates, which indicates a lower bond density for the Xe–O bond. The N–Ocis bond length is longer than the N–Otrans bond length, opposite to other halogen nitrates.[3]

FXeONO2 is not particularly stable and slowly breaks down at -78 °C, yielding XeF2·N2O4. This happens on a timescale of several days.[3] At 0 °C, FXeONO2 has a half life of seven hours, decomposing to XeF2.[3]

References

  1. Moran, Matthew D.; David S. Brock; Hélène P. A. Mercier; Gary J. Schrobilgen (2010). "Xe3OF3+, a Precursor to a Noble-Gas Nitrate; Syntheses and Structural Characterizations of FXeONO2, XeF2·HNO3, and XeF2·N2O4". Journal of the American Chemical Society 132 (39): 13823–13839. doi:10.1021/ja105618w. ISSN 0002-7863. PMID 20843046. 
  2. Atta-ur-Rahman (2006-01-01). Advances in Organic Synthesis: Modern Organofluorine Chemistry-Synthetic Aspects. Bentham Science Publishers. p. 78. ISBN 9781608051984. https://books.google.com/books?id=vkcLOFEo9xIC&pg=PA78. Retrieved 5 October 2014. 
  3. 3.00 3.01 3.02 3.03 3.04 3.05 3.06 3.07 3.08 3.09 3.10 3.11 3.12 Moran, Matthew D. (2007). Synthesis and Structural Characterization of new Xenon(II) Compounds and the Use of a Xenon(II) Cation as an Oxidant for the Preparation of Halogenated Hydrocarbons. McMaster University. pp. 42, 99–145. https://macsphere.mcmaster.ca/bitstream/11375/14167/1/fulltext.pdf. Retrieved 4 Oct 2014. 
Salts and covalent derivatives of the nitrate ion