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Xenon tetrafluoride

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Chemical compound
Xenon tetrafluoride
XeF 4 crystals. 1962.
XeF
4
crystals. 1962.
Names IUPAC name
Xenon tetrafluoride
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.033.858 Edit this at Wikidata UNII
  • InChI=1S/F4Xe/c1-5(2,3)4 checkY
    Key: RPSSQXXJRBEGEE-UHFFFAOYSA-N checkY
  • InChI=1/F4Xe/c1-5(2,3)4
    Key: RPSSQXXJRBEGEE-UHFFFAOYAW
  • F[Xe](F)(F)F
Properties XeF
4
Molar mass 207.2836 g mol−1 Appearance White solid Density 4.040 g cm−3, solid Melting point 117 °C (243 °F; 390 K) sublimes[1] Reacts Structure D4h square planar 0 D Thermochemistry 146 J·mol−1·K−1[2] −251 kJ·mol−1[2]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify  (what is checkYN ?)
Chemical compound

Xenon tetrafluoride is a chemical compound with chemical formula XeF
4
. It was the first discovered binary compound of a noble gas.[3] It is produced by the chemical reaction of xenon with fluorine:[4] [5]

Xe + 2 F
2
XeF
4

This reaction is exothermic, releasing an energy of 251 kJ/mol.[3]

Xenon tetrafluoride is a colorless crystalline solid that sublimes at 117 °C. Its structure was determined by both NMR spectroscopy and X-ray crystallography in 1963.[6] [7] The structure is square planar, as has been confirmed by neutron diffraction studies.[8] According to VSEPR theory, in addition to four fluoride ligands, the xenon center has two lone pairs of electrons. These lone pairs are mutually trans.

Synthesis

[edit ]

The original synthesis of xenon tetrafluoride occurred through direct 1:5-molar-ratio combination of the elements in a nickel (Monel) vessel at 400 °C.[9] The nickel does not catalyze the reaction,[citation needed ] but rather protects the container surfaces against fluoride corrosion. Controlling the process against impurities is difficult, as xenon difluoride (XeF
2
), tetrafluoride, and hexafluoride (XeF
6
) are all in chemical equilibrium, the difluoride favored at low temperatures and little fluorine and the hexafluoride favored at high temperatures and excess fluorine.[9] [10] Fractional sublimation (xenon tetrafluoride is particularly involatile) or other equilibria generally allow purification of the product mixture.[9]

The elements combine more selectively when γ- or UV-irradiated in a nickel container or dissolved in anhydrous hydrogen fluoride with catalytic oxygen. That reaction is believed selective because dioxygen difluoride at standard conditions is too weak an oxidant to generate xenon(VI) species.[9]

Alternatively, fluoroxenonium perfluorometallate salts pyrolyze to XeF4.[9]

Reactions

[edit ]

Xenon tetrafluoride hydrolyzes at low temperatures to form elemental xenon, oxygen, hydrofluoric acid, and aqueous xenon trioxide:[11]

  6 X e F 4 + 12 H 2 O 2 X e O 3 + 4 X e + 3 O 2 + 24 H F {\displaystyle {\rm {\ 6XeF_{4}+12H_{2}O\rightarrow 2XeO_{3}+4Xe\uparrow +3O_{2}\uparrow +24HF}}} {\displaystyle {\rm {\ 6XeF_{4}+12H_{2}O\rightarrow 2XeO_{3}+4Xe\uparrow +3O_{2}\uparrow +24HF}}}

It is used as a precursor for synthesis of all tetravalent Xe compounds.[9] Reaction with tetramethylammonium fluoride gives tetramethylammonium pentafluoroxenate, which contains the pentagonal XeF
5
anion. The XeF
5
anion is also formed by reaction with cesium fluoride:[12]

CsF + XeF
4
CsXeF
5

Reaction with bismuth pentafluoride (BiF
5
) forms the XeF+
3
cation:[13]

BiF
5
+ XeF
4
→ XeF3BiF6

The XeF+
3
cation in the salt XeF3Sb2F11 has been characterized by NMR spectroscopy.[14]

At 400 °C, XeF
4
reacts with xenon to form XeF
2
:[10]

XeF4 + Xe → 2 XeF2

The reaction of xenon tetrafluoride with platinum yields platinum tetrafluoride and xenon:[10]

XeF4 + Pt → PtF4 + Xe

Applications

[edit ]

Xenon tetrafluoride has few applications. It has been shown to degrade silicone rubber for analyzing trace metal impurities in the rubber. XeF
4
reacts with the silicone to form simple gaseous products, leaving a residue of metal impurities.[15]

References

[edit ]
  1. ^ Holleman, Arnold F.; Wiberg, Egon (2001). Wiberg, Nils (ed.). Inorganic Chemistry. Translated by Eagleson, Mary; Brewer, William. Academic Press. p. 394. ISBN 0-12-352651-5.
  2. ^ a b Zumdahl, Steven S. (2009). Chemical Principles (6th ed.). Houghton Mifflin Company. p. A23. ISBN 978-0-618-94690-7.
  3. ^ a b Zumdahl (2007). Chemistry. Boston: Houghton Mifflin. p. 243. ISBN 978-0-618-52844-8.
  4. ^ Claassen, H. H.; Selig, H.; Malm, J. G. (1962). "Xenon Tetrafluoride". J. Am. Chem. Soc. 84 (18): 3593. doi:10.1021/ja00877a042.
  5. ^ Chernick, C. L.; Claassen, H. H.; Fields, P. R.; Hyman, H. H.; Malm, J. G.; Manning, W. M.; Matheson, M. S.; Quarterman, L. A.; Schreiner, F.; Selig, H. H.; Sheft, I.; Siegel, S.; Sloth, E. N.; Stein, L.; Studier, M. H.; Weeks, J. L.; Zirin, M. H. (1962). "Fluorine Compounds of Xenon and Radon". Science. 138 (3537): 136–138. Bibcode:1962Sci...138..136C. doi:10.1126/science.138.3537.136. PMID 17818399. S2CID 10330125.
  6. ^ Brown, Thomas H.; Whipple, E. B.; Verdier, Peter H. (1963). "Xenon Tetrafluoride: Fluorine-19 High-Resolution Magnetic Resonance Spectrum". Science. 140 (3563): 178. Bibcode:1963Sci...140..178B. doi:10.1126/science.140.3563.178. PMID 17819836. S2CID 35981023.
  7. ^ Ibers, James A.; Hamilton, Walter C. (1963). "Xenon Tetrafluoride: Crystal Structure". Science. 139 (3550): 106–107. Bibcode:1963Sci...139..106I. doi:10.1126/science.139.3550.106. PMID 17798707. S2CID 42119788.
  8. ^ Burns, John H.; Agron, P. A.; Levy, Henri A (1963). "Xenon Tetrafluoride Molecule and Its Thermal Motion: A Neutron Diffraction Study". Science. 139 (3560): 1208–1209. Bibcode:1963Sci...139.1208B. doi:10.1126/science.139.3560.1208. PMID 17757912. S2CID 35858682.
  9. ^ a b c d e f Haner, Jamie; Schrobilgen, Gary J. (2015). "The Chemistry of Xenon(IV)". Chem. Rev. 115 (2): 1255–1295. doi:10.1021/cr500427p. ISSN 0009-2665. PMID 25559700.
  10. ^ a b c Bard, Allen J.; Parsons, Roger; Jordan, Joseph; International Union of Pure and Applied Chemistry (1985). Standard Potentials in Aqueous Solution. CRC Press. pp. 767–768. ISBN 0-8247-7291-1.
  11. ^ Williamson; Koch, C. W. (Mar 1963). "Xenon Tetrafluoride: Reaction with Aqueous Solutions". Science. 139 (3559): 1046–1047. Bibcode:1963Sci...139.1046W. doi:10.1126/science.139.3559.1046. ISSN 0036-8075. PMID 17812981. S2CID 33320384.
  12. ^ Harding, Charlie; Johnson, David Arthur; Janes, Rob (2002). Elements of the p Block. Molecular World. Vol. 9. Royal Society of Chemistry. p. 93. ISBN 0-85404-690-9.
  13. ^ Suzuki, Hitomi; Matano, Yoshihiro (2001). Organobismuth chemistry. Elsevier. p. 8. ISBN 0-444-20528-4.
  14. ^ Gillespie, R. J.; Landa, B.; Schrobilgen, G. J. (1971). "Trifluoroxenon(IV) μ-fluoro-bispentafluoroantimonate(V): the XeF+
    3
    cation". Journal of the Chemical Society D: Chemical Communications (23): 1543–1544. doi:10.1039/C29710001543.
  15. ^ Rigin, V.; Skvortsov, N. K.; Rigin, V. V. (March 1997). "Xenon tetrafluoride as a decomposition agent for silicone rubber for isolation and atomic emission spectrometric determination of trace metals". Analytica Chimica Acta. 340 (1–3): 1–3. Bibcode:1997AcAC..340....1R. doi:10.1016/S0003-2670(96)00563-6.
[edit ]
Helium compounds
Neon compounds
Argon compounds
Krypton compounds
Xenon compounds
Xe(0)
Xe(I)
Xe(II)
Xe(IV)
Xe(VI)
Xe(VIII)
Radon compounds
Rn(II)
Rn(IV)
Rn(VI)
Oganesson compounds
(predicted)
Og(0)
  • Og2
  • OgH+
Og(II)
  • OgF2
  • OgCl2
  • OgO
Og(IV)
  • OgF4
  • OgO2
  • OgTs4
Og(VI)
  • OgF6
Salts and covalent derivatives of the fluoride ion
HF ?HeF2
FrF RaF2   LrF3 Rf Db Sg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
PF6, AsF6, SbF6 compounds
AlF2−5, AlF3−6 compounds
chlorides, bromides, iodides
and pseudohalogenides
SiF2−6, GeF2−6 compounds
Oxyfluorides
Organofluorides
with transition metal,
lanthanide, actinide, ammonium
nitric acids
bifluorides
thionyl, phosphoryl,
and iodosyl

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