Oxygen difluoride
(Redirected from Difluorooxidane)
Oxygen difluoride | |
---|---|
IUPAC name | Oxygen difluoride |
Other names | Difluorine monoxide Difluorooxidane Difluoridooxygen |
Identifiers | |
InChI | InChI=1/F2O/c1-3-2 |
InChIKey | UJMWVICAENGCRF-UHFFFAOYAI |
Standard InChI | InChI=1S/F2O/c1-3-2 |
Standard InChIKey | UJMWVICAENGCRF-UHFFFAOYSA-N |
CAS number | [ | ]
EC number | |
ChemSpider | |
Properties[1][2][3] | |
Chemical formula | OF2 |
Molar mass | 55.996 g mol−1 |
Appearance | colourless gas |
Density | 1.90 g cm−3 (liquid, −223.8 °C) |
Melting point |
−223.8 °C (49.4 K) |
Boiling point |
−145.3 °C (127.9 K) |
Thermochemistry[4] | |
Std enthalpy of formation ΔfH |
+24.52 kJ mol−1 |
Standard molar entropy S |
247.46 J K−1 mol−1 |
Related compounds | |
Other fluorides of oxygen | Dioxygen difluoride |
Other compounds | Dichlorine monoxide Dibromine monoxide |
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
Oxygen difluoride, OF2, sometimes known as difluorine monoxide,[note 1] is the most stable of the binary compounds of oxygen and fluorine.[1][7] It was discovered as a byproduct of fluorine production using Moissan cells (electrolysis of HF/KF) due to small amounts of water in the electrolyte.[8] A more satisfactory method of preparation is the reaction of fluorine with 2% aqueous sodium hydroxide solution followed by fractional distillation of the gas produced.[9][10][11]
Structure
Oxygen difluoride has a bent C2v structure as expected by VSEPR theory. The oxygen–fluorine bond length is 140.5 pm and the bond angle at oxygen is 103°, consistent with single bonding and sp3 hybridization at oxygen.[1][7]
r(O–X)/pm | X–O–X/° | r(O–X)/pm | X–O–X/° | |||
---|---|---|---|---|---|---|
OF2 | 140.5 | 103 | F2O | 140.5 | 103 | |
HOF | 144.2 (O–F) 96.4 (O–H) |
97 | Cl2O | 170.0 | 110.9 | |
H2O | 95.7 | 104.5 | Br2O | 184.3 | 112.2 |
Notes and references
Notes
- ↑ Fluorine is more electronegative than oxygen, both on the normal numerical scales[5] and on the conventional series used in inorganic nomenclature,[6] so OF2 is usually considered a fluoride of oxygen and not an oxide of fluorine. However, other X2O compounds (X = Cl, Br) are considered to be halogen oxides, and so F2O is sometimes considered to be a member of this series, despite its somewhat different chemistry.[7]
References
- ↑ 1.0 1.1 1.2 Greenwood, Norman N.; Earnshaw, A. Chemistry of the Elements; Pergamon: Oxford, 1984; pp 748–49. ISBN 0-08-022057-6.
- ↑ CRC Handbook of Chemistry and Physics, 62nd ed.; Weast, Robert C., Ed.; CRC Press: Boca Raton, FL, 1981; p B-126. ISBN 0-8493-0462-8.
- ↑ Streng, Alex G. Miscibility and Compatibility of Some Liquid and Solidified Gases at Low Temperature. J. Chem. Eng. Data 1971, 16 (3), 357–59. DOI: 10.1021/je60050a024.
- ↑ Difluorine monoxide. In NIST Chemistry WebBook; National Institute for Standards and Technology, <http://webbook.nist.gov/cgi/inchi/InChI%3D1S/F2O/c1-3-2>. (accessed 31 December 2010).
- ↑ Allred, A. L. Electronegativity values from thermochemical data. J. Inorg. Nucl. Chem. 1961, 17 (3–4), 215–21. DOI: 10.1016/0022-1902(61)80142-5.
- ↑ Nomenclature of Inorganic Chemistry; IUPAC Recommendations 2005; Royal Society of Chemistry: Cambridge, 2005; p 260. ISBN 0-85404-438-8, <http://www.iupac.org/publications/books/rbook/Red_Book_2005.pdf>.
- ↑ 7.0 7.1 7.2 Cotton, F. Albert; Wilkinson, Geoffrey Advanced Inorganic Chemistry, 5th ed.; Wiley-Interscience: New York, 1988; pp 454–56. ISBN 0-471-84997-9.
- ↑ Lebeau, P.; Damiens, A. Sur l'existence d'un composé oxygéné du fluor. C. R. Hebd. Acad. Sci. Paris 1927, 185, 652–54, <http://gallica.bnf.fr/ark:/12148/bpt6k31384/f652.image>.
- ↑ Lebeau, P.; Damiens, A. Sur un nouveau mode de préparation du fluorure d'oxygène. C. R. Hebd. Acad. Sci. Paris 1929, 188, 1253–55, <http://gallica.bnf.fr/ark:/12148/bpt6k31417/f1253.image>.
- ↑ Yost, D. M. Oxygen Fluoride. Inorg. Synth. 1939, 1, 109–11.
- ↑ Appelman, Evan H.; Jache, Albert W. Concerning the mechanism of formation of oxygen difluoride. J. Am. Chem. Soc. 1987, 109 (6), 1754–57. DOI: 10.1021/ja00240a026.
External links
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