Misplaced Pages

Phosphorus pentafluoride

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.

This is an old revision of this page, as edited by Chem-awb (talk | contribs) at 01:01, 23 January 2009 ({{Chembox new --> {{Chembox, Replaced: {{Chembox new → {{chembox using AWB). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Revision as of 01:01, 23 January 2009 by Chem-awb (talk | contribs) ({{Chembox new --> {{Chembox, Replaced: {{Chembox new → {{chembox using AWB)(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff)
Phosphorus pentafluoride
Structure of the phosphorus pentafluoride molecule
Space-filling model of the phosphorus pentafluoride molecule
Names
IUPAC name Phosphorus pentafluoride
Other names Phosphorus(V) fluoride
Pentafluoridophosphorus
Pentafluorophosphorane
Identifiers
CAS Number
ECHA InfoCard 100.028.730 Edit this at Wikidata
CompTox Dashboard (EPA)
Properties
Chemical formula PF5
Molar mass 125.97 g/mol
Appearance colourless gas
Melting point −93.78 °C (179.4 K)
Boiling point −84.5 °C (188.7 K)
Solubility in water hydrolysis
Structure
Molecular shape trigonal bipyramidal
Dipole moment 0 D
Hazards
Flash point Non-flammable
Related compounds
Other anions Phosphorus pentachloride
Phosphorus pentabromide
Phosphorus pentaiodide
Other cations Arsenic pentafluoride
Antimony pentafluoride
Bismuth pentafluoride
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

Phosphorus pentafluoride, PF5, is a phosphorus halide. It's a colourless gas at room temperature and pressure.

Structure

Single-crystal X-ray studies indicate PF5 molecule has two distinct P−F bonds (axial and equatorial): P−Fax = 158.0 pm and P−Feq = 152.2 pm. Gas-phase electron diffraction analysis gives similar values: P−Fax = 158 pm and P−Feq = 153 pm.

F NMR spectroscopy, at temperatures as low as −100 °C fails to distinguish the axial from the equatorial fluorine environments. The apparent equivalency arises from the low barrier for pseudorotation via the Berry mechanism, by which the axial and equatorial fluorine atoms rapidly exchange positions. The apparent equivalency of the F centers in PF5 was first noted by Gutowsky.. The explanation was first described by R. Stephen Berry, after whom the Berry mechanism is named. Berry pseudorotation influences theF NMR spectrum of PF5 since NMR spectroscopy operates on a millisecond timescale. Electron diffraction and X-ray crystallography do not detect this effect as their timescales are significantly shorter than for NMR spectroscopy.

References

This article has an unclear citation style. The references used may be made clearer with a different or consistent style of citation and footnoting. (September 2007) (Learn how and when to remove this message)
  1. Gutowsky, H. S.; McCall, D. W.; Slichter, C. P. "Nuclear Magnetic Resonance Multiplets in Liquids" Journal of Chemical Physics 1953, volume 21, 279.

External links


Stub icon

This inorganic compound–related article is a stub. You can help Misplaced Pages by expanding it.

Categories: