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PF6.png
Hexafluorophosphate-anion-3D-vdW.png

Hexafluorophosphate is an anion with chemical formula of PF6. As a non-coordinating anion,[1][2][3] it is a poor nucleophile. It is prone to decomposition with the release of HF.[4]

Halide anions are easily replaced with PF6 by reaction with silver hexafluorophosphate. The precipitation of insoluble silver halide helps drive this reaction to completion. Some room temperature ionic liquids, such as bmimPF6, use PF6 as a counterion.[5]

Also, many imidazolium and formamidinium hexafluorophosphate salts are insoluble in water. The addition of ammonium hexafluorophosphate (NH4PF6) to an aqueous solution of the formamdinium/imidazolium salt results in a precipitate of the formamidinium/imidazolium hexafluorophosphate salt which can be gathered by filtration. This method can have advantages over the silver hexafluorophosphate method mentioned above in terms of expense and in systems where contamination with metal ions is strongly discouraged.

[edit] See also

[edit] References

  1. ^ In Sung Chun; Sung Jin Moon; Young Mee Na; Young-A. Lee; Kyung Ho Yoo; Ok-Sang Jung (September 2007). "Selective and sensitive recognition of hexafluorophosphate via an unusual equilibrium between a cationic square host and a PF6 guest". Inorganic Chemistry Communications 10 (9): 967–970. doi:10.1016/j.inoche.2007.05.008.  edit
  2. ^ Julian A. Davies (1996). Synthetic coordination chemistry: principles and practice. World Scientific. p. 165. ISBN 9810220847. 
  3. ^ Samuel Constant; Jerome Lacour (2005). Jean-Pierre Majoral. ed. New trends in hexacoordinated phosphorus chemistry. New aspects in phosphorus chemistry. 5. Springer. p. 3. ISBN 354022498X. 
  4. ^ Paul J. Dyson (2005). Tilmann J. Geldbach. ed. Metal catalysed reactions in ionic liquids. Catalysis by metal complexes. 29. Springer Science & Business. p. 27. ISBN 140203914X. 
  5. ^ Gordon, C. M.; John D. Holbrey; Alan R. Kennedy; Kenneth R. Seddon (1998). "Ionic liquid crystals: hexafluorophosphate salts". Journal of Materials Chemistry 8: 2627–2636. doi:10.1039/a806169f.  edit



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