Molecular autoionization

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Molecular autoionization (or self-ionization) is a reaction between molecules of the same substance to produce ions. If a pure liquid partially dissociates into ions, it is said to be self-ionizing.[1] The oxidation number on all atoms in such a reaction remains unchanged. Such autoionization can be protic (H+ transfer), or non-protic. Some examples of each are:

Protic solvents:

2 H2OH3O+ + OH. The self-ionization of water is particularly well studied, due to its implications for acid-base chemistry of aqueous solutions.

2 NH3NH4+ + NH2 [2]
2 H2SO4H3SO4+ + HSO4 [3]
3 HF ⇌ H2F+ + HF2 [4] Here proton transfer between two HF combines with homoassociation of F and a third HF to form HF2.

Non-protic solvents:

2 PF5 ⇌ PF6 + PF4+
2 N2O4 ⇌ NO+ + NO3 [2]
2 BrF3 ⇌ BrF2+ + BrF4 [5]

The self-ionization 2 SO2SO32− + SO2+ has also been proposed, but must be considered improbable because it would require the separation of doubly charged ions.[2]

Molecular autoionization can occur in gases or solids, but occurs most readily in liquids. In gases, the molecules are so far apart that ion formation is very unfavorable, and in solids, there is not enough molecular movement. As long as the phase remains constant, autoionization normally increases substantially with increasing pressure.

See also

References

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  1. Housecroft C.E. and Sharpe A.G. Inorganic Chemistry (2nd ed., Pearson 2005) p.163 ISBN 0130-39913-2
  2. 2.0 2.1 2.2 Housecroft and Sharpe p.217
  3. Housecroft and Sharpe p.223
  4. Housecroft and Sharpe p.221
  5. Housecroft and Sharpe p.224