In chemistry, molecular autoionization (or self-ionization) is a chemical 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]: 163  In most cases the oxidation number on all atoms in such a reaction remains unchanged. Such autoionization can be protic (H+
 transfer), or non-protic.

Examples

Protic solvents

Protic solvents often undergo some autoionization (in this case autoprotolysis):

  • [1]: 217 
  • [1]: 223 
    • Here proton transfer between two HF combines with homoassociation of F− and a third HF to form HF−2[1]: 221 


Structure of solid phosphorus pentachloride, illustrating its autoionization into PCl+4 and PCl−6.[2]

Non-protic solvents

  • [1]: 224 

These solvents all possess atoms with odd atomic numbers, either nitrogen or a halogen. Such atoms enable the formation of singly charged, nonradical ions (which must have at least one odd atomic number atom), which are the most favorable autoionization products. Protic solvents, mentioned previously, use hydrogen for this role. Autoionization would be much less favorable in solvents such as sulfur dioxide or carbon dioxide, which have only even atomic number atoms.

Coordination chemistry

Autoionization is not restricted to neat liquids or solids. Solutions of metal complexes exhibit this property. For example, compounds of the type FeX2(terpyridine) (where X = Cl or Br) are unstable with respect to autoionization forming [Fe(terpyridine)2]2+[FeX4]2−.[3]

See also

References

  1. 1 2 3 4 5 6 Housecroft C.E.; Sharpe A.G. (2005). Inorganic Chemistry (2nd ed.). Pearson. ISBN 0130-39913-2.
  2. ↑ Finch, A.; Fitch, A.N.; Gates, P.N. (1993). "Crystal and Molecular structure of a metastable modification of phosphorus pentachloride". Journal of the Chemical Society, Chemical Communications (11): 957–958. doi:10.1039/C39930000957.
  3. ↑ Kamata, K.; Suzuki, A.; Nakai, Y.; Nakazawa, H., "Catalytic Hydrosilylation of Alkenes by Iron Complexes Containing Terpyridine Derivatives as Ancillary Ligands", Organometallics 2012, 31, 3825-3828. doi:10.1021/om300279t


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