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delocalization

in theoretical organic chemistry
Redistribution of the valence-shell electron density throughout a molecular entity as compared with some localized models (individual atoms in their valence states, separated bonds or fragments). Different topological modes of the electron delocalization include:
  1. ribbon delocalization of either π- or σ-electrons (i.e., electrons occupying respectively π- and σ-orbitals)
  2. surface delocalization of σ-electrons occurring through an overlap of radially oriented σ-orbitals of a cyclic molecule, as is the case of cyclopropane; and
  3. volume delocalization of σ-electrons through an overlap of σ-orbitals directed inside a molecular polyhedron, as is the case in tetrahedrane.
Source:
PAC, 1999, 71, 1919 (Glossary of terms used in theoretical organic chemistry) on page 1933
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IUPAC. Compendium of Chemical Terminology, 2nd ed. (the "Gold Book"). Compiled by A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford (1997). XML on-line corrected version: http://goldbook.iupac.org (2006-) created by M. Nic, J. Jirat, B. Kosata; updates compiled by A. Jenkins. ISBN 0-9678550-9-8. https://doi.org/10.1351/goldbook.
Last update: 2014-02-24; version: 2.3.3.
DOI of this term: https://doi.org/10.1351/goldbook.DT07019.
Original PDF version: http://www.iupac.org/goldbook/DT07019.pdf. The PDF version is out of date and is provided for reference purposes only. For some entries, the PDF version may be unavailable.
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