The structure of molecules or molecular ions that escapes description in terms of
conventional rules of valency and stereochemistry. Nonclassical structures are characteristic
of carbonium ions with hypercoordinated (see
hypercoordination) carbon atoms, e.g., methanium ion
1, pyramidal dication
C6H62+2 (
isomeric to benzene dication), and the molecular species whose structure cannot be adequately
represented by the equilibrium (2-norbornyl
cation,
3) or
resonance of two or more classical structures. From the stereochemical point of view, those
structures are assigned to the nonclassical type for which all tetracoordinate carbon
bonds extend into a single hemisphere, i.e., the
valenceangle of a carbon atom is greater than 180°. A hypothetical example is pyramidane,
4, the structure of which corresponds to a local minimum on the
C5H4
potential energy surface.
Source:
InChI=1/C5H4/c1-2-4-3(1)5(1,2)4/h1-4H
ICZKBCPBVASHJN-UHFFFAOYAZ
Cite as:
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.