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Monocyclic planar (or almost planar) systems of trigonally (or sometimes digonally) hybridized atoms that contain (4n + 2) π-electrons (where n is a non-negative integer) will exhibit aromatic character. The rule is generally limited to n = 0–5. This rule is derived from the Hückel MO calculation on planar monocyclic conjugated hydrocarbons (CH)m where m is an integer equal to or greater than 3 according to which (4n + 2) π-electrons are contained in a closed-shell system. Examples of systems that obey the Hückel rule include:
H02867
Systems containing 4n π-electrons (such as cyclobutadiene and the cyclopentadienyl cation) are 'antiaromatic'.
Source:
PAC, 1994, 66, 1077 (Glossary of terms used in physical organic chemistry (IUPAC Recommendations 1994)) on page 1122
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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.
DOI of this term: https://doi.org/10.1351/goldbook.H02867
Original PDF version (may be out of date): http://www.iupac.org/goldbook/H02867.pdf.
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