Aromaticity of Non-Alternant Annulenoannulenes and of Corannulenes

Israel Agranat; B. Andes Hess; L. J. Schaad

doi:10.1351/pac198052061399

Aromaticity of Non-Alternant Annulenoannulenes and of Corannulenes

Israel Agranat, B. Andes Hess, L. J. Schaad

Institute of Chemistry

Research output: Contribution to journal › Article › peer-review

85 Scopus citations

Abstract

Resonance energies of non-alternant annulenoannulenes and corannulenes have been calculated. The aromatic character of the former appears to be dominated by their periphery, in contrast to the behavior of the alternant annulenoannulenes. For the corannulenes no simple systematic behavior is apparent. Kekulene and many compounds of similar structure are predicted to be aromatic regardless of their inner and outer peripheral circuits.

Original language	English
Pages (from-to)	1399-1407
Number of pages	9
Journal	Pure and Applied Chemistry
Volume	52
Issue number	6
DOIs	https://doi.org/10.1351/pac198052061399
State	Published - 1980

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abstract = "Resonance energies of non-alternant annulenoannulenes and corannulenes have been calculated. The aromatic character of the former appears to be dominated by their periphery, in contrast to the behavior of the alternant annulenoannulenes. For the corannulenes no simple systematic behavior is apparent. Kekulene and many compounds of similar structure are predicted to be aromatic regardless of their inner and outer peripheral circuits.",

author = "Israel Agranat and Hess, {B. Andes} and Schaad, {L. J.}",

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N2 - Resonance energies of non-alternant annulenoannulenes and corannulenes have been calculated. The aromatic character of the former appears to be dominated by their periphery, in contrast to the behavior of the alternant annulenoannulenes. For the corannulenes no simple systematic behavior is apparent. Kekulene and many compounds of similar structure are predicted to be aromatic regardless of their inner and outer peripheral circuits.

AB - Resonance energies of non-alternant annulenoannulenes and corannulenes have been calculated. The aromatic character of the former appears to be dominated by their periphery, in contrast to the behavior of the alternant annulenoannulenes. For the corannulenes no simple systematic behavior is apparent. Kekulene and many compounds of similar structure are predicted to be aromatic regardless of their inner and outer peripheral circuits.

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Aromaticity of Non-Alternant Annulenoannulenes and of Corannulenes

Abstract

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