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Aza[10]annulene: Next Higher Aromatic Analogue of Pyridine
Holger F. Bettinger1, Horst M. Sulzbach, Paul v. R. Schleyer
1Center for Computational Quantum Chemistry, The University of Georgia, Athens, Georgia 30602-2525.
The Journal of Organic Chemistry
|October 25, 2001
Abstract:
The aza[10]annulene isomers (CH)(9)N derived from "twist", "heart", "naphthalene-like", and "azulene-like" [10]annulenes by replacement of a CH group by nitrogen were investigated at the CCSD(T)/DZd//B3LYP/6-311+G level of theory. Except for the twist structure, all aza[10]annulenes studied were found to be aromatic. As the transannular repulsion is reduced in the aza[10]annulenes, the aromatic isomers become competitive energetically with the twist form.