Hyperconjugative π-Aromaticity:  How To Make Cyclopentadiene Aromatic

Author:

Nyulászi László1,Schleyer Paul von Ragué1

Affiliation:

1. Contribution from the Fachbereich Chemie, Universität Kaiserslautern, Erwin-Schrödinger-Strasse 54, D-67663 Kaiserslautern, Rhineland-Palatinate, Germany, Institut für Organische Chemie, Computer Chemistry Center, Universität Erlangen-Nürnberg, Henkestrasse 42, D-91054 Erlangen, Germany, and Computational Chemistry Annex, University of Georgia, Athens, Georgia 30602-2525

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Reference23 articles.

1. Mulliken R. S.; Rieke, C. A.; Brown, W. G.J. Am. Chem. Soc.1941,63, 41. Dauben, H. J., Jr.; Wilson, J. D.; Laity, J. L.J. Am. Chem. Soc.1968,91, 811. Dauben, H. J., Jr.; Wilson, J. D.; Laity, J. L.J. Am. Chem. Soc.1968,91, 1911. Dauben, H. J., Jr.; Wilson, J. D.; Laity, J. L. InNonbenzoidAromatics; Synder, J. P., Ed.; Academic Press:  New York, 1971; Vol. II, pp 167−206. Labarre, J.F.; Crasnier, F.Top. Curr. Chem.1971,24, 33. Haddon, R. C.; Haddon, V. R.; Jackman, L. M.Top. Curr. Chem.1971,16, 112.

2. Molecular Zeeman effect of cyclopentadiene and isoprene and comparison of the magnetic susceptibility anisotropies

3. Aromaticity of five-membered heterocycles: an experimentally convenient theoretical model for prediction of relative aromaticity

4. Aromatizität und Antiaromatizität in fünfgliedrigen C4H4X-Ringsystemen: beschreibbar durch „klassische” und „magnetische” Konzepte

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