A molecular orbital study comparing the effects of heteroatom substitution in trans-1,3-butadiene, all-trans-1,3,5-hexatriene, and benzene
Author:
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry,Condensed Matter Physics
Link
http://link.springer.com/content/pdf/10.1007/BF01374481.pdf
Reference32 articles.
1. Albert, A.Heterocyclic Chemistry: An Introduction, Essential Books, Fairlawn, NJ, 1959, p. 40.
2. George, P.; Bock, C. W.; Trachtman, M.J. Chem. Ed. 1984,61, 225. Empirical resonance energies, for example the values calculated using Pauling's or Kistiakowsky's procedures, are shown to be the enthalpy changes for reactions of the aromatic molecule and selected reference molecules. Since reaction enthalpies are phenomenological in nature and not related to any particular theory of aromaticity, the more general term ?stabilization energy? is used in this contribution.
3. George, P.; Trachtman, M.; Bock, C. W.; Brett, A. M.Theoret. Chim. Acta (Berlin) 1975,38, 121.
4. George, P.; Trachtman, M.; Bock, C. W.; Brett, A. M.J. Chem. Soc., Perkin Trans. 1976,2, 1222.
5. George, P.; Trachtman, M.; Brett, A. M.; Bock, C. W.J. Chem. Soc., Perkin Trans. 1977,2, 1036.
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