Separation of the energetic and geometric contributions to aromaticity. Part VII. Changes of the aromatic character of the rings in naphthalene induced by the charged substituent CH2+. The dependence on the position of the substitution, torsion angle and the exocyclic bond length variation-Reference-Cited by-同舟云学术

Separation of the energetic and geometric contributions to aromaticity. Part VII. Changes of the aromatic character of the rings in naphthalene induced by the charged substituent CH2+. The dependence on the position of the substitution, torsion angle and the exocyclic bond length variation

Published:1998-03 Issue:13 Volume:54 Page:3303-3310
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Krygowski Tadeusz M.,Cyrański Michal K.,Nakata Kazuhide,Fujio Mizue,Tsuno Yuho

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference14 articles.

1. Ab initio MO study of benzylic cations?2. Steric effects on the resonance interaction and on the resonance demand in the Yukawa-Tsuno equation

2. Varying resonance demand in carbocationic systems

3. Changes of the Aromatic Character of the Ring in Exocyclically Substituted Derivatives of Benzylic Cation as a Result of Varying Charge at theexo-Carbon Atom

4. Separation of the energetic and geometric contributions to aromaticity. Part VI. Changes of the aromatic character of the rings in naphthalene, anthracene, phenanthrene and pyrene derivatives induced by the charged substituent CH2+

5. Definition of aromaticity basing on the harmonic oscillator model

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