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
Author:
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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2. Substituents and Environment Influences on Aromaticity of peri- and para-Substituted Naphthalenes;The Journal of Physical Chemistry A;2014-08-11
3. Aromatic character of heptafulvene and its complexes with halogen atoms;Journal of Molecular Modeling;2011-10-19
4. The role of substituent on the aromaticity variation of mono- and di-substituted aza analogs of indole;Journal of Molecular Structure: THEOCHEM;2010-07
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