Comparison of Omega and PPP techniques for reactivity calculations in methyl-substituted naphthalenes
Author:
Publisher
Springer Science and Business Media LLC
Subject
Chiropractics,Physical and Theoretical Chemistry
Link
http://link.springer.com/content/pdf/10.1007/BF00527086.pdf
Reference13 articles.
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4. Longuet-Higgins, H. C., Salem, L.: Proc. Roy. Soc. (London) A 251, 172 (1959); - A 255, 435 (1960).
5. Ettinger, R.: Tetrahedron 20, 1579 (1964).
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1. Two-parameter ?-technique forMO calculations;International Journal of Quantum Chemistry;1977-05
2. Some analysis of the ?-Technique;Theoretica Chimica Acta;1974
3. Tight binding energy band structure calculations for phthalocyanines. I: β-hydrogen phthalocyanine;Journal of Physics C: Solid State Physics;1971-12-31
4. Electrophilic Substitution in Methyl-substituted Naphthalenes III. Correlation between Experimental Results and Molecular Orbital Calculations of Reactivity Indices;Canadian Journal of Chemistry;1971-12-15
5. Electrophilic Substitution in Methyl-Substituted Naphthalenes. II. The Hyperconjugative Model of the Methyl Group in PPP- and ω-Technique Calculations;Canadian Journal of Chemistry;1971-12-15
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