Aromaticity of peri- and para-Substituted Naphthalene-1-carbaldehyde. Comparison with 1-Nitronaphthalene
Author:
Affiliation:
1. Faculty of Pharmacy, Wroclaw Medical University, Borowska 211a, 50-556 Wroclaw, Poland
2. Department of Organic and Physical Chemistry, West Pomeranian University of Technology, 70-061, Szczecin, Poland
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.jpca.6b11926
Reference38 articles.
1. 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
2. Relationship between substituent effect and aromaticity – Part III: naphthalene as a transmitting moiety for substituent effect
3. Substituent effect on local aromaticity in mono and di-substituted heterocyclic analogs of naphthalene
4. peri Interaction in Naphthalene Derivatives
5. Interactions between Functional Groups. Part III. The Structure ofN,N-Dimethyl-8-nitro-1-naphthaleneamine in Seven Crystalline Environments
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1. Investigation of intramolecular hydrogen bonding in naphthoquinone derivatives by quantum chemical calculations;Journal of Physical Organic Chemistry;2022-07-22
2. Substituent effects of nitro group in cyclic compounds;Structural Chemistry;2020-09-04
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