Substituents and Environment Influences on Aromaticity of peri- and para-Substituted Naphthalenes
Author:
Affiliation:
1. Faculty of Pharmacy, Wroclaw Medical University, Borowska 211a, 50-556 Wroclaw, Poland
2. Institute of Chemistry and Environmental Protection, 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/jp5047672
Reference33 articles.
1. peri Interaction in Naphthalene Derivatives
2. Non-bonded intra-molecular interactions in 1,8-disubstituted naphthalenes with a cyano group as the electrophilic substituent
3. peri-Interactions in Naphthalenes, 14 [1]. Pyramidalization versus Planarization at Nitrogen in 8-Dialkylamino-naphth-1-yl Compounds as a Measure of peri Bond Formation
4. The molecular structures and electron distributions of the 1,8-bis-(dimethylamino)-naphthalenes, studied by density functional and ab initio MP2 calculations
5. Three examples of naphthalene proton sponges with extreme or unusual structural parameters. General view on factors influencing proton sponge geometry
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1. Excited‐State Dynamics in Segregated Donor‐Acceptor Stacks Versus a Peri‐Bisdonor‐Acceptor System;Chemistry – A European Journal;2024-08-20
2. N,N‐ and N,O‐6‐membered Ring peri ‐Annelation in Naphthalene. Is it a Heteroring or merely a peri ‐ Heterobridge?;ChemistrySelect;2021-02
3. Aromaticity of peri- and para-Substituted Naphthalene-1-carbaldehyde. Comparison with 1-Nitronaphthalene;The Journal of Physical Chemistry A;2017-03-23
4. 1 H and 13 C NMR spectral assignments of novel adamantyl and di-adamantyl derivatives of 1,2-dihydroxynaphthalenes, 1,8-dihydroxynaphthalenes, 2,3-dihydroxynaphthalenes, 2,6-dihydroxynaphthalenes and 2,7-dihydroxynaphthalenes;Magnetic Resonance in Chemistry;2016-07-29
5. Cyclic π-electron delocalization in non-planar linear acenes;Physical Chemistry Chemical Physics;2016
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