Difference in pi-electron delocalization for monosubstituted olefinic and aromatic systems
Author:
Affiliation:
1. Faculty of Chemistry
2. Adam Mickiewicz University
3. 61-614 Poznań
4. Poland
5. Warsaw University of Technology
6. 00-664 Warsaw
7. JSC
8. Omsk
9. Russia
10. Department of Chemistry
11. Warsaw University
12. 02-093 Warsaw
Abstract
Application of HOMA to a series of monosubstituted derivatives of cyclohexa-1,3-diene (olefinic) and benzene (aromatic) revealed an increase of the pi-electron delocalization in olefinic systems and a decrease in the case of aromatic systems.
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2016/RA/C6RA20163F
Reference16 articles.
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2. Relation between the Substituent Effect and Aromaticity
3. The substituent effect on benzene dications
4. Substituent effects in mono- and disubstituted 1,3,5,7-cyclooctatetraene derivatives in natural and planar conformations
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