Difference in pi-electron delocalization for monosubstituted olefinic and aromatic systems-Reference-Cited by-同舟云学术

Difference in pi-electron delocalization for monosubstituted olefinic and aromatic systems

Published:2016 Issue:99 Volume:6 Page:96527-96530
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Siodla T.¹²³⁴,Szatylowicz H.¹⁵⁶⁴,Varaksin K. S.⁷⁸⁹,Krygowski T. M.¹⁰¹¹¹²⁴

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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