Skip to content
BY-NC-ND 3.0 license Open Access Published by De Gruyter June 2, 2014

Resonance Topology and Related Aspects of Fluoranthenoid / Fluorenoid and Indacenoid Hydrocarbon Radicals

Gordon G. Cash EMAIL logo and Jerry Ray Dias

Data on the number of resonance structures of free radical polycyclic conjugated hydrocarbons are tabulated and studied. The first examples of fluoranthenoid / fluorenoid and indacenoid polyradical systems are presented. Some comparative generalizations between benzenoid free radicals and fluoranthenoid / fluorenoid and indacenoid polyradical systems are formulated. For example, there is a tendency of these latter even-carbon nonalternant hydrocarbons to have fewer radical isomers compared to the former alternant hydracarbons. Examples where Fowler's leapfrog algorithm identifies the more stable fluorenoid anion and indacenoid dianion isomer are presented.

Received: 2002-2-5
Published Online: 2014-6-2
Published in Print: 2002-8-1

© 1946 – 2014: Verlag der Zeitschrift für Naturforschung

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Downloaded on 31.1.2023 from
Scroll Up Arrow