Assessing the Extent of π-Electron Delocalization in Naphtho-Annelated Fluoranthenes by Means of Topological Ring-Currents-Reference-Cited by-同舟云学术

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Assessing the Extent of π-Electron Delocalization in Naphtho-Annelated Fluoranthenes by Means of Topological Ring-Currents

Published:2019-01-22 Issue:7 Volume:123 Page:1445-1450
ISSN:1089-5639
Container-title:The Journal of Physical Chemistry A
language:en
Short-container-title:J. Phys. Chem. A

Author:

Dickens Timothy K.¹^ORCID,Mallion Roger B.²,Radenković Slavko³^ORCID

Affiliation:

1. University Chemical Laboratory, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, England, U.K.

2. School of Physical Sciences, University of Kent, Canterbury CT2 7NH, England, U.K.

3. Faculty of Science, University of Kragujevac, 12 Radoja Domanovića, 34000 Kragujevac, Serbia

Funder

Ministarstvo Prosvete, Nauke i Tehnološkog Razvoja

Publisher

American Chemical Society (ACS)

Subject

Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jpca.8b12068

Reference57 articles.

1. Local Aromaticity in Naphtho-Annelated Fluoranthenes: Can the Five-Membered Rings Be More Aromatic Than the Six-Membered Rings?

2. Correlations between Topological Ring-Currents, π-Electron Partitions, and Six-Centre Delocalisation Indices in Benzenoid Hydrocarbons

3. Quantitative approach to hückel rule the relations between the cycles of a molecular graph and the thermodynamic stability of a conjugated molecule

4. Cyclic Conjugation Energy Effects in Polycyclic π-Electron Systems

5. Pairwise energy effect of cyclic conjugation in benzo-annelated perylenes

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