Understanding the molecular switching properties of octaphyrins
Author:
Affiliation:
1. Eenheid Algemene Chemie (ALGC)
2. Vrije Universiteit Brussel (VUB)
3. 1050 Brussels
4. Belgium
5. Sorbonne Universités
6. UPMC Univ Paris 06
7. UMR 7616
8. Laboratoire de Chimie Théorique
9. Paris
Abstract
Triggering Hückel–Möbius topological and aromaticity switches in octaphyrins by protonation and redox reactions.
Funder
Fonds Wetenschappelijk Onderzoek
Vrije Universiteit Brussel
Publisher
Royal Society of Chemistry (RSC)
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Link
http://pubs.rsc.org/en/content/articlepdf/2016/CP/C5CP07413D
Reference106 articles.
1. P. J. Garratt , Aromaticity, John Wiley & Sons, New York, 1986
2. V. I. Minkin , M. N.Glukhovtsev and B. Y.Simkin, Aromaticity and Antiaromaticity: Electronic and Structural Aspects, John Wiley & Sons, New York, 1994
3. Introduction: Aromaticity
4. Spherical Aromaticity: Recent Work on Fullerenes, Polyhedral Boranes, and Related Structures
5. Homoconjugation/Homoaromaticity in Main Group Inorganic Molecules
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