Issue 15, 2011
From the journal:

Chemical Communications

Expanded porphyrins and aromaticity

Atsuhiro Osuka*a  and  Shohei Saitoa  

* Corresponding authors

a Department of Chemistry, Graduate School of Science, Kyoto University, Kyoto 606-8502, Japan
E-mail: osuka@kuchem.kyoto-u.ac.jp
Fax: +81 75-753-3970
Tel: +81 75-753-4008

Abstract

meso-Aryl-substituted expanded porphyrins that are porphyrin homologues consisting of more than five pyrrolic units are a nice platform to realize diverse aromatic and antiaromatic species as well as stable radical species. They are also an ideal series to realize topologically twisted molecules with distinct Möbius aromaticity and antiaromaticity.

Graphical abstract: Expanded porphyrins and aromaticity

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Article information

DOI
https://doi.org/10.1039/C1CC10534E
Article type
Highlight
Submitted
27 Janv. 2011
Accepted
18 Febr. 2011
First published
14 Marts 2011

Chem. Commun., 2011,47, 4330-4339

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Expanded porphyrins and aromaticity

A. Osuka and S. Saito, Chem. Commun., 2011, 47, 4330 DOI: 10.1039/C1CC10534E

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