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Issue 15, 2011
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Expanded porphyrins and aromaticity

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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


Submitted
27 Jan 2011
Accepted
18 Feb 2011
First published
14 Mar 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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