Issue 15, 2011

Expanded porphyrins and aromaticity

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

Article information

Article type
Highlight
Submitted
27 jan 2011
Accepted
18 feb 2011
First published
14 mar 2011

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

Expanded porphyrins and aromaticity

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

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