Neo-fused hexaphyrin: A molecular puzzle containing an N-linked pentaphyrin

Document Type

Article

Publication Date

1-1-2014

Abstract

The first neo-confused hexaphyrin(1.1.1.1.1.0) was synthesized by oxidative ring closure of a hexapyrrane bearing two terminal ``confused'' pyrroles. The new compound displays a folded conformation with a short interpyrrolic C center dot center dot center dot N distance of 3.102 angstrom, and thus it readily underwent ring fusion to afford a neo-fused hexaphyrin with an unprecedented 5,5,5,7-tetracyclic ring structure. Furthermore, coordination of Cu-II triggered a ring opening/contracting reaction to afford a Cu-II complex of an N-linked pentaphyrin derivative. The roles of reactive N-C bonds in the porphyrinoid macrocycles were demonstrated.

Keywords

Fused-ring systems, hexaphyrins, macrocycles, pentaphyrins, porphyrinoids

Publication Title

Angewandte Chemie International Edition

Volume

53

Issue

51

Publisher

John Wiley & Sons

Publisher Location

BOSCHSTRASSE 12, D-69469 WEINHEIM, GERMANY

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