meso‐Aryl [20]π Homoporphyrin: The Simplest Expanded Porphyrin with the Smallest Möbius Topology

An unstable conjugated homoporphyrin was successfully stabilized by introducing meso‐aryl substitutents. It was evident from the moderate diatropic ring current found by NMR analysis that the newly formed 20π conjugated free base and its protonated form exhibited Möbius aromatic character. Furthermo...

Full description

Saved in:
Bibliographic Details
Published in:Angewandte Chemie International Edition 2017-12, Vol.56 (49), p.15667-15671
Main Authors: Anju, K. S., Das, Mainak, Adinarayana, B., Suresh, Cherumuttathu H., Srinivasan, A.
Format: Article
Language:English
Subjects:
Aromatic compounds
Aromaticity
conjugation
coordination chemistry
Crystal structure
homoporphyrins
Möbius aromaticity
NMR
Nuclear magnetic resonance
porphyrinoids
Structural analysis
Topology
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:An unstable conjugated homoporphyrin was successfully stabilized by introducing meso‐aryl substitutents. It was evident from the moderate diatropic ring current found by NMR analysis that the newly formed 20π conjugated free base and its protonated form exhibited Möbius aromatic character. Furthermore, complexation as a ligand with an RhI ion afforded a unique binding mode and retained the Möbius aromaticity. Overall, these compounds are the smallest Möbius aromatic molecules, as confirmed by spectral and crystal‐structure analysis and supported by theoretical studies. Assessing the limits: The simplest expanded porphyrin with the smallest Möbius topology—[20]π homoporphyrin—was successfully stabilized by meso‐aryl substituents. The resulting ligands coordinated a RhI ion through an unexpected binding mode. Spectral and structural analysis confirmed the Möbius aromatic character of the free base (top right in the picture) as well as the protonated (bottom left) and metal‐coordinated states (bottom right).
ISSN:1433-7851
1521-3773
DOI:10.1002/anie.201709859