Issue 77, 2016

The role of steric hindrance in the intramolecular oxidative aromatic coupling of pyrrolo[3,2-b]pyrroles

Abstract

The presence of steric hindrance triggers different reaction pathways in the intramolecular oxidative aromatic coupling of tetraaryl-pyrrolo[3,2-b]pyrroles and leads to the formation of a fluorene moiety and a new cationic π-system linked together by a spiro carbon atom. Computational studies elegantly rationalized these results. These previously unknown functional dyes emit red light with reasonable efficiency.

Graphical abstract: The role of steric hindrance in the intramolecular oxidative aromatic coupling of pyrrolo[3,2-b]pyrroles

Supplementary files

Article information

Article type
Communication
Submitted
18 Jul 2016
Accepted
24 Aug 2016
First published
25 Aug 2016
This article is Open Access
Creative Commons BY license

Chem. Commun., 2016,52, 11539-11542

The role of steric hindrance in the intramolecular oxidative aromatic coupling of pyrrolo[3,2-b]pyrroles

M. Krzeszewski, P. Świder, Ł. Dobrzycki, M. K. Cyrański, W. Danikiewicz and D. T. Gryko, Chem. Commun., 2016, 52, 11539 DOI: 10.1039/C6CC05904J

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