| Literature DB >> 24568267 |
Jean-Benoît Giguère1, Joël Boismenu-Lavoie, Jean-François Morin.
Abstract
An efficient and versatile synthetic strategy toward cruciform anthanthrene compounds using Sonogashira couplings steps was developed. Acetylenic linkers were used to effectively extend the π-conjugation of polycyclic anthanthrone and anthanthrene compounds and tune their optoelectronic properties. Structure-property relationships supported by DFT calculations indicated more effective π-conjugation along the 6,12 axis than along the 4,10 axis. These molecules displayed strong J-aggregation both in solution and in the solid state and proved to be highly photostable with reversible redox processes, which are properties of interest in materials sciences.Entities:
Year: 2014 PMID: 24568267 DOI: 10.1021/jo402674m
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354