| Literature DB >> 28949037 |
Henrik Gotfredsen1, Freja Eilsø Storm1, Alberto Viñas Muñoz1, Marco Santella1, Anders Kadziola1, Ole Hammerich1, Kurt V Mikkelsen1, Mogens Brøndsted Nielsen1.
Abstract
Boron subphthalocyanines comprised of three isoindole units bridged by aza-linkages are attractive light harvesters on account of their intense low-energy absorptions. Herein, we present a class of related compounds, in which one or two isoindole units are substituted for thieno[3,4-c]pyrrole units - thieno-fused subporphyrazines. Such changes have remarkable consequences for the optical properties, as was revealed by combined experimental and theoretical studies. Thus, we find that the lowest-energy absorptions cover a much broader region with a significantly redshifted end-absorption and without compromising the absorption intensities. Thieno-fused subporphyrazines also underwent more readily oxidation and reduction, indicating an increased HOMO energy and decreased LUMO energy. In addition, they were found to readily co-crystallize with Buckminsterfullerene, C60 . Altogether, these findings render this new class of chromophores attractive candidates for light-harvesting applications.Entities:
Keywords: aromaticity; chromophores; fullerenes; subphthalocyanines; thiophenes
Year: 2017 PMID: 28949037 DOI: 10.1002/chem.201704551
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236