Indole-, benzofuran- and benzothiophene-containing analogues of ceramidonines and fused 3,9-diazaperylenes: Synthesis and physicochemical properties of these new polycyclic azaarenes
Ceramidonine analogues and fused 3,9-diazaperylenes were synthesised from aminoanthraquinones and 2-iodinated heteroaromatics by a copper-promoted N -arylation-cyclisation sequence. Their photophysical properties, determined experimentally and analysed through computation, revealed either efficient photosensitisers or fluorescent compounds, respectively.
Authors
- Ludmilla Verrieux
- William Erb (ORCID: https://orcid.org/0000-0002-2906-2091)
- Nicolas Richy
- Arnaud Fihey (ORCID: https://orcid.org/0000-0003-1874-0499)
- Nicolas Mast (ORCID: https://orcid.org/0000-0002-4648-3883)
- Boris Le Guennic (ORCID: https://orcid.org/0000-0003-3013-0546)
- Florence Mongin (ORCID: https://orcid.org/0000-0003-3693-8861)
- Jean Pierre Hurvois
- Olivier Mongin
- Thierry Roisnel
Institutions
- Centre National de la Recherche Scientifique (FR)
- Institut des Sciences Chimiques de Rennes (FR)
- Université de Rennes (FR)
Publication Details
- Journal
- Dyes and Pigments
- Published
- 2024-12-21
- DOI
- https://doi.org/10.1016/j.dyepig.2024.112612
- Citations
- 1
- Primary Topic
- Synthesis and Biological Evaluation
- Type
- article
- Field-Weighted Citation Impact
- 0.25
Funders
- European Regional Development Fund