- Chiral Near-Infrared Fluorophores by Self-Promoted Oxidative Coupling of Cationic Helicenes with Amines/Enamines
Bosson, J.; Labrador, G. M.; Besnard, C.; Jacquemin, D.; Lacour, J.
Angew. Chem. Int. Ed. 2021, 60, 8733-8738
In one pot, tertiary alkyl amines are oxidized to enamines by cationic dioxa helicene, which further reacts as electrophile and oxidant to form mono or bis donor-π-acceptor coupling products. This original and convergent synthetic approach provides a strong extension of conjugation yielding chromophores that absorb intensively in far-red or NIR domains (λmax up to 791 nm) and fluoresce in the NIR as well (λmax up to 887 nm). Intense ECD properties around 790 nm with a |Δε| value up to 60 M-1 cm-1 are observed.
open archive unige:150867