Axially-chiral boramidine for detailed (chir)optical studies.
Nidal SalehEstefanía Sucre-RosalesFrancesco ZinnaCéline BesnardEric VautheyJérôme LacourPublished in: Chemical science (2024)
The inclusion of boron atoms into chiral π-conjugated systems is an effective strategy to unlock unique chiroptical properties. Herein, the preparation and characterization of a configurationally stable axially-chiral boramidine are reported, showcasing absorption in the UV domain, deep-blue fluorescence ( Φ up to 94%), and ca. |10 -3 | g abs and g lum values. Detailed photophysical studies and quantum-chemical calculations clearly elucidate the deactivation pathways of the emissive state to triplet excited states, involving increased spin-orbit coupling between the lowest singlet excited state and an upper triplet state.