The inclusion of boron atoms into chiral pi-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 (phi up to 94%), and ca. |10-3| gabs and glum 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.An axially-chiral boramidine displays UV-absorption, deep-blue fluorescence (phi up to 94%), and |10-3| gabs and glum. Deactivation pathways of the emissive state to triplet excited states, involving increased spin-orbit coupling, are identified.

Axially-chiral boramidine for detailed (chir)optical studies

Zinna, Francesco;Lacour, Jérôme
2024-01-01

Abstract

The inclusion of boron atoms into chiral pi-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 (phi up to 94%), and ca. |10-3| gabs and glum 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.An axially-chiral boramidine displays UV-absorption, deep-blue fluorescence (phi up to 94%), and |10-3| gabs and glum. Deactivation pathways of the emissive state to triplet excited states, involving increased spin-orbit coupling, are identified.
2024
Saleh, Nidal; Sucre-Rosales, Estefanía; Zinna, Francesco; Besnard, Céline; Vauthey, Eric; Lacour, Jérôme
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/1237370
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