Axially-chiral boramidine for detailed (chir)optical studies.

ABSTRACT: 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.

SUBMITTER: Saleh N 

PROVIDER: S-EPMC11062121 | biostudies-literature | 2024 May

REPOSITORIES: biostudies-literature