Year: 2025
Type: article
Abstract: Boramidine is a small water-soluble organic fluorophore that was recently introduced as a versatile building block of fluorescent probes. Herein, we show that boramidine is protonated in highly protic solvents. This behaviour explains the surprisingly large difference in the absorption spectrum reported previously when going from an organic to an aqueous environment. Transient absorption measurements reveal that the invariance of the fluorescence spectrum to the environment arises from an excited-state proton transfer to the solvent occurring a few ps after photoexcitation of the protonated boramidine. This photoacidity of boramidine is a further add-on to the polyvalence of this fluorophore.
Source: Chemical Communications
DOI: 10.1039/d5cc02043c
Institution: University of Geneva
Language: English
Subfield: Physical and Theoretical Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: hybrid
OpenAlex ID: W4410416341
