Indole‐Boron‐Difluoride Complexes with Anticancer and Fluorescence Properties

Eight indole-boron-difluoride complexes were synthesized from 2,3-arylpyridylindole derivatives via Sonogashira coupling and Larock heteroannulation. These complexes exhibited distinct photophysical properties. Solvent polarity influenced their spectral behavior showing hypsochromic absorption, bathochromic emission shifts, and aggregation-induced emission (AIE) in mixed solvents. The ¹⁹F NMR shifts and photophysical properties, including excitation, emission maxima, and Stokes shift, correlated with Hammett substituent constants highlighting electronic effects on molecular properties. The synthesized complexes exhibited a range of intramolecular charge transfer (ICT) behaviors, as evidenced by their Lippert-Mataga parameters. TD-DFT calculations aligned with experimental data, offering insight into spectroscopic behavior. Notably, the indole-boron-difluoride complex bearing a methyl ester group exhibited significant anticancer activity against HeLa cells and potential for fluorescence imaging, indicating its promise for biomedical applications in cell imaging and therapy.