The synthesis and characterization of a highly photostable bromo-substituted BODIPY dye (I) fused-ring-expanded with thienopyrrole moieties is reported. The results of MTT assays and flow cytometric analyses in living HeLa cells demonstrate that I has a high singlet oxygen quantum yield (ΦΔ = 0.63) and exhibits photocytotoxicity upon irradiation in the NIR region making it potentially suitable for use in PDT.

The synthesis of a novel aza-BODIPY dye functionalized with fused pyrazine rings, suitable for use as a selective colorimetric and fluorometric sensor for NH(4)(+), is outlined. In addition to significant fluorescence quenching, an obvious colorimetric change from green to red-pink is observed enabling facile "naked-eye" detection of NH(4)(+).