Styryl benzoxazolium salts as environment-sensitive mitochondrial probes for imaging ferroptosis

Styryl benzoxazolium salts are promising fluorescent scaffolds, yet systematic studies on their structure-property relationships and biological applications remain limited. To address this gap, we synthesized five novel derivatives (A1-A5) bearing diverse electron-donating groups and evaluated their photophysical behavior, viscosity sensitivity, and bioimaging performance. All derivatives exhibited strong intramolecular charge transfer (ICT) character, high environmental sensitivity, and notable Stokes shifts, with A5 showing near-infrared emission and significant viscosity-dependent fluorescence enhancement (53-fold). Probes A1, A2, A4, and A5 selectively targeted mitochondria in live COS-7 cells with high Pearson correlation coefficients (PCC > 0.82), while A5 additionally enabled real-time monitoring of mitophagy and mitochondrial viscosity changes during ferroptosis. Cytotoxicity assays confirmed their biocompatibility up to 40 μM, and A5's responsiveness was validated <i>via</i> ferrostatin-1 rescue and malondialdehyde assays. These findings establish A1-A5 as structurally tunable, organelle-specific fluorophores with diagnostic potential for cellular dynamics and regulated cell death pathways. Our study is the first to explore the imaging performance and biological applications of this dye class, establishing a foundation for the rational design of advanced probes in cell biology.