“…In comparison with previously reported fluorescence sensors for Fe 3+ detection, both L1 and L2 displayed superior sensitivities in terms of detection limit, high selectivity and applicability in live cell imaging. As shown in Table , each sensor had certain advantages, such as rare interference,,,,,, low detection limits,,, single‐step synthesis, and applicability in live cell imaging ,,,,,. Another advantage of these sensors was that they could be used in aqueous media without interference from other ions, which led us to achieve the fluorescence detection of Fe 3+ in living cells at micromolar level.…”