A multifunctional fluorescent probe P based on a naphthalimide derivative for the detection of Ag⁺ and Hg²⁺ through a dual-signal was designed and characterized. P exhibited a large Stokes shift (107 nm), high selectivity, good sensitivity, and fast response time. By adjusting the testing medium and the order of reagent addition, multifunctional detection with P was achieved. The addition of Ag⁺ or Hg²⁺ to P solution in either ethanol or an ethanol–water mixture resulted in a significant quenching of fluorescence emission at 537 nm and caused a decrease in the absorbance at 440 nm accompanied by the appearance of a new absorption peak at around 340 nm, and there was an obvious color change from yellow to colorless. In contrast, the addition of other common metal ions and anions did not produce substantial spectral or color changes. The detection limit of probe P for Ag⁺ and Hg²⁺ was calculated to be 0.33 μM. The sensing mechanism was proposed and validated through MS and ¹H NMR spectrometry methods. Additionally, P demonstrated the capability to recognize Ag⁺ and Hg²⁺ in living cells with satisfactory results.

In this study, we synthesized a fluorescent material by modifying the C-2 amino group of carboxymethyl chitosan with a rhodamine B derivative, which was proposed and demonstrated using ¹H NMR and FT-IR measurements. A series of experiments including selectivity, sensitivity, reversibility, pH, and water content were conducted to investigate the fluorometric and colorimetric properties of the grafted polymer. Utilizing a Fe³⁺-induced ring-opening mechanism of the rhodamine B spirolactam, we found that the grafted polymer exhibited a highly selective fluorescence response to Fe³⁺, with enhanced fluorescence at 583 nm compared to other tested metal ions and anions, accompanied by the characteristic absorption peak of rhodamine B that appeared at 561 nm with a noticeable color change from colorless to pink, facilitating visual observation. Additionally, the modified probe, composed of carboxymethyl chitosan, was easily regenerated through treatment with EDTA.

Most reported fluorescent Al³⁺ probes rely on fluorescence signal enhancement or quenching. Since the change in fluorescence intensity is the sole detection signal, various factors such as instrumental efficiency, environmental conditions, and probe concentration can interfere with the signal output. In contrast, ratiometric probes, which utilize two emission bands for self-calibration, provide significant advantages by minimizing or eliminating these uncertainties. In this study, a naphthalimide-rhodamine based the transition between the cyclic and open-ring forms of rhodamine as an Al³⁺-selective ratiometric probe, in which chitosan was identified as an ideal bridge and biocompatibility. The design concept was that when the target metal ion was present, the fluorescence intensity of naphthalimide remained largely unchanged, serving as an internal standard. In contrast, rhodamine B was employed to label the target molecules, with its fluorescence intensity varying in accordance with the target concentration. A series of experiments were carried out to investigate the fluorometric properties of the grafted polymer P. The results demonstrated that P exhibited selective interaction with Al³⁺ among the various metals tested. Using the fluorescence intensity ratio (I_{603 nm}/I_{538 nm}) of P, a good linear relationship was achieved for Al³⁺ concentrations ranging from 1.0 to 35.0 μM with a detection limit of 0.33 μM was obtained. Meanwhile, we employed the standard addition method for the quantitative analysis and detection of Al³⁺ in commercially available bottled water and tap water, achieving an ideal recovery rate.