of Fe³⁺. A RhB-EDA molecule itself is colorless and has no fluorescence emission in an alcohol solution. When Fe³⁺ was added, the lactam ring structure of the fluorescent probe opened, and the UV and fluorescence spectra changed. At the same time, the color of the mixed solution gradually deepened toward pink. Therefore, dual spectral detection and naked-eye observation of Fe³⁺ were realized. In addition, with the decrease of the pH value and the prolongation of chelating time, the ultraviolet absorbance and fluorescence emission intensity were enhanced and the color of the mixed solution deepened. The RhD-EDA fluorescent probe is simple and accurate and provides good technical support for the detection of Fe³⁺.1f:T4e3,Detection of iron ions in aqueous solutions is of significant importance because of their important role in the environment and the human body. Herein, a fluorescent rhodamine B-functionalized chitosan nanoparticles probe is reported for the efficient detection of iron ions. The chitosan nanospheres-rhodamine B (CREN) was prepared by grafting rhodamine B onto the surface of chitosan nanospheres through an amidation reaction. The as-prepared CREN fluorescent probes exhibit high fluorescence intensity under ultraviolet light. When iron ions are added to the CREN solution, they can be coordinated with weak-field ligands such as N and O on the surface of chitosan nanoparticles (CSNP) by a high-spin method. The self-assembly of Fe³⁺ on the surface of the CREN led to the generation of single electrons and the presence of high paramagnetism, resulting in fluorescence quenching. The quenching effect of Fe³⁺ on the CREN fluorescent probe can achieve the efficient detection of Fe³⁺, and the detection limit reaches 10^-5 mol/mL. Moreover, this fluorescence quenching effect of Fe³⁺ on the CREN fluorescent probe is specific, which could not be disturbed by other metal ions and counteranions.

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