A novel coumarin–naphthalimide‐based ratiometric fluorescent probe, called XPT, was synthesized with the aim of achieving high sensitivity and anti‐interference for N 2 H 4 detection. The probe XPT consists of coumarin species and naphthalimide species, which act as the energy donor and acceptor, respectively. The phthalimide group functions as the recognition unit for N 2 H 4 . Without the presence of hydrazine, the naphthalimide remains in a non‐fluorogenic phthalimide mode, disrupting the FRET signal. However, the phthalimide group undergoes the Gabriel reaction to an amine, which induces FRET and consequently causes a shift in the emitted fluorescence from 468 to 528 nm when N 2 H 4 was added. The results of the study demonstrated that XPT exhibits high sensitivity with a limit of detection 2.2 μM, as well as selectivity. Furthermore, it is remarkable that the distribution of N 2 H 4 in real water samples can be monitored by XPT.
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Luo et al. (2024) studied this question.
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