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Portable and rapid hydrazine monitoring by a large Stokes shift probe with smartphone-assisted quantification: Its
Serkan Erdemir1, Mehmet Oguz1, Sait Malkondu2
1Selcuk University, Science Faculty, Department of Chemistry, Konya, 42250, Türkiye.
Environmental Pollution (Barking, Essex : 1987)
|July 4, 2026
Summary
A new fluorescent probe rapidly and selectively detects hydrazine (N2H4) by changing color from orange to blue. This simple, portable system is ideal for environmental monitoring and has shown practical applications in various samples.
Area of Science:
- Chemical Sensing
- Fluorescent Probes
- Environmental Monitoring
Background:
- Hydrazine (N2H4) is a toxic environmental pollutant requiring sensitive detection methods.
- Existing detection methods for hydrazine can be complex or lack selectivity.
- Fluorescent probes offer potential for rapid and selective analyte detection.
Purpose of the Study:
- To design and synthesize a novel phenanthroimidazole-based fluorescent probe for hydrazine detection.
- To investigate the probe's sensing mechanism, selectivity, and response time.
- To evaluate the probe's applicability in real-world environmental and biological samples.
Main Methods:
- Synthesis of a donor-π-acceptor fluorescent probe incorporating benzothiazole and arylidene nitrile units.
- Spectroscopic analysis (fluorescence spectroscopy) to study probe-analyte interactions.
- Selectivity studies against various interfering species (metal ions, anions, amines).
- Mechanistic studies involving nucleophilic addition and ICT process modulation.
- Biocompatibility assessment using cell viability assays.
- Demonstration of vapor-phase detection using TLC kits.
- Analysis of real samples (soil, plant, food) and smartphone-assisted quantification.
Main Results:
- The probe exhibited strong orange fluorescence (ICT-based) that switched to blue upon reaction with hydrazine.
- High selectivity for hydrazine over other species was observed.
- Rapid response time (∼120 s) and a low detection limit (81 nM) were achieved.
- A large Stokes shift (∼188 nm) minimized background interference.
- The sensing mechanism involves nucleophilic addition of hydrazine to the arylidene nitrile unit.
- The probe demonstrated good biocompatibility (>85% cell viability at 200 μM).
- Successful vapor-phase detection and analysis in environmental and food samples were achieved.
- Smartphone-assisted results correlated well with the ninhydrin method.
Conclusions:
- A novel, highly selective, and sensitive fluorescent probe for hydrazine detection was successfully developed.
- The probe's mechanism involves ICT modulation via nucleophilic addition.
- The developed sensing platform is suitable for rapid, portable, and reliable environmental monitoring of hydrazine.
- The probe shows potential for practical applications in diverse sample matrices and vapor-phase sensing.

