Abstract
A novel dual-response fluorescence probe (XBT-CN) was developed by using a fluorescence priming strategy for quantitative monitoring and visualization of hydrazine (N(2)H(4)) and hypochlorite (ClO(-)). With the addition of N(2)H(4)/ClO(-), the cleavage reaction of C=C bond initiated by N(2)H(4)/ClO(-) was transformed into corresponding hydrazone and aldehyde derivatives, inducing the probe XBT-CN appeared a fluorescence "off-on" response, which was verified by DFT calculation. HRMS spectra were also conducted to confirm the sensitive mechanism of XBT-CN to N(2)H(4) and ClO(-). The probe XBT-CN had an obvious fluorescence response to N(2)H(4) and ClO(-), which caused a significant color change in unprotected eyes. In addition, the detection limits of XBT-CN for N(2)H(4) and ClO(-) were 27 nM and 34 nM, respectively. Interference tests showed that other competitive analytes could hardly interfere with the detection of N(2)H(4) and ClO(-) in a complex environment. In order to realize the point-of-care detection of N(2)H(4) and ClO(-), an XBT-CN@hydrogel test kit combined with a portable smartphone was developed. Furthermore, the portable test kit has been applied to the detection of N(2)H(4) and ClO(-) in a real-world environment and food samples, and a series of good results have been achieved. Attractively, we demonstrated that XBT-CN@hydrogel was successfully applied as an encryption ink in the field of information security. Finally, the probe can also be used to monitor and distinguish N(2)H(4) and ClO(-) in living cells, exhibiting excellent biocompatibility and low cytotoxicity.