LAUSR

Abstract A novel luminescence phenomenon of homovanillic acid (HVA) that the excitation wavelength is longer than the emission wavelength (LExL, λex-L > λem) was observed, which was monitored by using a common spectrofluorometer with a xenon lamp as an excitation light source. As the addition of Fe3+, the intrinsic fluorescence of HVA at 310 nm was obviously quenched and a new emission peak at 424 nm emerged and raised under 557 nm excitation. The similar emission spectra of HVA-Fe3+ were also obtained at 287 nm excitation. Thus, a dual-mode ratiometric fluorescence (RF) method for detecting Fe3+ was developed based on LExL and Stokes fluorescence (SF) of HVA. The RF signals of lg(I424 nm/I310 nm) had excellent linearity with Fe3+ concentration in the range of 0.50–100 μM. Their detection limits were 0.073 μM and 0.090 μM for the LExL and SF methods, respectively. The LExL and SF methods exhibited high selectivity for detecting Fe3+, and the former has stronger anti-interference ability to Cu2+, Fe2+ etc. The proposed two methods were successfully applied for the determination of Fe3+ in actual water samples. The interaction mechanism of HVA with Fe3+ was also studied.