Catalytic solid substrate room temperature phosphorimetry for the determination of trace rhamnose based on its...

Calcein (R) could not only emit strong and stable room temperature phosphorescence (RTP) on filter paper using I(-) as perturber, but also could be oxidized by H(2)O(2) to form a non-phosphorescence compound (R'), resulting in the quenching of RTP signal of R. Moreover, the ortho-hydrogen of phenolic hydroxyl in R took condensation reaction with rhamnose (Rha) to produce non-phosphorescence compound (R-Rha) causing the RTP signal of R to further quench, and R-Rha was oxidized by H(2)O(2) to form R' and Rha, bringing about the sharp RTP signal quenching of R. Thus, a new solid substrate room temperature phosphorimetry (SSRTP) for the determination of trace Rha based on its strong catalytic effect on H(2)O(2) oxidizing R has been established, with the detection limit (LD) of 7.8zgspot(-1) (corresponding concentration: 2.0×10(-17) gm l(-1), sample volume: 0.40 μl spot(-1)). This method has been applied to determine trace Rha in cigarettes and jujubes, with the results coinciding well with those determined by a high performance liquid chromatography (HPLC). The component of R-Rha also was analyzed by means of HPLC, mass spectrometer and nuclear magnetic resonance (NMR) measurements. The mechanism of catalytic SSRTP for the determination of trace Rha was discussed.