| Literature DB >> 29938389 |
Lusheng Wang1, Bolin Li1, Chao Jiang1, Ruopei Sun1, Peizhuo Hu1, Suwen Chen2, Wangsuo Wu1.
Abstract
A new boron-dipyrromethene (BODIPY) fluorescent dye aimed at sensitively detecting hypochlorite anion (ClO-) has been designed, synthesized and characterized. The probe is comprised of a BODIPY fluorophore unit and a ClO- specific reactive group of amidoxime. The addition of hypochlorite results in a red-shift of absorption and emission spectra of the probe accompanied by a decrease of intensity and spectra changes (A500 and 1/I512) of the probe can achieve a good linearity to the concentration of ClO-. The fluorescence probe can react to ClO- rapidly (within 60 s) in a wide pH range (4-10) with high sensitivity (detection limit of 6.81 μM) and selectivity. The reaction mechanism has been proposed and confirmed by MS analysis, ClO- anion oxidizes amidoxime moiety to hydroxyl group and hydroxyl group is further oxidized to formyl group in the formation of a corresponding aldehyde compound. In addition, the probe has also been successfully applied to detect ClO- in tap water and river water samples by spiking a known amount of standard ClO-.Entities:
Keywords: Amidoxime; BODIPY; Fluorescent probe; Hypochlorite
Year: 2018 PMID: 29938389 DOI: 10.1007/s10895-018-2255-y
Source DB: PubMed Journal: J Fluoresc ISSN: 1053-0509 Impact factor: 2.217