A boron-dipyrromethene-based fluorescent probe for colorimetric and ratiometric detection of sulfite

J Agric Food Chem. 2011 Nov 23;59(22):11935-9. doi: 10.1021/jf2032928. Epub 2011 Oct 24.

Abstract

BODIPY-Le, a colorimetric and ratiometric fluorescent probe based on boron-dipyrromethene for selective detection sulfite ion, was investigated. Boron-dipyrromethene levulinyl ester (BODIPY-Le) is composed of an indole-based BODIPY dye and the levulinyl protective group, which could be easily and selectively deprotected by sulfites. As a result, the absorption and emission spectra show a dramatic red shift, and the development of a colorimetric and ratiometric fluorescent sulfite probe could be achieved. Besides, BODIPY-Le also exhibited prominent turn-on or turn-off type fluorogenic signaling toward sulfite ions once excited at 510 and 620 nm, respectively.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Boron / chemistry
  • Boron Compounds / chemistry
  • Colorimetry / methods*
  • Fluorescent Dyes / chemistry
  • Porphobilinogen / analogs & derivatives
  • Porphobilinogen / chemistry
  • Spectrometry, Fluorescence / methods*
  • Sulfites / analysis*

Substances

  • 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene
  • Boron Compounds
  • Fluorescent Dyes
  • Sulfites
  • dipyrromethene
  • Porphobilinogen
  • Boron