A novel fluorescence probe based on triphenylamine Schiff base for bioimaging and responding to pH and Fe3

Mater Sci Eng C Mater Biol Appl. 2017 Mar 1:72:551-557. doi: 10.1016/j.msec.2016.11.108. Epub 2016 Dec 5.

Abstract

A novel fluorescence probe 1 based on triphenylamine was synthesized and characterized by NMR, IR, high resolution mass spectrometry and elemental analysis. Its fluorescence was quenched when pH below 2. There was a linear relationship between the fluorescence intensity and pH value ranged from 2 to 7. And its fluorescence emission was reversibility in acidic and alkaline solution. Furthermore, it exhibited remarkable selectivity and high sensitivity to Fe3+ and was able to detect Fe3+ in aqueous solution with low detection limit of 0.511μM. Job plot showed that the binding stoichiometry of 1 with Fe3+ was 1:1. Further observations of 1H NMR titration suggested that coordination interaction between Fe3+ and nitrogen atom on CN bond promoted the intramolecular charge transfer (ICT) or energy transfer process causing fluorescence quenching. Additionally, 1 was also able to be applied for detecting Fe3+ in living cell and bioimaging.

Keywords: Bioimaging; Fluorescence probe; Schiff base; Triphenylamine.

MeSH terms

  • Benzidines / chemistry*
  • Ferric Compounds / analysis
  • Ferric Compounds / chemistry*
  • Fluorescent Dyes / chemistry*
  • HeLa Cells
  • Humans
  • Hydrogen-Ion Concentration
  • Ions / chemistry
  • Magnetic Resonance Spectroscopy
  • Metals / chemistry
  • Schiff Bases / chemistry*
  • Spectrometry, Fluorescence

Substances

  • Benzidines
  • Ferric Compounds
  • Fluorescent Dyes
  • Ions
  • Metals
  • Schiff Bases
  • tetraphenylbenzidine