Reichardt's dye: The NMR story of the solvatochromic betaine dye

Michal Afri, Hugo E. Gottlieb, Aryeh A. Frimer

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Reichardt's dye, 2,6-diphenyl-4-(2,4,6-triphenyl-1-pyridinio)phenolate (1), has a very large negative solvatochromism in the long wavelength absorption in the UV-vis spectrum when going from nonpolar to polar solvents. This shift provides the basis of the important and widely used ET(30) scale of solvent polarity. While many papers have investigated the properties of this dye, only a few describe the 1H and 13C NMR assignments in any detail. We report herein, our detailed analysis of the proton and carbon chemical shift assignments for this molecule based on 1D and 2D NMR measurements, as well as those of the protonated and methoxy derivatives 2 and 3, respectively. Much to our surprise, some of the critical chemical shift values we observed were significantly different from those previously reported. In addition, we discovered a good correlation not only between the solvent polarity and the chemical shifts of carbons C1 and C4 of Reichardt's dye (1), but also between the concentration of the dye and these chemical shifts.

Original languageEnglish
Pages (from-to)128-134
Number of pages7
JournalCanadian Journal of Chemistry
Volume92
Issue number2
DOIs
StatePublished - Feb 2014

Keywords

  • NMR chemical shifts
  • Reichardt's dye
  • Solvatochromism
  • Solvent effect

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