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A 1H NMR study of Nile Red solvation

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Abstract

In order to evaluate the capabilities of NMR spectroscopy for investigation of the solvatochromic effect in luminophore solutions, the 1H NMR chemical shifts of Nile Red in mixtures of solvents with different polarities (benzene, toluene, methanol) has been determined. Their dependence upon the solvent mixture composition has been revealed and binding sites for luminophore and solvent component molecules have been determined. The results of the NMR study are consistent with data on the fluorescence of Nile Red solutions in toluene-ethanol mixtures.

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Authors and Affiliations

  1. Institute of Macromolecular Compounds, Russian Academy of Sciences, Bol’shoi pr. 31, St. Petersburg, 199004, Russia

    Yu. E. Moskalenko, A. Yu. Men’shikova, N. N. Shevchenko, V. V. Faraonova & A. V. Gribanov

Authors
  1. Yu. E. Moskalenko
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  2. A. Yu. Men’shikova
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  3. N. N. Shevchenko
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  4. V. V. Faraonova
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  5. A. V. Gribanov
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Corresponding author

Correspondence to Yu. E. Moskalenko.

Additional information

Original Russian Text © Yu.E. Moskalenko, A.Yu. Men’shikova, N.N. Shevchenko, V.V. Faraonova, A.V. Gribanov, 2011, published in Khimiya Vysokikh Energii, 2011, Vol. 45, No. 3, pp. 214–218.

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Moskalenko, Y.E., Men’shikova, A.Y., Shevchenko, N.N. et al. A 1H NMR study of Nile Red solvation. High Energy Chem 45, 183–187 (2011). https://doi.org/10.1134/S0018143911030118

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  • DOI: https://doi.org/10.1134/S0018143911030118

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