Abstract
The chemical shifts of the protons in the proflavine and acridine orange molecules in aqueous solution were measured by 1H NMR spectroscopy. The equilibrium constants for the association of the molecules and the chemical shifts of the protons in the monomers and associates were obtained from the concentration dependence of the proton chemical shifts. The most probable structures for the dimers of the dyes were calculated on the basis of the obtained chemical shifts, and a comparative analysis was made.
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Translated from Teoreticheskaya i Éksperimental'naya Khimiya, Vol. 23, No. 3, pp. 373–376, May–June, 1987.
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Veselkov, A.N., Dymant, L.N. & Dreval', S.S. Investigation of the self-association of proflavine and acridine orange molecules in aqueous solution by 1H NMR. Theor Exp Chem 23, 346–350 (1987). https://doi.org/10.1007/BF00531393
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DOI: https://doi.org/10.1007/BF00531393