Abstract
A study has been made of the acidic ionization, structural conversions, and prototropic tautomerism of rhodamine chromogens in methanol and dimethyl sulfoxide, using IR,13C NMR, and electronic spectroscopy. The lactone structure has been established for the colorless form of rhodamines in DMSO. For rhodamine B in mixtures of water with DMSO, the lactone/zwitterion ratio has been estimated.
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V. I. Vernadskii Institute of Geochemistry and Analytical Chemistry, Russian Academy of Sciences, Moscow 117975. Khar'kov State University, Khar'kov 310077. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 3, pp. 512–521, March, 1992.
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Mchedlov-Petrosyan, N.O., Fedorov, L.A., Sokolovskii, S.A. et al. Structural conversions of rhodamines in solution. Russ Chem Bull 41, 403–409 (1992). https://doi.org/10.1007/BF00863052
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DOI: https://doi.org/10.1007/BF00863052