Abstract
The absorption and luminescence spectra of a series of 4,7-diaminocoumarins have been investigated in ethanol and acetonitrile solution. The pka I and pka II values for several of the compounds have been measured. It has been found that the site of primary protonation is the nitrogen atom in the 7-position, and that the second protonation reaction occurs at the lactone oxygen atom. The effects of steric and electronic factors on the spectral-luminescence and acid-base characteristics of these compounds are discussed.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1610–1618, December, 1990.
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Karandashova, L.A., KirpichËnok, M.A., Yufit, D.S. et al. Spectral-luminescence and acid-base properties of 4,7-diaminocoumarins. Chem Heterocycl Compd 26, 1338–1345 (1990). https://doi.org/10.1007/BF00473960
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DOI: https://doi.org/10.1007/BF00473960