Abstract
3-(Benzoimidazol-2-yl)-2-phenylimino-2H-chromenes were synthesized. The protolytic equilibrium constants in 50% ethanol were determined. The correlations of the pK a values for the compounds in the ground and excited states and the PM3-calculated heats of formation with the σ+ constants of substituents were established. The nitrogen atom of the benzoimidazole fragment is the center of protonation in the studied compounds.
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Karasev, A.A., Lukatskaya, L.L., Rubtsov, M.I. et al. Synthesis, acid-base and spectral properties of 3-(benzoimidazol-2-yl)-2-phenylimino-2H-chromenes. Russian Chemical Bulletin 51, 2070–2073 (2002). https://doi.org/10.1023/A:1021616027620
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DOI: https://doi.org/10.1023/A:1021616027620