Abstract
6-Nitro-6′,7′-tetramethylene-substituted photochromic spirochromenes were synthesized from 5-aminotetralin. In the series of compounds thus obtained the electronic effect of the substituents in the 8 position on the dark decolorization reaction is substantially more noticeable than in the corresponding series of standard spirochromenes. The spectral characteristics of the merocyanine form of the tetramethylene-substituted spirochromenes practically coincide with the. characteristics of the analogous unsubstituted compounds.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1069–1071, August, 1977.
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Gal'bershtam, M.A., Przhiyalgovskaya, N.M., Khrolova, O.R. et al. Synthesis and photochromic properties of 6′,7′-tetramethylene-substituted spirochromenes of the indoline series. Chem Heterocycl Compd 13, 859–861 (1977). https://doi.org/10.1007/BF00488910
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DOI: https://doi.org/10.1007/BF00488910