New photochromic spiropyranoquinolines and their cationic derivatives have been synthesized. Quaternization of the quinoline fragment leads to significant enhancement of the thermal stability of the merocyanine isomers of these cationic spiropyrans.
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This work was carried out with the financial support of the Ministry of Education and Science of the Russian Federation (Federal Target Program "Scientific and Scientific-Pedagogical Staff of Innovative Russia" 2009-2013, State contract No. P2260), of the Grants Council of President of the Russian Federation (Grant NSh-3233.2010.3) and Russian Foundation for Basic Research (Grant 09-03-12109).
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 561-568, March, 2012.
*For Communication 34, see [1].
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Voloshin, N.A., Bezuglyi, S.O., Metelitsa, A.V. et al. Photo- and thermochromic spirans. 35.* Synthesis and photochromic properties of spiro[indoline-2,3′-pyrano[3,2-f]quinolines] and their cationic derivatives. Chem Heterocycl Comp 48, 525–531 (2012). https://doi.org/10.1007/s10593-012-1025-z
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DOI: https://doi.org/10.1007/s10593-012-1025-z