Conclusions
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1.
Depending on the nature of the heterocycle, the heterocyclic part of a spiropyran molecule may serve either as a donor or as an acceptor of electronic excitation energy.
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2.
The rate constant for the rupture of the C-O bond in the singlet excited state of the chromene part of the molecule is independent of temperature.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1520–1526, July, 1982.
The authors thank É. R. Zakhs and V. P. Martynova for synthesizing the spiropyrans.
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Dvornikov, A.S., Malkin, Y.N. & Kuz'min, V.A. Mechanism of the degradation of electronic excitation energy in photochromic spiropyrans. Russ Chem Bull 31, 1355–1359 (1982). https://doi.org/10.1007/BF00954153
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DOI: https://doi.org/10.1007/BF00954153