A number of photochromic indolinespirochromenes containing a phenyl or p-methoxyphenyl substituent in the 5′ position of the indoline portion of the molecule were synthesized. The introduction of an aryl substituent in the 5′ position gives rise to a slight bathochromic shift of the longwave absorption band of the merocyanine form of the spirochromene. © 1977 Plenum Publishing Corporation.
CITATION STYLE
Gal’bershtam, M. A., Przhiyalgovskaya, N. M., Lazarenko, I. B., Kononova, V. S., & Suvorov, N. N. (1976). Synthesis and spectral characteristics of photochromic 5′-aryl- 1′, 3′, 3′-trimethyl-6-nitro-2h-chromene-2-spiro-2′-indolines. Chemistry of Heterocyclic Compounds, 12(4), 417–419. https://doi.org/10.1007/BF00480428
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