Abstract
Methoxy-substituted 2-(2-tosylaminophenyl)-4H-3,1-benzoxazin-4-one and 2-phenyl-4H-3,1-benzoxazin-4-one were synthesized. Their UV, IR, and luminescence spectra were studied. The position of the methoxy group affects the strength of the intramolecular hydrogen bond (IHB). The luminescence properties of methoxy-substituted 2-(2-tosylaminophenyl)-4H-3,1-benzoxazin-4-ones are associated with the strength of the IHB. The luminescence maximum is shifted to the short-wave region with strengthening of the IHB, and the luminescence intensity increase simultaneously.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1028–1032, August, 1971.
The authors thank Yu. S. Ryabokobylko and A. O. Zisman for measuring the absorption spectra in the IR and UV regions.
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Loseva, M.V., Bolotin, B.M. & Krasovitskii, B.M. 4H-3,1-Benzoxazin-4-ones methoxy-substituted 2-(2-arenesulfonylaminophenyl)-4H-3,1-benzoxazin-4-ones. Chem Heterocycl Compd 7, 964–967 (1971). https://doi.org/10.1007/BF00477372
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DOI: https://doi.org/10.1007/BF00477372