| Popis: |
Dibenzofurans, a dibenzothiophene, and carbazoles, each substituted with a 2-benzoxazolyl group as well as an ortho-hydroxyl group, were synthesized to produce fluors with fluorescence due to excited-state intramolecular proton-transfer. The orientations for Friedel-Crafts acylation of 3-methoxydibenzothio-phene and of the analogous carbazole were determined. The fluors displayed absorption peaks in the 330–385 nm region with molar extinction coefficients up to 57,000. Fluorescence quantum efficiencies of 0.17–0.44 were obtained at wavelengths that had peak values from 540–600 nm. The fluors are of potential use as wavelength shifters in scintillating polystyrene fibers. |
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