1975
DOI: 10.1007/bf00614722
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Phosphorescence properties of hydroxy-substituted flavones

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Cited by 5 publications
(8 citation statements)
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“…Two fluorescence bands are observed, having ffuorescent in neutral aqueous solution a t room temperature, as it is in tetrachloromethane 20 or ethanol. 21 We noticed, however, the development of a fluorescence band a t 400-420 nm in aqueous, alcoholic acetonitrile or dioxan solution within a few minutes. The new band is found in addition to a strong Raman scatter peak a t ca.…”
Section: Resultsmentioning
confidence: 79%
“…Two fluorescence bands are observed, having ffuorescent in neutral aqueous solution a t room temperature, as it is in tetrachloromethane 20 or ethanol. 21 We noticed, however, the development of a fluorescence band a t 400-420 nm in aqueous, alcoholic acetonitrile or dioxan solution within a few minutes. The new band is found in addition to a strong Raman scatter peak a t ca.…”
Section: Resultsmentioning
confidence: 79%
“…An example of molecules of this type is the flavonols. 3-Hydroxyflavone (3-HF) and, to a lesser extent, 5-hydroxyflavone (5-HF) were extensively studied. Both steady-state fluorescence and time-resolved techniques were employed to study the ESIHT process of these two molecules.…”
Section: Introductionmentioning
confidence: 99%
“…Phosphorescence has been reported for various hydroxy-substituted flavones [40]. Phosphorescence is reported to arise from a 3(n,n*) state of these nonfluorescent molecules.…”
Section: Miscellaneousmentioning
confidence: 98%