The yield of singlet oxygen (@lo, ) in quenching of the triplets of 1.2.5.6dibenzanthracene. 1,2-benznnthncene. authracene. pyranthrene and duroquinone by oxygen has been studied using the laser photolysis technique. It ~3s found that in toluene @to2 = 1.0 + 0.1 and the quenching occurs via the ener
Solvent effects on the thioxanthone triplet quenching by vinyl monomers
β Scribed by J.P. Fouassier; P. Jacques; M.V. Encinas
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- English
- Weight
- 319 KB
- Volume
- 148
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
The quenching rate constants for the deactivation of triplet thioxanthone by methyl methacrylate and N-vinyl-2-pyrrolidone undergo a drastic decrease when the solvent polarity increases. This variation is represented by the ti, (Y, B scale of solvent polarity. The contribution to this solvent effect of vibronic coupling between nearby na* and XA* states of thioxanthone triplets is considered.
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Fluorescence quenching of anthracene by iodide ions in ethanol and propanol solutions in the temperature range 293-333 K was investigated under stationary conditions. The fluorescence quenching can be satisfactorily described using Marcus-type theory. Analysis of the experimental data indicates the
Free-radical copolymerizations of vinyl acetate (VAc Ο M 1 ) and other vinyl esters (Ο M 2 ) including vinyl pivalate (VPi), vinyl 2,2-bis(trifluoromethyl)propionate (VF6Pi), and vinyl benzoate (VBz) with fluoroalcohols and tetrahydrofuran (THF) as the solvents were investigated. The fluoroalcohols
Triplet quenching of 3-methyllumiflavin, thionine and thiopyronine by electron transfer from NO2 and N3 in acetonitrile, methanol and water was investigated by flash spectroscopy. The radical yield is systematically lower for N3 than for NO2, explicable by the different spin-orbit coupling propertie