Effects of solvent on the electronic absorption and fluorescence spectra of quinazolines, and determination of their ground and excited singlet-state dipole moments
β Scribed by J.J. Aaron; A. Tine; M.D. Gaye; C. Parkanyi; C. Boniface; T.W.N. Bieze
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- English
- Weight
- 843 KB
- Volume
- 47
- Category
- Article
- ISSN
- 1386-1425
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β¦ Synopsis
The electronic absorption, and fluorescence excitation and emission spectra of 11 quinaxolines have been measured at room temperature (298 K) in several solvents of different polarities (cyclohexane, dioxane, ethylether, chloroform, ethylacetate, 1-butanol, 2-propanol, ethanol, methanol, acetonitrile, dimethylformamide and dimethyl sulfoxide). The effects of the solvent upon the spectral properties are discussed. Experimental ground-state dipole moments were measured for quinazolines and were used in combination with the spectral results to evaluate their first excited singlet-state dipole moments by means of the solvatochromic shift method. The theoretical ground and excited singlet-state dipole moments for selected quinaxolines were calculated as a vector sum of the n-component (obtained by the PPP method) and the u-component (obtained from u-bond moments). A reasonable agreement was observed between the experimental and the theoretical values. Excited singlet-state dipole moments are higher than the ground-state values for most quinaxolines.
π SIMILAR VOLUMES
Three representative diphenyltriafulvenes, 4,4'-dicy.mo-1 ,2-diphenyltriafulvenc (I), hexaphenyltriapentafulvalene (II) and IO-(3,3diphenylcyclopropenyliden)-anthrone (III) have been investigated. On excitation. the dipole moment of I decreases and reverses sign, i.e., from a value of 7.9 D in the g