4-(5-Arylvinyl-2-oxazolyl)- and 4-(5-arylbutadienyl-2-oxazolyl)-naphthalic anhydrides
- 28 Downloads
4-(5-Arylvinyl-2-oxazolyl)- and 4-(5-arylbutadienyl-2-oxazolyl)naphthalic anhydrides were synthesized by a phosphonate modification of the Wittig reaction from 4-(5-bromomethyl-2-oxazolyl)naphthalic anhydride. The structures of the aryl radicals and the steric hindrance created by some of them have a substantial effect on the absorption and luminescence of these compounds in solution. The introduction of each of the vinylene groups between the aryl and heterocyclic radicals causes approximately identical shifts in the spectra, but the Stokesian shift increases. These effects are reinforced considerably under the influence of electron-donor substituents in the aryl radical. The luminescence maxima of the investigated substances range from 515 to 710 nm, and the absolute quantum yields range from 0.12 to 0.51.
KeywordsOrganic Chemistry Vinylene Anhydride Quantum Yield Steric Hindrance
Unable to display preview. Download preview PDF.
- 1.B. M. Krasovitskii, S. E. Kovalev, and V. M. Shershukov, Khim. Geterotsikl. Soedin., No. 10, 1331 (1973).Google Scholar
- 2.B. M. Krasovitskii, S. E. Kovalev, and V. M. Shershukov, Khim. Geterotsikl. Soedin., No. 8, 1049 (1974).Google Scholar
- 3.D. G. Pereyaslova, S. E. Kovalev, and D. A. Zvyagintseva, in: Scintillators and Organic Luminophores [in Russian], Kharkov (1972), p. 131.Google Scholar
- 4.L. L. Nagornaya, R. N. Nurmukhametov, L. Ya. Kalkes, and L. V. Shubina, Izv. Akad. Nauk SSSR, Ser. Fiz., 37, 748 (1963).Google Scholar
- 5.E. Lippert, Z. Phys. Chem., 2, 328 (1954).Google Scholar
- 6.A. S. Cherkasov, Zh. Fiz. Khim., 29, 2209 (1955).Google Scholar
- 7.V. M. Shershukov, E. G. Yushko, and B. M. Krasovitskii, Zh. Vsesoyuzn. Khim. Obshchestva, 31, 584 (1976).Google Scholar