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Liquid Scintillators. The Photooxidation Of 2,5-Diphenyloxazole, Margaret E. Ackerman

Chemistry and Chemical Biology ETDs

Mackay had found that prolonged ultraviolet irradiation of solutions of 2,5-diphenyloxazole (PPO) (1) in toluene resulted in the formation of an insoluble crystalline product 2 which accumulated above the meniscus; the formation of 2 was dependent upon the presence of dissolved oxygen and water in the solutions. The Compound 2 was not a simple degradation product of PPO (1); elemental analysis was compatible with the empirical formula C22H17O5N and the thermal decomposition of 2 gave equal molar amounts of carbon monoxide, benzoic acid, and dibenzamide. The study described in this dissertation was initiated to establish the structure of 2 and …

A Spectroscopic Investigation Of Electron Transfer Transitions In Osmium (Ii) Complexes., Brian J. Pankuch

Chemistry and Chemical Biology ETDs

Osmium (II) complexes containing organic coordinating ligands 2.2'-bipyridine, 1.10-phenanthroline, 2.2' .2"­terpyridine were studied spectroscopically. Syntheses were carried out by published methods, and each complex was checked by chemical analysis and thin layer chromatography. The complexes were shown to be d6 strong field systems by magnetic susceptibility measurements performed at room temperature in air.

Room temperature absorption spectra in the visible and near-ultraviolet were measured in solvents of different polarities (H₂O, MeOH, CH₃CN, DMF, CHCl₃) and solvent shifts of the band maxima of 0.3 to 3 kK were found. Low temperature (approximately 82-90°K) absorption spectra …

The Synthesis Of Some New Azabenzo[A]Pyrene And Monomethyl Azabenzo[A]Pyrene Derivatives, Richard E. Phillips

Chemistry and Chemical Biology ETDs

The synthesis of six new azabenzo[a]pyrenes was undertaken in order that the carcinogenic and carcinostatic properties of these com­pounds might be tested. The compounds thus synthesized were 4-aza­ benzo[a]pyrene (1), 5-methyl-4-azabenzo[a]pyrene (2), 12-azabenzo[a]­pyrene (3), 11-methyl-12-azabenzo [a]pyrene (4),5 -azabenzo [a]pyrene (5), and 4-methy1-5-azabenzo[a]pyrene (6).

Compounds 1 and 2 were prepared from the intermediate 4-keto-1,2,3,4-tctrahydrochrysene. The azine from this ketone was dehydro­genated and the resulting aromatic amine was both formylated and acetylated. The amides were cyclized with polyphosphoric acid in a Bischler-Napieralski cyclodchydration giving fair yields of 1 and 2. The synthesis of compounds 3 and 4 was carried out in a …