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Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/8458
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dc.contributor.advisorWarkentin, J.en_US
dc.contributor.authorCameron, Audrey M.en_US
dc.date.accessioned2014-06-18T16:42:58Z-
dc.date.available2014-06-18T16:42:58Z-
dc.date.created2010-12-06en_US
dc.date.issued1972en_US
dc.identifier.otheropendissertations/3663en_US
dc.identifier.other4680en_US
dc.identifier.other1673085en_US
dc.identifier.urihttp://hdl.handle.net/11375/8458-
dc.description.abstract<p>The thermal decomposition of 2-(arylimino)-5,5diphenyl-Δ³-1,3,4-oxadiazolines, prepared by the oxidation of benzophenone 4-arylsemicarbazones by lead tetra-acetate, was studied. A possible mechanism of the decomposition is discussed in the light of a correlation between the rate constants and substituent constants. The configuration of N,5,5-trisubstituted-2-imino-Δ³-1,3,4-oxadiazolines was determined. Several new compounds, 5,5-dialkyl-Δ³-1,3,4-oxadiazolin-2-ones, were prepared by hydrolysis of 5,5-dialkyl-2-(methylimino)-Δ³-1,3,4-oxadiazolines. A literature survey of the oxidative cyclization of nitrogen-containing carbonyl derivatives, and of the thermal decomposition of cyclic azo compounds is presented.</p>en_US
dc.subjectChemistryen_US
dc.subjectChemistryen_US
dc.titleTHE SYNTHESIS AND THERMAL DECOMPOSITION OF 5,5-DIPHENYL-2-(ARYLIMINO)-Δ³-1,3,4-OXADIAZOLINES AND 5,5-DIALKYL-Δ³-1,3,4-OXADIAZOLIN-2-ONESen_US
dc.typethesisen_US
dc.contributor.departmentChemistryen_US
dc.description.degreeDoctor of Philosophy (PhD)en_US
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