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(¤@) Pyrolytic and Photolytic Studies of o-Dimethylaminostyrylarenes and Its Derivatives (¤G) Pyrolytic Study of (2-Chlorostyryl)pyridinesSu, Li-Mei 15 July 2008 (has links)
¤@¡BFlash vacuum pyrolysis (FVP) of 2-dimethylaminostilbene and its derivatives via elimination of methyl radical followed by cyclization gave quinoline and 1-methylindole and 3-phenylquinoline and 3-phenylindole. On the other hand, Photolysis of 2-dimethylaminostilbene and its derivatives via electrocyclization gave 1-dimethylaminophenanthrene, phenanthrene, 2-(4-methoxy-phenyl)-1-methyl-1H-
quinolin-4-one and 1-methyl-1H-indol-2-yl)phenylmethanone. Photolysis of 2,4'-dimethoxystilbene in acidic sulotion gave 1,6-dimethoxypheanthrene and 1-methoxypheanthrene and ketone compound via electrocyclization followed by [1,9] hydrogen shift.
¤G¡BFVP of 2-(2-chlorostyryl)pyridine gave benzo[f]quinolin, benzo[h]quinolin, on the other hand, FVP of 4-(2-chlorostyryl)pyridine gave different benzo[h]quinolin.
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(¤@) Pyrolytic and Photolytic Studies of 2-(Dimethylamino)styrylarenes and 2-(Benzylmethylamino)styrylarenes (¤G) Pyrolytic Study of Benzoic 1,3-Dimethyl-2-indolyl AnhydridePeng, Jheng-syong 27 July 2009 (has links)
¤@.Pyrolysis of 2-(N,N-dimethylamino)styrylarenes (29a-e) and 2-(N,N- benzylmethylamino)styrylarenes (30a-f) both gave 2-(ar-2-yl)- benzo[b]arenes 35a-f, 39a-e, their isomers 36a-e, 40a-e and the other products. On the other hand, photolysis of 29a-e gave electrocyclic products 2, 57b-e and 22a-e, respectively. However photolysis of 30a-f only gave the complicated and unknown compounds.
¤G.Pyrolysis of benzoic 1,3-dimethyl-2-indolyl anhydride (54) gave (1,3-dimethylindol-2-yl)phenylmethanone (63), 1,3-dimethylindole (65) and bis(1,3-dimethylindol-2-yl)methanone (66) as the main products.
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Molecular rearrangements of photolytically generated carbocationsMladenova, Gabriela. January 2001 (has links)
Thesis (M. Sc.)--York University, 2001. Graduate Programme in Chemistry. / Typescript. Includes bibliographical references (leaves 85-90). Also available on the Internet. MODE OF ACCESS via web browser by entering the following URL: http://wwwlib.umi.com/cr/yorku/fullcit?pMQ71609.
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Kinetics and benefits of employing UV light for the treatment of aqueous ammonia in wastewaterBergese, John 13 August 2013 (has links)
Nitrogen compounds, such as aqueous ammonia, are a widespread problem in the wastewater industry as they are toxic to numerous aquatic life, cause eutrophication, and contribute to various environmental concerns. Environment Canada has mandated new wastewater regulations, limiting un-ionized ammonia discharge to 1.25 mg/L, expressed as nitrogen. This study provides insight into methods for removing nitrogen compounds, specifically aqueous ammonia, from wastewater. Two wastewater treatment technologies were compared: Ultra Violet light and an electrochemical process. These treatments were evaluated individually, as well as in combination, to determine potential synergistic effects.
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Laboratory studies of the atmospheric oxidation of dimethyl sulfide using laser flash photolysis coupled with tunable diode laser absorption spectroscopyZhao, Zhizhong 05 1900 (has links)
No description available.
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Laser flash photolysis studies of O(¹D₂) and OH(X²II) reactions of atmospheric interestStrekowski, Rafal 05 1900 (has links)
No description available.
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Laser flash photolysis studies of some halogen monoxide reactions of atmospheric interestCronkhite, Jeffrey M. 12 1900 (has links)
No description available.
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Studies of transient free radicals in solution by flash photolysis E.S.RSimpson, Nigel J. K. January 1990 (has links)
An introduction is presented to the nature of polarized and non-polarized transient spin resonance signals, produced by flash-photolysis e.s.r., followed by a description of the equipment used for experimental work. Theories of Chemically Induced Dynamic Electron Spin Polarization are reviewed and various models introduced to illustrate these concepts. A description is given of the first thorough investigation into the effect of CIDEP polarization transfer down a free radical chain and expands upon the consequences of hyperfine-dependent relaxation and the relative signs of coupling constants in various radical species. It concludes with an account of two methods of kinetic analysis which are the first practical demonstrations of their kind, and employ extension of expressions developed in earlier chapters. Studies are made of the CIDEP behaviour of radicals in high viscosity paraffins. A reassessment of previous published work is made: anomalous polarization behaviour was found to have been over-compensated for. A new method of extracting values for T<sub>1</sub> and T<sub>2,/sub> is demonstrated for strong transient e.s.r. signals. A collection of experimental data relating to the previously unexplained absorptive polarization observed in the spectrum of ketyl radicals and the longer-time phase inversion of hyperfine-dependent CIDEP is given. The operation of Triplet Mechanism CIDEP in the ketyl radical systems is ruled out and a division of radicals into geminately formed and free-encounter pairs is shown to be incapable of explaining the observed phase changes. In its place a cross-relaxational mechanism, drawing upon simultaneously generated nuclear spin polarization is advanced. Conclusions are drawn that this may account for both anomalies. Lastly a photochemical application of CIDEP is demonstrated; two different reaction intermediates are identified upon photolysis of ortho phthalaldehyde, depending upon the quenching conditions. A reaction scheme consistent with all experimental data is proposed. A brief comment upon the photo-chemistry of indan 2-one concludes this work.
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Absolute rate constants for some reactions of the triethylamine-boryl radical and the borane radical anion /Sheeller, Brad, January 1900 (has links)
Thesis (M.Sc.) - Carleton University, 2001. / Includes bibliographical references (p. 86-90). Also available in electronic format on the Internet.
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Photochemical properties of photoallergens and their dependence on human serum albuminJones, Anita Wendy January 1997 (has links)
Photoallergic compounds cause an allergy when applied to the skin and the skin is then exposed to light. Photoallergy is connected with the ability of the allergen to bind to the skin. This thesis describes much basic photochemistry of several photoallergens and has explained any differences in that photochemistry when on surfaces and in the presence of H.S.A.
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