Reactivity of highly unsaturated molecules – investigation of the photo-oxidation of Bitumen & Chemistry of propargyl carbocations

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dc.contributor.advisor Clyburne, Jason A. C. (Jason Alexander Cameron), 1968-
dc.contributor.advisor Masuda, Jason Douglas, 1977-
dc.creator Laprade, Matthew Joshua Joseph
dc.date.accessioned 2024-10-11T16:13:44Z
dc.date.available 2024-10-11T16:13:44Z
dc.date.issued 2020-12-16
dc.identifier.uri https://library2.smu.ca/xmlui/handle/01/32047
dc.description 1 online resource (viii, 125, ix, 222 pages) : colour illustrations charts (some colour, graphs (some colour)
dc.description Includes abstract.
dc.description Includes bibliographical references (pages 124-125, 219-222).
dc.description.abstract The contents of this thesis have been divided into two separate parts, with permission from Saint Mary’s University. Each part is to be treated as its own self-enclosed thesis, with no relation to each other, even though there may be overlaps in the underlying chemistry. <br> Investigation of the Photo-Oxidation of Bitumen - Highly unsaturated organic molecules, commonly referred to as porphyrins, within bitumen are oxidized when exposed to sunlight. These photo-oxidized porphyrins influence the chemical and physical properties of the bitumen. The generation of these oxidized porphyrins have been monitored using infrared spectroscopy (IR), nuclear magnetic resonance (NMR), gas chomatography/mass spectrometry (GCMS), and saturate, aromatic, resin and asphaltene (SARA) analyses. <br> Chemistry of Propargyl Carbocations - Highly unsaturated organic molecules are very reactive and readily undergo addition reactions. The reactivity of unsaturated molecules will be further modified by the inclusion of a carbocationic center. For instance, the reactivity of an alkyne is believed to increase with the presence of an adjacent carbocation; a structure referred to as a propargyl carbocation. The carbocation will withdraw electron density, causing the alkyne carbon to form a dipole moment and become highly reactive. We have been able to isolate several stable propargyl carbocations and made preliminary investigations into their chemistry. en_CA
dc.description.provenance Submitted by Greg Hilliard (greg.hilliard@smu.ca) on 2024-10-11T16:13:44Z No. of bitstreams: 1 Laprade_Matthew_MASTERS_2020.pdf: 10236009 bytes, checksum: a0cf28fb796c1444d7bb115839edeb48 (MD5) en
dc.description.provenance Made available in DSpace on 2024-10-11T16:13:44Z (GMT). No. of bitstreams: 1 Laprade_Matthew_MASTERS_2020.pdf: 10236009 bytes, checksum: a0cf28fb796c1444d7bb115839edeb48 (MD5) Previous issue date: 2020-12-16 en
dc.language.iso en en_CA
dc.publisher Halifax, N.S. : Saint Mary's University
dc.subject.lcsh Hydrocarbons -- Reactivity
dc.subject.lcsh Bitumen -- Oxidation
dc.subject.lcsh Bitumen -- Properties
dc.subject.lcsh Porphyrins
dc.subject.lcsh Carbocations -- Reactivity
dc.title Reactivity of highly unsaturated molecules – investigation of the photo-oxidation of Bitumen & Chemistry of propargyl carbocations en_CA
dc.title.alternative Reactivity of highly unsaturated molecules – investigation of the photo-oxidation of Bitumen
dc.title.alternative Chemistry of propargyl carbocations
dc.type Text en_CA
thesis.degree.name Master of Science in Applied Science
thesis.degree.level Masters
thesis.degree.discipline Chemistry
thesis.degree.grantor Saint Mary's University (Halifax, N.S.)
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