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dc.contributor.advisorPiers, Warren E.
dc.contributor.authorMorgan, Matthew Michael
dc.date2019-11
dc.date.accessioned2019-07-10T18:23:51Z
dc.date.available2019-07-10T18:23:51Z
dc.date.issued2019-07-09
dc.identifier.citationMorgan, M. M. (2019). Boron-Nitrogen Analogues of Indene Containing Hydrocarbons (Unpublished doctoral thesis). University of Calgary, Calgary, AB.en_US
dc.identifier.urihttp://hdl.handle.net/1880/110608
dc.description.abstractBoron-nitrogen (BN) containing polycyclic aromatic hydrocarbons represent an important class of compounds of fundamental and applied interest. Despite their prevalence in main group chemistry, there remain few ways to efficiently synthesize large quantities of BN containing aromatic species. We developed a method for the preparation of 3-bora-9aza-indene heterocycles based on zirconocene mediated functionalization of the ortho-CH bonds of pyridines. Unlike other methods, the boron center in these heterocycles remains functionalized with a chloride ligand allowing the compounds to be further elaborated through halide abstraction or reduction. The utility of the method was demonstrated by applying it towards the preparation of 1,5-dibora-4a,8a-diaza BN analogs of the intriguing hydrocarbon s-indacene starting from 2,5-dimethylpyrazine. This allowed us to experimentally and computationally compare the BN doped derivative to the all-carbon analogue, providing new knowledge on the effect of main group substitutions on bonding in aromatic compounds. The developed synthetic method also provided us access to a new BN doped indenide species in large scale that allowed for its reactivity to be examined in depth. It was found that the reactivity of the nucleophilic indenide depended on which electrophile it was treated with. This divergent reactivity was investigated through reactions with alkyl halides and carbon dioxide and the mechanisms determined were supported through computational methods. Inspired by the properties of the indacene species, we targeted derivatives of BN doped dihydroindeno[1,2-b]fluorene. They were synthesized via electrophilic borylation, a mildly air-sensitive technique, and the end products were handled readily under atmospheric conditions. Through transmetallation via diarylzinc reagents a series of derivatives were synthesized which show broad absorption profiles and frontier energy levels amenable to their use in organic solar cell devices. Exploratory device parameters were studied and show moderate results with PCEs reaching 2% showing the possibility of molecules containing this framework in organic electronic devices.en_US
dc.language.isoengen_US
dc.rightsUniversity of Calgary graduate students retain copyright ownership and moral rights for their thesis. You may use this material in any way that is permitted by the Copyright Act or through licensing that has been assigned to the document. For uses that are not allowable under copyright legislation or licensing, you are required to seek permission.en_US
dc.subjectBoronen_US
dc.subjectMain-groupen_US
dc.subject.classificationEducation--Sciencesen_US
dc.subject.classificationEngineering--Chemicalen_US
dc.titleBoron-Nitrogen Analogues of Indene Containing Hydrocarbonsen_US
dc.typedoctoral thesisen_US
dc.publisher.facultyScienceen_US
dc.publisher.institutionUniversity of Calgaryen
thesis.degree.nameDoctor of Philosophy (PhD)en_US
thesis.degree.disciplineChemistryen_US
thesis.degree.grantorUniversity of Calgaryen_US
dc.contributor.committeememberRoesler, Roland
dc.contributor.committeememberSutherland, Todd C.
dc.contributor.committeememberHubert, Casey R. J.
dc.contributor.committeememberGilroy, Joe B.
ucalgary.item.requestcopytrueen_US


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University of Calgary graduate students retain copyright ownership and moral rights for their thesis. You may use this material in any way that is permitted by the Copyright Act or through licensing that has been assigned to the document. For uses that are not allowable under copyright legislation or licensing, you are required to seek permission.