Asymmetrical Heteroatom Substitutions in the Indenofluorene Framework: Synthesis and Characterization of 4,10-Dimesitylbenzo[5,6]-s-indacene[1,2-b]thiophene and 5,11-Dimesitylbenzo[5,6]-s-indacene[1,2-b]thiophene

dc.contributor.authorO'Neal, Nathaniel
dc.date.accessioned2015-08-13T19:27:30Z
dc.date.available2015-08-13T19:27:30Z
dc.date.issued2015-06
dc.description46 pages. A thesis presented to the Department of Chemistry, Biochemistry, and the Clark Honors College of the University of Oregon in partial fulfillment of the requirements for degree of Bachelor of Science, Spring 2015.en_US
dc.description.abstractThis project describes the synthetic method for production of asymmetrical indenofluorenes. The method presented allows for broad yet selective asymmetric substitution on the indenofluorene framework and provides a basis for future asymmetric indenofluorene derivatives. As proof of concept, this project synthesized and characterized 4,10-dimesitylbenzo[5,6]-s-indacene[1,2-b]thiophene and 5,11-dimesitylbenzo[5,6]-s-indacene[1,2-b]thiophene. Asymmetrical indenofluorenes have potential use as n-type organic semiconductors. As such, the structural, optical, and electronic properties of these compounds have also been analyzed and reported. Additionally, this project led to the creation of several compounds hitherto undescribed in the literature.en_US
dc.identifier.urihttps://hdl.handle.net/1794/19155
dc.language.isoen_USen_US
dc.publisherUniversity of Oregonen_US
dc.rightsCreative Commons BY-NC-ND 4.0-USen_US
dc.subjectChemistryen_US
dc.subjectSemiconductorsen_US
dc.subjectOrganicen_US
dc.subjectN-typeen_US
dc.subjectSynthesisen_US
dc.subjectAsymmetricalen_US
dc.subjectIndenofluoreneen_US
dc.titleAsymmetrical Heteroatom Substitutions in the Indenofluorene Framework: Synthesis and Characterization of 4,10-Dimesitylbenzo[5,6]-s-indacene[1,2-b]thiophene and 5,11-Dimesitylbenzo[5,6]-s-indacene[1,2-b]thiopheneen_US
dc.typeThesis / Dissertationen_US

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