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dc.contributor.advisorMacKinnon, Craig
dc.contributor.authorSears, Wendy Ann
dc.date.accessioned2017-06-07T19:57:10Z
dc.date.available2017-06-07T19:57:10Z
dc.date.created2005
dc.date.issued2005
dc.identifier.urihttp://knowledgecommons.lakeheadu.ca/handle/2453/2819
dc.description.abstractThe field of organic conductors is multidisciplinary in nature. This thesis introduces and characterizes new conducting materials based on heterosubstituted oligothiophenes. Substituted bithiophenes, terthiophenes, and quarterthiophenes are the primary materials investigated in this thesis. Variation of the end-groups (see document) can dramatically influence the solid-state structure, giving highly conducting materials or materials with interesting electronic properties, such as a field effect current. We have synthesized a series of such oligothiophenes with a variety of functional groups, R-Tn-R’ (T = C4 H2 S) with R being either Br, I, NH2, Hx or COOH, and R’ being NO2 or Hx (CeHis). These heterosubstituted oligothiophenes contain end-groups that are complimentary electronic donors and acceptors, which will generate push-pull compounds.
dc.language.isoen_US
dc.subjectOrganic conductors
dc.subjectThiophene Synthesis
dc.subjectOligomers Synthesis
dc.subjectMolecular conductors
dc.subjectSemiconducting devices
dc.titleSynthesis and characterization of donor-acceptor oligothiophenes
dc.typeThesis
etd.degree.nameMaster of Science
etd.degree.levelMaster
etd.degree.disciplineChemistry
etd.degree.grantorLakehead University
dc.contributor.committeememberSpivak, Greg
dc.contributor.committeememberChen, Aicheng


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