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Upscale synthesis of symmetrical and unsymmetrical monomers towards bridge triflouromethylated poly (p-phenylenevinylene) and theoretical NMR studies
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Pinto, Jean Pierre. Upscale synthesis of symmetrical and unsymmetrical monomers towards bridge triflouromethylated poly (p-phenylenevinylene) and theoretical NMR studies. Retrieved from https://doi.org/doi:10.7282/T36973S8

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TitleUpscale synthesis of symmetrical and unsymmetrical monomers towards bridge triflouromethylated poly (p-phenylenevinylene) and theoretical NMR studies
NamePinto, Jean Pierre (author); Burke, Luke A. (chair); Roche, Alex J. (internal member); Arbuckle-Keil, Georgia A. (internal member); Rutgers University; Camden Graduate School
Date Created
Other Date2008-05 (degree)
SubjectChemistry, Monomers, Polymers, Polymerization, Nucleophilic reactions
Extentviii, 64 p. : ill. (some col.)
DescriptionThe objective of this research is to up scale the synthesis of previously reported symmetrical and unsymmetrical trifluoromethylated monomers in sufficiently high amounts for the synthesis and characterization of bridge substituted poly (p-phenylene) vinylene polymers. Theoretical NMR calculations are also made to differentiate between diastereomers produced during synthesis. The preliminary polymerization reactions yielded optimistic results but insufficient material was used for proper polymerization, characterization, and isolation. The monomers prepared are shown in Table 1.
NoteM.S.
NoteIncludes bibliographical references (p. 63-64).
Noteby Jean Pierre Pinto
Genretheses, ETD graduate
Persistent URLhttps://doi.org/doi:10.7282/T36973S8
Languageeng
CollectionCamden Graduate School Electronic Theses and Dissertations
Organization NameNjNbRU, Rutgers, The State University of New Jersey
RightsThe author owns the copyright to this work.
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