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dc.contributor.advisorKaye, Howard
dc.creatorChang, Sing-Hsiung
dc.date.accessioned2020-01-08T18:21:49Z
dc.date.available2020-01-08T18:21:49Z
dc.date.created1973
dc.date.issued1972
dc.identifier.urihttps://hdl.handle.net/1969.1/DISSERTATIONS-182145
dc.description.abstractIn order to synthesize the desired monomer, 1-vinyluracil, a new convenient N-vinylation reaction was first developed as follows. [see PDF for diagram] It was found that using some of the following techniques and combinations thereof, the cyclopolymerization of 1-vinyluracil could be completely repressed. a. polymerization at low temperature b. polymerization at high concentration of monomer c. polymerization in the solid state d. polymerization of negatively charged monomers e. polymerization of monomers containing bulky substituents. ...en
dc.format.extent135 leavesen
dc.format.mediumelectronicen
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.rightsThis thesis was part of a retrospective digitization project authorized by the Texas A&M University Libraries. Copyright remains vested with the author(s). It is the user's responsibility to secure permission from the copyright holder(s) for re-use of the work beyond the provision of Fair Use.en
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/
dc.subjectChemistryen
dc.titleNucleic acid analogs synthesis and properties of poly(1-vinyluracil)en
dc.typeThesisen
thesis.degree.disciplineChemistryen
thesis.degree.grantorTexas A&M Universityen
thesis.degree.nameDoctor of Philosophyen
thesis.degree.levelDoctoralen
dc.contributor.committeeMemberAnthony, R. G.
dc.contributor.committeeMemberMeyer, Edgar A.
dc.type.genredissertationsen
dc.type.materialtexten
dc.format.digitalOriginreformatted digitalen
dc.publisher.digitalTexas A&M University. Libraries


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