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dc.contributor.advisorAdams, Emory T.
dc.creatorChen, Shu Pin
dc.date.accessioned2020-08-21T22:17:24Z
dc.date.available2020-08-21T22:17:24Z
dc.date.issued1972
dc.identifier.urihttps://hdl.handle.net/1969.1/DISSERTATIONS-776362
dc.description.abstractTrityl hexachloroantimonate has been shown to polymerize cyclic ethers readily (i.e., tetrahydrofuran, dioxolane, dioxane, etc.) No reports utilizing this cationic initiator to polymerize three member ring ethers (epoxides) exist. The polymerization mechanism of the greater than three member cyclic ethers by Ph₃CsbCl₆ are fairly well documented. Such is not the case for the three member cyclic ethers. ...en
dc.format.extent176 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.subjectMajor chemistryen
dc.titlePolymerization characteristics of styrene oxide and [alpha]-methyl styrene oxide employing the cationic initiator triphenyl methyl hexachloroantimonateen
dc.typeThesisen
thesis.degree.disciplineChemistryen
thesis.degree.grantorTexas A&M Universityen
thesis.degree.nameDoctor of Philosophyen
thesis.degree.namePh. D. in Chemistryen
thesis.degree.levelDoctorialen
dc.contributor.committeeMemberAnthony, R. G.
dc.contributor.committeeMemberKaye, H.
dc.contributor.committeeMemberPasika, Wallace M.
dc.contributor.committeeMemberWebb, L. D.
dc.type.genredissertationsen
dc.type.materialtexten
dc.format.digitalOriginreformatted digitalen
dc.publisher.digitalTexas A&M University. Libraries
dc.identifier.oclc5762690


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