Ring-opening polymerization of 1-phenyl-20vinylcyclopropane derivatives by ziegler-natta catalysts지글러-나타 촉매에 의한 1-페닐-2-비닐시클로프로판 유도체의 개환중합

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dc.contributor.advisorCho, I-Whan-
dc.contributor.advisor조의환-
dc.contributor.authorSong, Soo-Suk-
dc.contributor.author송수석-
dc.date.accessioned2011-12-13T04:25:07Z-
dc.date.available2011-12-13T04:25:07Z-
dc.date.issued1989-
dc.identifier.urihttp://library.kaist.ac.kr/search/detail/view.do?bibCtrlNo=61252&flag=dissertation-
dc.identifier.urihttp://hdl.handle.net/10203/31309-
dc.description학위논문(박사) - 한국과학기술원 : 화학과, 1989.2, [ viii, 99 p. ]-
dc.description.abstractp-Substtituted phenylvinylcyclopropanes, 1-phenyl-2-vinyl-cyclopropane, 1-(p-anisyl)-2-vinylcyclopropane, 1-(p-tolyl)-2-vinylcyclopropane, 1-(p-chlorophenyl)-2-vinyl-cyclopropane and 1-(p-cyanophenyl)-2-vinylcyclopropane, were synthesized and polymerized with various initiators such as Ziegler-Natta catalysts. Their polymerization behavior, characterization and the properties of the resulting polymers were also investigated. Those five p-substituted phenylvinylcyclopropanes exhibited quite different polymerization behavior depending on the properties of their substituents. Polymerization results showed that the monomers with electron-donating substituents were readily polymerizable with Ziegler-Natta catalysts and cationic initiators, whereas the monomers with electron-withdrawing groups were not. And the opposite trend was observed in the polymerization with radical initiators. In the polymerization of methoxy- and methyl-substituted monomers, acidic organoaluminum compounds such as $AlEtCl_2$ based on metal halides were very effective cocatalysts. Ziegler-Natta polymerization is considered to proceed through the proposed coordination mechanism in which a monomer molecule is first coordinated at the catalyst site before propagation and the propagating species then attacks the activated benzylic carbon position of the coordinated monomer to yield 1,5-addition polymers. In radical polymerization of chloro- and cyano-substituted monomers, the reaction is considered to proceed through a mechanism in that a radical attacks at first on the vinyl group to form a cyclopropylcarbinyl radical and then this radical isomerizes to an allylcarbinyl radical with ring-opening. Allylcarbinyl radical will then react with another monomer to propagate. The polymers produced were confirmed to have the structures of five carbon-repeating unit and the double bonds in the polymer chain were in trans form. All the polymers were soluble in common solvents and flexible film-forming mate...eng
dc.languageeng-
dc.publisher한국과학기술원-
dc.titleRing-opening polymerization of 1-phenyl-20vinylcyclopropane derivatives by ziegler-natta catalysts-
dc.title.alternative지글러-나타 촉매에 의한 1-페닐-2-비닐시클로프로판 유도체의 개환중합-
dc.typeThesis(Ph.D)-
dc.identifier.CNRN61252/325007-
dc.description.department한국과학기술원 : 화학과, -
dc.identifier.uid000835934-
dc.contributor.localauthorCho, I-Whan-
dc.contributor.localauthor조의환-
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