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dc.creatorRABAGLIATI,FRANCO M.
dc.creatorPÉREZ,MÓNICA. A.
dc.creatorCANCINO,RODRIGO A.
dc.creatorSOTO,MARCELO A.
dc.creatorRODRÍGUEZ,FRANCISCO J.
dc.creatorLEÓN,ARTURO G.
dc.creatorAYAL,HUGO A.
dc.creatorQUIJADA,RAÚL
dc.date2000-06-01
dc.date.accessioned2022-08-29T19:34:09Z
dc.date.available2022-08-29T19:34:09Z
dc.identifierhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0366-16442000000200008
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/206051
dc.descriptionCombination of diphenylzinc, Ph2Zn, cyclopentadienyl titanium trichloride, CpTiCl3, and methylaluminoxane, MAO, were used to initiate styrene, S, polymerization and its copolymerization with 1-hexadecene, 1-C16H32, and with p-tert-butylstyrene, p-ButS. For homopolymerization an almost pure syndiotatic polystyrene, s-PS, was obtained when using Ph2Zn-CpTiCl3-MAO combination, while other combinations of these components produced atactic polystyrene, a-PS, or almost no polymer at all. CpTiCl3-MAO and Ph2Zn-CpTiCl3-MAO were effective initiator systems for S/1-C16H32 and for S/p-ButS copolymerization. S/1-C16H32 copolymers showed crystalline melting temperature at range 235 - 255 °C while S/p-ButS copolymers did not show any melting temperature signal at DSC, but behave as stereoregular polymer
dc.formattext/html
dc.languageen
dc.publisherSociedad Chilena de Química
dc.relation10.4067/S0366-16442000000200008
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceBoletín de la Sociedad Chilena de Química v.45 n.2 2000
dc.subjectstyrene
dc.subjectpolymerization
dc.subjectcopolymerization
dc.subjectdiphenylzinc
dc.subjectmetallocenes
dc.subjectcatalysts
dc.subjectstereoregularity
dc.subjecttacticity
dc.titlePOLYMERIZATION OF STYRENE BY DIPHENYLZINC-ADDITIVE SYSTEMS. PART X. HOMO- AND COPOLYMERIZATION OF STYRENE USING Ph2Zn - METALLOCENE - MAO SYSTEMS


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