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dc.contributor.authorKhamphee Phomphraien_US
dc.contributor.authorAndrew E. Fenwicken_US
dc.contributor.authorShalini Sharmaen_US
dc.contributor.authorPhillip E. Fanwicken_US
dc.contributor.authorJames M. Caruthersen_US
dc.contributor.authorW. Nicholas Delgassen_US
dc.contributor.authorMahdi M. Abu-Omaren_US
dc.contributor.authorIan P. Rothwellen_US
dc.contributor.otherPurdue University College of Scienceen_US
dc.contributor.otherPurdue Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.identifier.citationOrganometallics. Vol.25, No.1 (2006), 214-220en_US
dc.description.abstractA series of half-sandwich aryloxide titanium complexes, [CpTi(OAr)Me2] (Cp = C5H5; OAr = OC6H3Me2-2,6, OC6H3Et2-2,6, OC6H3iPr2-2,6, OC6H3tBu2-2,6, and OC6HPh4-2,3,5,6), have been synthesized. These compounds react with B(C6F5)3to give thermally unstable complexes [CpTi(OAr)Me][MeB(C6F5)3]. Two different deactivation pathways have been identified within the series. The tetraphenylphenoxide cationic methyl compound decomposes cleanly at room temperature to give [CpTi(OC6HPh4-2,3,5,6)(C6F5){CH2B(C6F5)2}] and methane with a first-order rate constant of 7.6(2) × 10-4s-1at 25°C. For relatively smaller aryloxide ligands, OAr = OC6H3iPr2-2,6, OC6H3tBu2-2,6, a Me/C6F5exchange takes place, yielding CpTi(OAr)Me(C6F5) and MeB(C6F5)2. The cationic titanium complexes are shown to be active for the polymerization of 1-hexene. At -20 and 0°C, first-order dependence on the concentration of 1-hexene is observed. The rate of polymerization decreases with increasing steric hindrance of aryloxides except for OAr = OC6HPh4-2,3,5,6. © 2006 American Chemical Society.en_US
dc.rightsMahidol Universityen_US
dc.titleDiverse pathways of activation and deactivation of half-sandwich aryloxide titanium polymerization catalystsen_US
Appears in Collections:Scopus 2006-2010

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