Use este identificador para citar ou linkar para este item: https://repositorio.ufba.br/handle/ri/13581
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dc.contributor.authorSimplício, Lílian M. T.-
dc.contributor.authorRocha, Zênis N. da-
dc.contributor.authorGil, Marcelo P.-
dc.contributor.authorSantos, João Henrique Zimnoch dos-
dc.contributor.authorCasagrande Junior, O. L.-
dc.creatorSimplício, Lílian M. T.-
dc.creatorRocha, Zênis N. da-
dc.creatorGil, Marcelo P.-
dc.creatorSantos, João Henrique Zimnoch dos-
dc.creatorCasagrande Junior, O. L.-
dc.date.accessioned2013-11-07T11:21:02Z-
dc.date.issued2005-
dc.identifier.issn1381-1169-
dc.identifier.urihttp://repositorio.ufba.br/ri/handle/ri/13581-
dc.descriptionTexto completo: acesso restrito.p.96–101pt_BR
dc.description.abstractThe ethylene polymerization using TpMs*TiCl3 (1) (TpMs* = HB(3-mesitylpyrazolyl)2(5-mesitylpyrazolyl)−) and TpMsTiCl3 (2) (TpMs = HB(3-mesityl-pyrazolyl)3−) was performed in toluene or hexane at 60 °C in the presence of MAO or TiBA/MAO (1:1) as cocatalysts. Higher activities were found for the polymerization reactions carried out in hexane, and using a combination of TiBA/MAO as cocatalysts. Absorciometric measurements in the UV–vis region and cyclic voltammetric have shown that such complexes when activated by MAO were not stable. Measurements carried out in the presence 1-hexene have demonstrated the necessity to add the cocatalyst in the presence of an olefin, i.e., ethylene or hexene-1 in order to stabilize the active species. Furthermore, these studies have revealed that after the activation process most of Ti remains as TiIV.pt_BR
dc.language.isoenpt_BR
dc.rightsAcesso Abertopt_BR
dc.sourcehttp://dx.doi.org.ez10.periodicos.capes.gov.br/10.1016/j.molcata.2005.04.043pt_BR
dc.subjectTitaniumpt_BR
dc.subjectTris(pyrazolyl)boratept_BR
dc.subjectPolymerizationpt_BR
dc.subjectNon-metallocene catalystpt_BR
dc.titleSpectroscopic and voltametric studies in titanium tris(pyrazolyl)borate catalystspt_BR
dc.title.alternativeJournal of Molecular Catalysis A: Chemicalpt_BR
dc.typeArtigo de Periódicopt_BR
dc.identifier.numberv.238 n. 1-2pt_BR
dc.embargo.liftdate10000-01-01-
Aparece nas coleções:Artigo Publicado em Periódico (Química)

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