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Use este identificador para citar ou linkar para este item: https://repositorio.ufba.br/handle/ri/14904
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dc.contributor.authorGheno, Grasiela-
dc.contributor.authorBasso, Nara Regina de Souza-
dc.contributor.authorCeschi, Marco Antônio-
dc.contributor.authorLivotto, Paolo R.-
dc.contributor.authorNascimento, Alanjone Azevedo-
dc.contributor.authorRocha, Zênis N. da-
dc.contributor.authorGalland, Griselda Barrera-
dc.creatorGheno, Grasiela-
dc.creatorBasso, Nara Regina de Souza-
dc.creatorCeschi, Marco Antônio-
dc.creatorLivotto, Paolo R.-
dc.creatorNascimento, Alanjone Azevedo-
dc.creatorRocha, Zênis N. da-
dc.creatorGalland, Griselda Barrera-
dc.date.accessioned2014-05-06T12:10:13Z-
dc.date.issued2013-
dc.identifier.issn0926-860X-
dc.identifier.urihttp://repositorio.ufba.br/ri/handle/ri/14904-
dc.descriptionTexto completo: acesso restrito. p. 439–449pt_BR
dc.description.abstractTwo new complexes of Ti and Zr were synthesized with 3-hydroxyflavone bidentate ligand and investigated in homogeneous ethylene polymerization. Both complexes were characterized by UV–VIS, 1H and 13C NMR, and electrochemical studies. The geometries and energies of all possible isomeric species were studied by full unconstrained optimizations performed at Density Functional Theory (DFT) level. The polymerization reactions were performed at different experimental conditions with methylaluminoxane (MAO), as the cocatalyst. Both complexes were active in ethylene polymerization in all the conditions used. However, zirconium complex showed the best activity comparing to the titanium complex at 2500 Al/M ratio. The polymers obtained were high density polyethylene with ultra high molecular weights.pt_BR
dc.language.isoenpt_BR
dc.rightsAcesso Abertopt_BR
dc.sourcehttp://dx.doi.org/10.1016/j.apcata.2013.08.015pt_BR
dc.subjectSynthesispt_BR
dc.subjectComplexpt_BR
dc.subject3-Hydroxyflavonept_BR
dc.subjectCatalystpt_BR
dc.subjectPolyethylenept_BR
dc.titleFlavone complexes of Ti and Zr active in ethylene polymerizationpt_BR
dc.title.alternativeApplied Catalysis A: Generalpt_BR
dc.typeArtigo de Periódicopt_BR
dc.identifier.numberv. 467pt_BR
dc.embargo.liftdate10000-01-01-
Aparece nas coleções:Artigo Publicado em Periódico (Química)

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