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Highly selective nickel ethylene oligomerization catalysts based on sterically hindered tris(pyrazolyl)borate ligands

dc.contributor.authorKunrath, F. A.
dc.contributor.authorde Souza, R. F.
dc.contributor.authorCasagrande, O. L.
dc.contributor.authorBrooks, N. R.
dc.contributor.authorYoung, V. G.
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Federal do Rio Grande do Sul (UFRGS)
dc.contributor.institutionUniv Minnesota
dc.date.accessioned2014-05-20T15:29:43Z
dc.date.available2014-05-20T15:29:43Z
dc.date.issued2003-11-10
dc.description.abstractThe reaction of TlTp' (Tp' = HB(3-mesitylpyrazolyl)(3)(-) (Tp(Ms)), HB(3-mesitylpyrazolyl)(2)(5-mesitylpyrazolyl)(-) (Tp(Ms)*)) with NiCl(2).6H(2)O affords Tp(Ms)NiCl (1) and Tp(Ms)*NiCl (2) in good yield. The compound 2 undergoes an isomerization process to form [{Tp(Ms)**}NiCl](2) (3) (Tp(Ms)** = HB(5-mesitylpyrazolyl)(2)(3-mesitylpyrazolyl)(-)) in 68% yield. Treatment of the tris(pyrazolyl)-borate nickel compounds 1 and 2 with alkylaluminum cocatalysts such as methylalumoxane (MAO) and trimethylaluminum (TMA) in toluene generates active catalysts for ethylene oligomerization. The compound 1 shows turnover frequencies in the range of (2.2-43.1) x 10(3) h(-1). Oligomerization reaction conditions can be adjusted that lead to selectivities as high as 81% for butene-1.en
dc.description.affiliationUniv Estadual Paulista, Inst Quim Araraquara, BR-14800900 Araraquara, SP, Brazil
dc.description.affiliationUniv Fed Rio Grande do Sul, Inst Quim, Lab Catalise Mol, BR-90501970 Porto Alegre, RS, Brazil
dc.description.affiliationUniv Minnesota, Dept Chem, Xray Crystallog Lab, Minneapolis, MN 55455 USA
dc.description.affiliationUnespUniv Estadual Paulista, Inst Quim Araraquara, BR-14800900 Araraquara, SP, Brazil
dc.format.extent4739-4743
dc.identifierhttp://dx.doi.org/10.1021/om034035u
dc.identifier.citationOrganometallics. Washington: Amer Chemical Soc, v. 22, n. 23, p. 4739-4743, 2003.
dc.identifier.doi10.1021/om034035u
dc.identifier.issn0276-7333
dc.identifier.urihttp://hdl.handle.net/11449/39233
dc.identifier.wosWOS:000186401300021
dc.language.isoeng
dc.publisherAmer Chemical Soc
dc.relation.ispartofOrganometallics
dc.relation.ispartofjcr4.051
dc.relation.ispartofsjr1,652
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.titleHighly selective nickel ethylene oligomerization catalysts based on sterically hindered tris(pyrazolyl)borate ligandsen
dc.typeArtigopt
dcterms.licensehttp://pubs.acs.org/paragonplus/copyright/jpa_form_a.pdf
dcterms.rightsHolderAmer Chemical Soc
dspace.entity.typePublication
unesp.author.orcid0000-0002-9855-6159[3]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt

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