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http://acervodigital.unesp.br/handle/11449/39233
- Title:
- Highly selective nickel ethylene oligomerization catalysts based on sterically hindered tris(pyrazolyl)borate ligands
- Universidade Estadual Paulista (UNESP)
- Universidade Federal do Rio Grande do Sul (UFRGS)
- Univ Minnesota
- 0276-7333
- The 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.
- 10-Nov-2003
- Organometallics. Washington: Amer Chemical Soc, v. 22, n. 23, p. 4739-4743, 2003.
- 4739-4743
- Amer Chemical Soc
- http://dx.doi.org/10.1021/om034035u
- Acesso restrito
- outro
- http://repositorio.unesp.br/handle/11449/39233
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