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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/39233
Title: 
Highly selective nickel ethylene oligomerization catalysts based on sterically hindered tris(pyrazolyl)borate ligands
Author(s): 
Institution: 
  • Universidade Estadual Paulista (UNESP)
  • Universidade Federal do Rio Grande do Sul (UFRGS)
  • Univ Minnesota
ISSN: 
0276-7333
Abstract: 
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.
Issue Date: 
10-Nov-2003
Citation: 
Organometallics. Washington: Amer Chemical Soc, v. 22, n. 23, p. 4739-4743, 2003.
Time Duration: 
4739-4743
Publisher: 
Amer Chemical Soc
Source: 
http://dx.doi.org/10.1021/om034035u
URI: 
Access Rights: 
Acesso restrito
Type: 
outro
Source:
http://repositorio.unesp.br/handle/11449/39233
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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