Nature of the initiation, propagation, and chain transfer steps during the formation of ethylene oligomers catalyzed by PdMe2(N,N,N′N′-tetramethylethylenediamine)/B(C6F5)3
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Desjardins, SY
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Queens Univ, Dept Chem, Kingston, ON K7L 3N6, CanadaQueens Univ, Dept Chem, Kingston, ON K7L 3N6, Canada
Desjardins, SY
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Way, AA
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Queens Univ, Dept Chem, Kingston, ON K7L 3N6, CanadaQueens Univ, Dept Chem, Kingston, ON K7L 3N6, Canada
Way, AA
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Murray, MC
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Queens Univ, Dept Chem, Kingston, ON K7L 3N6, CanadaQueens Univ, Dept Chem, Kingston, ON K7L 3N6, Canada
Murray, MC
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Adirim, D
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Queens Univ, Dept Chem, Kingston, ON K7L 3N6, CanadaQueens Univ, Dept Chem, Kingston, ON K7L 3N6, Canada
Adirim, D
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Baird, MC
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Queens Univ, Dept Chem, Kingston, ON K7L 3N6, CanadaQueens Univ, Dept Chem, Kingston, ON K7L 3N6, Canada
Baird, MC
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]
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[1] Queens Univ, Dept Chem, Kingston, ON K7L 3N6, Canada
Reaction of equimolar quantities of PdMe2(Me2NCH2CH2NMe2) and B(C6F5)(3) in the presence of ethylene results in the formation of [PdMe(C2H4)(Me2NCH2CH2NMe2)](+)[BMe(C6F5)(3)](-); the latter catalyzes the oligomerization of ethylene to highly branched products, which are apparently formed via both reversible beta-elimination-reinsertion processes and the incorporation of short chain oligomeric products.