Abstract

The cyclodimer distribution in the Ni0/PR3-catalyzed oligomerization of butadiene depends upon “electronic” factors of the ligands. An opposing effect must also be considered, viz. a ligand-induced relative activation or inhibition of the product-forming reaction step. (VCH = vinylcyclohexane, COD = 1,5-cyclooctadiene, Su = substrate = butadiene, m = 0 or 1.)

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