Iminobisphosphines to (non-)symmetrical diphosphinoamine ligands: Metal-induced synthesis of diphosphorus nickel complexes and application in ethylene oligomerisation reactions
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Publication date
2014-01-01
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Abstract
We describe the synthesis of a range of novel iminobisphosphine ligands based on a sulfonamido moiety [R1SO2N=P(R 2)2-P(R3)2]. These molecules rearrange in the presence of nickel by metal-induced breakage of the P-P bond to yield symmetrical and nonsymmetrical diphosphinoamine nickel complexes of general formula Ni{[P(R2)2]N(SO2R 1)P(R3)2}Br2. The complexes can be isolated and are very stable. Upon activation by MAO, these complexes oligomerise ethylene to small chain oligomers (mainly C4-C 8) with high productivity. Surprisingly fast codimerisation reactions of ethylene with butenes is observed, leading to a high content of branched C6 products.
Keywords
Chelates, Homogeneous catalysis, Nickel, Oligomerisation, Phosphorus, Inorganic Chemistry
Citation
Boulens, P, Lutz, M, Jeanneau, E, Olivier-Bourbigou, H, Reek, J N H & Breuil, P A R 2014, 'Iminobisphosphines to (non-)symmetrical diphosphinoamine ligands : Metal-induced synthesis of diphosphorus nickel complexes and application in ethylene oligomerisation reactions', European Journal of Inorganic Chemistry, no. 23, pp. 3754-3762. https://doi.org/10.1002/ejic.201402430