Iminobisphosphines to (non-)symmetrical diphosphinoamine ligands: Metal-induced synthesis of diphosphorus nickel complexes and application in ethylene oligomerisation reactions

Pierre Boulens, Martin Lutz, Erwann Jeanneau, Hélène Olivier-Bourbigou, Joost N H Reek, Pierre Alain R Breuil

    Research output: Contribution to journalArticleAcademicpeer-review

    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.

    Original languageEnglish
    Pages (from-to)3754-3762
    Number of pages9
    JournalEuropean Journal of Inorganic Chemistry
    Issue number23
    DOIs
    Publication statusPublished - 1 Jan 2014

    Keywords

    • Chelates
    • Homogeneous catalysis
    • Nickel
    • Oligomerisation
    • Phosphorus

    Fingerprint

    Dive into the research topics of 'Iminobisphosphines to (non-)symmetrical diphosphinoamine ligands: Metal-induced synthesis of diphosphorus nickel complexes and application in ethylene oligomerisation reactions'. Together they form a unique fingerprint.

    Cite this