Abstract
The catalytic activity of nickel complexes in hydrophosphination involving secondary phosphines is not a commonly studied transformation. Beyond a small number of stand-out examples, many reports in the literature focus on the use of simple nickel salts. β-Diketiminates have been proven to be incredibly effective ligands for catalysis using a range of metal centers. This synthetic study investigates the catalytic ability of a Ni(II) β-diketiminate complex in the hydrophosphination of alkenes and alkynes, with a serendipitous discovery of its ability to effect alkyne cyclotrimerization and phosphine dehydrocoupling.
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CITATION STYLE
Webster, R. L. (2018). Room temperature Ni(II) catalyzed hydrophosphination and cyclotrimerization of alkynes. Inorganics, 6(4). https://doi.org/10.3390/inorganics6040120
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