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Bimetallic Coordination Insertion Polymerization of Unprotected Polar Monomers: Copolymerization of Amino Olefins and Ethylene by Dinickel Bisphenoxyiminato Catalysts
Journal of the American Chemical Society (2013)
  • Madalyn R. Radlauer, California Institute of Technology
  • Aya K. Buckley, California Institute of Technology
  • Lawrence M. Henling, California Institute of Technology
  • Theodor Agapie, California Institute of Technology
Abstract
Dinickel bisphenoxyiminato complexes based on highly substituted p- and m-terphenyl backbones were synthesized, and the corresponding atropisomers were isolated. In the presence of a phosphine scavenger, Ni(COD)2, the phosphine-ligated syn-dinickel complexes copolymerized α-olefins and ethylene in the presence of amines to afford 0.2–1.3% α-olefin incorporation and copolymerized amino olefins and ethylene with a similar range of incorporation (0.1–0.8%). The present rigid catalysts provide a bimetallic strategy for insertion polymerization of polar monomers without masking of the heteroatom group. The effects of the catalyst structure on the reactivity were studied by comparisons of the syn and anti atropisomers and the p- and m-terphenyl systems.
Disciplines
Publication Date
2013
DOI
10.1021/ja4004816
Publisher Statement
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Citation Information
Madalyn R. Radlauer, Aya K. Buckley, Lawrence M. Henling and Theodor Agapie. "Bimetallic Coordination Insertion Polymerization of Unprotected Polar Monomers: Copolymerization of Amino Olefins and Ethylene by Dinickel Bisphenoxyiminato Catalysts" Journal of the American Chemical Society Vol. 135 Iss. 10 (2013) p. 3784 - 3787 ISSN: 0002-7863
Available at: http://works.bepress.com/madalyn-radlauer/8/