Organometallics, volume 36, issue 12, pages 2338-2344
Side-Arm Control in Phosphine-Sulfonate Palladium- and Nickel-Catalyzed Ethylene Polymerization and Copolymerization
Tao Liang
1
,
Changle Chen
1
Publication type: Journal Article
Publication date: 2017-06-15
Journal:
Organometallics
scimago Q1
SJR: 0.654
CiteScore: 5.6
Impact factor: 2.5
ISSN: 02767333, 15206041
Organic Chemistry
Inorganic Chemistry
Physical and Theoretical Chemistry
Abstract
A series of phosphine-sulfonate ligands bearing various side-arm substituents were designed and prepared. The corresponding Pd(II) complexes [κ2-(P,O)-2-(PPhAr)-1-benzenesulfonato]Pd(Me)(dmso) (Pd1, Ar = o-MeO-C6H4; Pd2, Ar = o-PhO-C6H4; Pd3, Ar = o-(2,6-Me2-C6H3)O-C6H4; Pd4, Ar = o-PhSO2-C6H4) and Ni(II) complexes [κ2-(P,O)-2-(PPhAr)-1-benzenesulfonato]NiPh(PPh3) (Ni1, Ar = o-MeO-C6H4; Ni2, Ar = o-PhO-C6H4; Ni3, Ar = o-(2,6-Me2-C6H3)O-C6H4; Ni4, Ar = o-PhSO2-C6H4) were prepared and applied in ethylene polymerization and ethylene–polar monomer copolymerization. Catalysts Pd2, Pd3, Ni2, and Ni3 are moderately active in ethylene polymerization (activity up to 8.7 × 105 g mol–1 h–1), generating polyethylene with high molecular weights (Mn up to 105100) and high melting temperatures (Tm up to 131.6 °C). The two palladium catalysts can also initiate efficient copolymerization of ethylene with methyl acrylate, allyl cyanide, and allyl acetate. Most importantly, high copolymer molecular weights (Mn between 21600...
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