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Bimetallic effects on ethylene polymerization in the presence of amines: inhibition of the deactivation by Lewis bases.


ABSTRACT: Dinickel complexes supported by terphenyl ligands appended with phenoxy and imine donors were synthesized. Full substitution of the central arene blocks rotation around the aryl-aryl bond and allows for the isolation of atropisomers. The reported complexes perform ethylene polymerization in the presence of amines. The inhibiting effect of polar additives is up to 250 times lower for the syn isomer than the anti isomer. Comparisons with mononuclear systems indicate that the proximity of the metal centers leads to the observed inhibitory effect on the deactivation of the catalysts.

SUBMITTER: Radlauer MR 

PROVIDER: S-EPMC3307529 | biostudies-literature | 2012 Jan

REPOSITORIES: biostudies-literature

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Bimetallic effects on ethylene polymerization in the presence of amines: inhibition of the deactivation by Lewis bases.

Radlauer Madalyn R MR   Day Michael W MW   Agapie Theodor T  

Journal of the American Chemical Society 20120112 3


Dinickel complexes supported by terphenyl ligands appended with phenoxy and imine donors were synthesized. Full substitution of the central arene blocks rotation around the aryl-aryl bond and allows for the isolation of atropisomers. The reported complexes perform ethylene polymerization in the presence of amines. The inhibiting effect of polar additives is up to 250 times lower for the syn isomer than the anti isomer. Comparisons with mononuclear systems indicate that the proximity of the metal  ...[more]

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