Hafnium Bis(phenoxyimino) Dibenzyl Complexes and Their Activation toward Olefin Polymerization

Hf bis(phenoxyimino) dibenzyl complexes bearing benzylimino and perfluorophenylimino groups were prepared by a direct reaction between the desired ligand precursors and Hf(CH2Ph)4. In the solid state, the Hf complexes adopt an octahedral configuration where imino nitrogens are in positions cis to ea...

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Bibliographic Details
Published in:Organometallics Vol. 26; no. 6; pp. 1444 - 1460
Main Authors: Axenov, Kirill V, Klinga, Martti, Lehtonen, Olli, Koskela, Harri T, Leskelä, Markku, Repo, Timo
Format: Journal Article
Language:English
Published: American Chemical Society 12-03-2007
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Summary:Hf bis(phenoxyimino) dibenzyl complexes bearing benzylimino and perfluorophenylimino groups were prepared by a direct reaction between the desired ligand precursors and Hf(CH2Ph)4. In the solid state, the Hf complexes adopt an octahedral configuration where imino nitrogens are in positions cis to each other and oxygens occupy apical vertices of the coordination polyhedron. According to 1H NMR and 2D-NOESY studies, this cis-N,N configuration was also maintained in solution. In addition, the structures of Hf bis(phenoxyimino) dibenzyl complexes were studied with DFT calculations. Activation of the Hf dibenzyl complexes with B(C6F5)3 led to the highly air-, moisture-, solvent-, and temperature-sensitive cationic bis(phenoxyimino) Hf monobenzyl species, which were further investigated by 1H and 19F NMR, 1H−13C heteronuclear correlation, 2D-NOESY, and ESI-MS methods. It was observed that the cationic, benzylimino-substituted Hf complexes have a propensity toward CH activation. The correlation between the stability of the cationic species toward CH activation and the catalytic behavior of the MAO-activated dibenzyl complexes was established. Accordingly, the MAO-activated Hf bis(phenoxyimino) dibenzyl complexes and their dichloro analogues, depending on the ligand substitution, have from low to very high catalytic activities (up to 14 000 kg of PE/((mol of cat.) h (bar of ethylene))) in ethylene polymerizations. In general, the produced polyethylene had a monomodal molar mass distribution with relatively narrow polydispersity. Polypropylene produced with perfluorophenyl-substituted Hf complexes had a large amount of 2,1-misinsertions in the polymer chains. To further shed light on the catalytic reaction, polymerizations of ethylene and propylene with the cationic species generated from Hf bis(phenoxyimino) dibenzyl complexes with B(C6F5)3 were studied with 1H NMR.
Bibliography:ark:/67375/TPS-H868XL9G-3
istex:455B227FE07E6F40DF5DC65632838A728EE10F92
ISSN:0276-7333
1520-6041
DOI:10.1021/om060753f