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bis(N-(3-tert-butylsalicylidene)-2,3,4,5,6-pentafluoroanilinato)hafnium dichloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

565238-05-3

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565238-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 565238-05-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,5,2,3 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 565238-05:
(8*5)+(7*6)+(6*5)+(5*2)+(4*3)+(3*8)+(2*0)+(1*5)=163
163 % 10 = 3
So 565238-05-3 is a valid CAS Registry Number.

565238-05-3Downstream Products

565238-05-3Relevant academic research and scientific papers

Hafnium bis(phenoxyimino) dibenzyl complexes and their activation toward olefin polymerization

Axenov, Kirill V.,Klinga, Martti,Lehtonen, Olli,Koskela, Harri T.,Leskelae, Markku,Repo, Timo

, p. 1444 - 1460 (2008/10/09)

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(C6F 5)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(C 6F5)3 were studied with 1H NMR.

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