The homopolymerization of ethylene by using different catalytic systems based on dinitro-substituted bis(salicylaldiminate)nickel(II) precursors such as bis[3,5dinitro-N(2,6-diisopropylphenyl)]nickel(II) and bis[3,5-dinitro-N(phenyl)]nickel(II) in combination with organoaluminum compounds was investigated. In particular, the catalytic performances were studied as a function of the main reaction parameters, such as temperature, pressure, Al/Ni molar ratio, and duration. Methylaluminoxane resulted in the best co-catalyst. Activities up to 200 kg polyethylene/(mol Ni X h) to give a linear high-molecular-weight polymer were achieved. The influence of the bulkiness of the substituents on the N-aryl group of the aldimine ligand was also checked; it resulted in a determinant for catalytic activity rather than for polymer characteristics. (C) 2004 Wiley Periodicals, Inc.

Ethylene polymerization by bis(salicylaldiminate)nickel(II)/Aluminoxane catalysts

CARLINI, CARLO;RASPOLLI GALLETTI, ANNA MARIA;SBRANA, GLAUCO;
2004-01-01

Abstract

The homopolymerization of ethylene by using different catalytic systems based on dinitro-substituted bis(salicylaldiminate)nickel(II) precursors such as bis[3,5dinitro-N(2,6-diisopropylphenyl)]nickel(II) and bis[3,5-dinitro-N(phenyl)]nickel(II) in combination with organoaluminum compounds was investigated. In particular, the catalytic performances were studied as a function of the main reaction parameters, such as temperature, pressure, Al/Ni molar ratio, and duration. Methylaluminoxane resulted in the best co-catalyst. Activities up to 200 kg polyethylene/(mol Ni X h) to give a linear high-molecular-weight polymer were achieved. The influence of the bulkiness of the substituents on the N-aryl group of the aldimine ligand was also checked; it resulted in a determinant for catalytic activity rather than for polymer characteristics. (C) 2004 Wiley Periodicals, Inc.
2004
Carlini, Carlo; A., Macinai; F., Masi; RASPOLLI GALLETTI, ANNA MARIA; R., Santi; Sbrana, Glauco; A., Sommazzi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/184043
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