1996Macromolecular Chemistry and PhysicsRequires access

Copolymerization of ethylene and styrene with monocyclopentadienyltitanium trichloride/methylalumoxane catalyst

Leone Oliva, Stefano Mazza, Pasquale Longo

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Abstract

Abstract A series of ethylene‐styrene copolymerizations was carried out in the presence of cyclopentadienyltitanium trichloride and methylalumoxane at 20°C and at different comonomer feed compositions. By sequential extraction a copolymeric material with a styrene units content up to 36 mol‐% can be separated from the homopolymeric products. Some considerations about the relative reactivity of the comonomers and the regioregularity of the styrene insertion are made on the basis of the 13C NMR spectra.

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Abstract A series of ethylene‐styrene copolymerizations was carried out in the presence of cyclopentadienyltitanium trichloride and methylalumoxane at 20°C and at different comonomer feed compositions. By sequential extraction a copolymeric material with a styrene units content up to 36 mol‐% can be separated from the homopolymeric products. Some considerations about the relative reactivity of the comonomers and the regioregularity of the styrene insertion are made on the basis of the 13C NMR spectra.

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Available abstract

Abstract A series of ethylene‐styrene copolymerizations was carried out in the presence of cyclopentadienyltitanium trichloride and methylalumoxane at 20°C and at different comonomer feed compositions. By sequential extraction a copolymeric material with a styrene units content up to 36 mol‐% can be separated from the homopolymeric products. Some considerations about the relative reactivity of the comonomers and the regioregularity of the styrene insertion are made on the basis of the 13C NMR spectra.

Key concepts: Comonomer, Styrene, Copolymer, Ethylene, Polymer chemistry, Reactivity (psychology), Chemistry, Catalysis

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