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Kinetic Studies of the Copolymerization of Ethylene and Norbornene by ansa Zirconocene/Methylaluminoxane Catalysts: Evidence of a Long Lasting -....... (Articolo in rivista)

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Kinetic Studies of the Copolymerization of Ethylene and Norbornene by ansa Zirconocene/Methylaluminoxane Catalysts: Evidence of a Long Lasting -....... (Articolo in rivista) (literal)

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Jansen J.C. , Mendichi R. , Sacchi M.C. , Tritto I. (2003)
Kinetic Studies of the Copolymerization of Ethylene and Norbornene by ansa Zirconocene/Methylaluminoxane Catalysts: Evidence of a Long Lasting -.......
in Macromolecular chemistry and physics (Print); Wiley-VCH - Weinheim, Wheinheim (Germania)
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Istituto di Chimica delle Macromolecole del CNR, Via E. Bassini 15, I-20133 Milano, Italy (literal)

Titolo

Kinetic Studies of the Copolymerization of Ethylene and Norbornene by ansa Zirconocene/Methylaluminoxane Catalysts: Evidence of a Long Lasting -....... (literal)

Abstract

Copolymers of ethylene (E) with norbornene (N) were synthesized using the catalysts rac-Et(Ind)2ZrCl2/ MAO (1), 90%rac/10%meso-Et(4,7-Me2Ind)2ZrCl2/MAO (2), and rac-H2C(3-t-BuInd)2ZrCl2/MAO (3). Catalyst activity, molar mass (MM), and copolymer composition were studied as a function of time. The polymers showed an unusually narrow molar mass distribution (MMD) and a significant increase of their MM with time for up to one hour, suggesting a quasi-living polymerization at 30 °C. The experimental data were fitted to kinetic equations and the propagation and transfer reactions were described in quantitative terms. Norbornene greatly depressed the propagation rate, along with the chain transfer rate. The more sterically hindered catalysts of the series showed lower propagation and chain transfer turnover frequency than 1 and yielded polymers with a low (2) to very low (3) norbornene content. The presence of norbornene in solution seemed to be one of the main factors responsible for the observed quasi living character of the copolymerization, probably due to coordination of norbornene to the active site. Time-resolved kinetic studies also allowed for the calculation of the fraction of active metal centers, ranging from 56% (3) and 6668% (1) to 94% (2) of the total zirconium present, depending on catalyst structure. (literal)

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