Reversible chain transfer between organoyttrium cations and aluminum: synthesis of aluminum-terminated polyethylene with extremely narrow molecular-weight distribution |
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Authors: | Kretschmer Winfried P Meetsma Auke Hessen Bart Schmalz Thomas Qayyum Sadaf Kempe Rhett |
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Institution: | Stratingh Institut for Chemistry and Chemical Engineering, Center for Catalytic Olefin Polymerization, University of Groningen, Nijenborgh 4 9747 AG Groningen, The Netherlands. W.P.Kretschmer@rug.nl |
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Abstract: | Aminopyridinato-ligand-stabilized organoyttrium cations are accessible in very good yield through alkane elimination from trialkyl yttrium complexes with sterically demanding aminopyridines, followed by abstraction of one of the two alkyl functions using ammonium borates. At 80 degrees C and in the presence of small amounts of aluminum alkyl compounds, very high ethylene polymerization activities are observed if very bulky aminopyridinato ligands are used. During these polymerizations a reversible polyethylene chain transfer is observed between the organoyttrium cations and aluminum alkyls. The chain-transfer catalyst system described here is able to produce relatively long-chain (up to 4000 g mol-1) Al-terminated polyethylene with a molecular-weight distribution<1.1. In the synthesis of higher molecular PE a slight increase in polydispersity with increasing chain length (15,600 g mol-1, approximately 1.4) is observed owing to reduced reversibility caused by higher viscosity and precipitation of polymer chains (temperature of 80-100 degrees C). |
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Keywords: | aluminum chain transfer lanthanides polymerization yttrium |
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