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Switching a Catalyst System from Ethene Polymerization to Ethene Trimerization with a Hemilabile Ancillary Ligand
Patrick J W Deckers1, Bart Hessen1, Jan H Teuben1
1Dutch Polymer Institute/Center for Catalytic Olefin Polymerization Stratingh Institute for Chemistry and Chemical Engineering University of Groningen Nijenborgh 4, 9747 AG Groningen (The Netherlands) Fax: (+31) 50-3634315.
Abstract:
A drastic ligand effect was observed in the catalytic ethene conversion by the substituted mono(cyclopentadienyl)titaniumtrichloride/methylalumoxane (MAO) catalysts shown. The catalyst with R=Me produces polyethene, whereas the catalyst with R=Ph selectively trimerizes ethene to 1-hexene. This switch in catalyst performance appears to be the result of a hemilabile behavior of the cyclopentadienyl ligand with the pendant arene group, involving reversible coordination of the arene moiety.
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