Synthesis of Well-Defined Active Sites in Supported Catalysts Via An Organometallic Approach

Tuesday, November 10, 2009: 12:30 PM
Hermitage E (Gaylord Opryland Hotel)

Susannah L. Scott, Departments of Chemical Engineering and Chemistry, University of California, Santa Barbara, Santa Barbara, CA
Ying-Jen Wang Lee, Department of Chemistry, University of California, Santa Barbara, Santa Barbara, CA

This paper will discuss the synthesis of well-defined active sites in supported olefin polymerization catalysts using an organometallic approach. The reaction of B(C6F5)3 with the terminal hydroxyl groups of the silica surface proceeds via water-catalyzed displacement of C6F5H and the formation of supported Lewis acid sites, SiOB(C6F5)2. The resulting solid cocatalyst can be used to activate single-site polymerization catalysts, including Cr(CH2C(CH3)3)4. The design of active sites arises from the predictable nature of the organometallic-surface reactions, which can be demonstrated by a combination of spectroscopic and kinetic probes.
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See more of this Session: Rational Catalyst Design II
See more of this Group/Topical: Catalysis and Reaction Engineering Division