Constrained ligand architectures in late transition metal bisimine polymerization catalysts

INOR 273

Dennis Leung, dleung@uci.edu, Xuebin Shao, and Zhibin Guan, zguan@uci.edu. Department of Chemistry, University of California, Irvine, 1123 Reines Hall, UC Irvine, Irvine, CA 92697
Our group has recently reported the development of cyclophane-based bisimine ligand scaffolds capable of complexing nickel and palladium polymerization catalysts. These catalysts have greatly increased thermal stability as well as novel branching selectivities in the polymerization of olefins compared to traditional Brookhart-type bisimine catalysts. Our current research is focused on the development of novel sterically constrained bisimine ligands for thermally robust polyemerization catalysts. Our results have shown that a tigher, more sterically congested environment increases the stability of the catalyst, especially at high temperatures. By varying the active site cavity of the embedded metal center, the stability, reactivity, and selectivity of the polymerization catalysts can be tuned.
 

Organometallic Catalysts
7:00 PM-10:00 PM, Sunday, August 19, 2007 BCEC -- Exhibit Hall - B2, Poster

Sci-Mix
8:00 PM-10:00 PM, Monday, August 20, 2007 BCEC -- Exhibit Hall - B2, Sci-Mix

Division of Inorganic Chemistry

The 234th ACS National Meeting, Boston, MA, August 19-23, 2007