Catalyst Nuclearity Effects on Stereo- and Regioinduction in Pyridylamidohafnium-Catalyzed Propylene and 1-Octene Polymerizations

Abstract

In comparison to monometallic controls, bimetallic olefin polymerization catalysts often exhibit superior performance in terms of higher polyolefin Mw, higher comonomer incorporation, and higher polar comonomer tolerance. However, using cooperating catalyst centers to modulate stereoselectivity in α-olefin polymerizations is relatively unexplored. In this contribution, the monometallic Hf(IV) complex, L1-HfMe2 (catalyst A, L1 = 2,6-diisopropyl-N-{(2-isopropylphenyl)[6-(naphthalen-1-yl)pyridin-2-yl]methyl}aniline), and homo-bimetallic Hf(IV) complexes, L2-Hf2Me5 (catalyst B) and L2-Hf2Me4 (catalyst C) (L2 = N,N′-{[naphthalene-1,4-diylbis(pyridine-6,2-diyl)]bis[(2-isopropylphenyl)methylene)]bis(2,6-diisopropylaniline}), are activated with Ph3C+B(C6F5)4– and investigated in propylene and 1-octene homopolymerizations. In propylene polymerizations, the conformationally flexible catalyst B-derived bimetallic dicationic catalyst produces higher Mw polypropylene (up to 7.8×), higher total stereo- and regiodefect densities (up to 3.5×), and lower Tm (by as much as ∼14 °C) versus the monometallic catalyst A-derived control. In 1-octene polymerizations, the conformationally flexible catalyst B-derived bimetallic dicationic catalyst induces greatly reduced isotacticity (23% reduction in [mmmm]) versus the catalyst A-derived monometallic control ([mmmm] > 99%). Interestingly, conformationally flexible catalyst B-derived cationic bimetallic Hf catalysts are also known to undergo rapid intramolecular/intermetal methyl exchange and to exhibit strong Hf···Hf cooperative enchainment effects in ethylene homo- and copolymerizations. Steric effects and intramolecular intermetal chain transfer likely both contribute to the increased isotactic polyolefin stereo- and regiodefect content.