Computational Assessment of Counterion Effect of Borate Anions on Ethylene Polymerization by Zirconocene and Hafnocene Catalysts
Riffat Parveen, Thomas R. Cundari, Jarod M. Younker, George Rodríguez
Abstract
The olefin polymerization performance of metallocene catalysts strongly depends on the nature of the counteranion provided by the activator system. The relative effect of two borate anions [B(C6F5)4]− and [B(C10F7)4]− (DP– and DN–, respectively) have been quantified through computational studies. The free energies for model initiation, propagation, and termination steps of ethylene polymerization catalyzed by (SBI)MCl2 for M = Zr and Hf have been calculated, (SBI = Me2Si(1-Ind)2). Initially, the cationic catalyst active species forms an inner-sphere ion pair [SBIMMe]+[DP/N]− with M---F bonding that is weak enough to be displaced by either incoming monomer or a β-C–H agostic interaction from the growing polymer chain. Calculations indicate that formation of an ion-pair complex is highly exergonic in all cases (ca. −25 kcal/mol). Formation of a monomer π-complex where ethylene is bonded to the inner coordination sphere of M is always downhill with reference to the corresponding outer-sphere isomers. Similarly, formation of the transition states for monomer insertion (TS1 and TS2) is higher for DP– versus DN–. These differences shed light on the observed performance of metallocene catalysts as a function of changing the counterion used.