Formation of trivalent zirconocene complexes from ansa-zirconocene-based olefin-polymerization precatalysts: an EPR- and NMR-spectroscopic study

Taylor N Lenton; John E Bercaw; Valentina N Panchenko; Vladimir A Zakharov; Dmitrii E Babushkin; Igor E Soshnikov; Evgenii P Talsi; Hans H Brintzinger

doi:10.1021/ja403170u

Formation of trivalent zirconocene complexes from ansa-zirconocene-based olefin-polymerization precatalysts: an EPR- and NMR-spectroscopic study

J Am Chem Soc. 2013 Jul 24;135(29):10710-9. doi: 10.1021/ja403170u. Epub 2013 Jul 10.

Authors

Taylor N Lenton¹, John E Bercaw, Valentina N Panchenko, Vladimir A Zakharov, Dmitrii E Babushkin, Igor E Soshnikov, Evgenii P Talsi, Hans H Brintzinger

Affiliation

¹ Arnold and Mabel Beckman Laboratories of Chemical Synthesis, California Institute of Technology, Pasadena, California 91125, USA.

PMID: 23745750
DOI: 10.1021/ja403170u

Abstract

Reduction of Zr(IV) metallocenium cations with sodium amalgam (NaHg) produces EPR signals assignable to Zr(III) metallocene complexes. The chloro-bridged heterodinuclear ansa-zirconocenium cation [(SBI)Zr(μ-Cl)2AlMe2](+) (SBI = rac-dimethylsilylbis(1-indenyl)), present in toluene solution as its B(C6F5)4(-) salt, thus gives rise to an EPR signal assignable to the complex (SBI)Zr(III)(μ-Cl)2AlMe2, while (SBI)Zr(III)-Me and (SBI)Zr(III)(μ-H)2Al(i)Bu2 are formed by reduction of [(SBI)Zr(μ-Me)2AlMe2](+) B(C6F5)4(-) and [(SBI)Zr(μ-H)3(Al(i)Bu2)2](+) B(C6F5)4(-), respectively. These products can also be accessed, along with (SBI)Zr(III)-(i)Bu and [(SBI)Zr(III)](+) AlR4(-), when (SBI)ZrMe2 is allowed to react with HAl(i)Bu2, eliminating isobutane en route to the Zr(III) complex. Further studies concern interconversion reactions between these and other (SBI)Zr(III) complexes and reaction mechanisms involved in their formation.