Bis(imino)pyridine Iron(II) Alkyl Cations for Olefin Polymerization

Marco W. Bouwkamp, Emil Lobkovsky, and Paul J. Chirik*
Department of Chemistry and Chemical Biology, Baker Laboratory, Cornell University, Ithaca, New York 14853
J. Am. Chem. Soc., 2005, 127 (27), pp 9660–9661
DOI: 10.1021/ja0524447
Publication Date (Web): June 16, 2005
Copyright © 2005 American Chemical Society
*

In papers with more than one author, the asterisk indicates the name of the author to whom inquiries about the paper should be addressed.

, pc92@cornell.edu

Abstract

Abstract Image

Treatment of the five-coordinate ferrous dialkyl complex, (iPrPDI)Fe(CH2SiMe3)2 (iPrPDI = ((2,6-CHMe2)2C6H3NCMe)2C5H3N), with [PhMe2NH][BPh4] in the presence of diethyl ether or tetrahydrofuran furnished the corresponding alkyl cations, where the donor ligand is coordinated in the basal plane of a distorted square pyramidal iron(II) alkyl cation. Performing the same reaction with the neutral Lewis acid, B(C6F5)3, induced methide abstraction from a silicon atom followed by rearrangement to afford the base free ferrous alkyl cation, [(iPrPDI)Fe(CH2SiMe2CH2SiMe3)][MeB(C6F5)3]. This complex is active for the polymerization of ethylene and yields polymers that are of higher molecular weight and narrower polydispersity than traditional methylalumoxane-activated catalysts.

Tools

History

  • Published In Issue July 13, 2005
  • Received April 14, 2005

Recommend & Share

Related Content

Other ACS content by these authors: