Abstract
Treatment of the five-coordinate ferrous dialkyl complex, (iPrPDI)Fe(CH2SiMe3)2 (iPrPDI = ((2,6-CHMe2)2C6H3N=CMe)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.
Original language | English (US) |
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Pages (from-to) | 9660-9661 |
Number of pages | 2 |
Journal | Journal of the American Chemical Society |
Volume | 127 |
Issue number | 27 |
DOIs | |
State | Published - Jul 13 2005 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- General Chemistry
- Biochemistry
- Catalysis
- Colloid and Surface Chemistry