Issue 5, 2003

Synthetic, spectroscopic and olefin oligomerisation studies on nickel and palladium complexes containing ferrocene substituted nitrogen donor ligands

Abstract

A series of new pyridyl- and quinolyl-N-substituted ferrocenyl and ferrocenediyl ligands have been conveniently synthesised and characterised and their coordination chemistry probed by reaction with a range of nickel and palladium reagents. The bidentate, chelating nature of each arm is demonstrated, especially using X-ray crystallography, though subtle changes in the steric bulk around the ligand enforces other bonding modes. Electrochemical studies show the expected shift of the FeII/FeIII redox couple on coordination of the metal centre(s) to the ligands, and polymerisation studies indicate that the nickel-based complexes act as very efficient pre-catalysts for the formation of short chain oligomers.

Graphical abstract: Synthetic, spectroscopic and olefin oligomerisation studies on nickel and palladium complexes containing ferrocene substituted nitrogen donor ligands

Supplementary files

Article information

Article type
Paper
Submitted
24 Oct 2002
Accepted
03 Jan 2003
First published
30 Jan 2003

Dalton Trans., 2003, 918-926

Synthetic, spectroscopic and olefin oligomerisation studies on nickel and palladium complexes containing ferrocene substituted nitrogen donor ligands

V. C. Gibson, C. M. Halliwell, N. J. Long, P. J. Oxford, A. M. Smith, A. J. P. White and D. J. Williams, Dalton Trans., 2003, 918 DOI: 10.1039/B210463F

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