Issue 12, 2013

Ethylenepolymerisation and oligomerisation with arene-substituted phenoxy-imine complexes of titanium: investigation of multi-mechanism catalytic behaviour

Abstract

A range of unsubstituted (1,2) and 6-substituted (3–5) ortho-phenoxy-imine ligands have been prepared and converted to their silyl ether derivatives (6–10). Reaction of silyl ethers with TiCl4(thf)2 in the case of the unsubstituted species yields bis-ligated complexes while the substituted species react cleanly to yield complexes of the form [Ti(O^NR)Cl3(thf)]. In most cases the complexes have been characterised by X-ray crystallography. Testing of the complexes for ethylene oligomerisation and polymerisation has been undertaken employing alkylaluminium co-catalysts (AlEt3, MAO). In all cases the predominant product formed is polyethylene however careful analysis of the liquid phase reveals a complex process by which 1-butene is most likely formed via Cossee mechanism while 1-hexene results from a metallacyclic process.

Graphical abstract: Ethylene polymerisation and oligomerisation with arene-substituted phenoxy-imine complexes of titanium: investigation of multi-mechanism catalytic behaviour

Supplementary files

Article information

Article type
Paper
Submitted
20 Sep 2012
Accepted
30 Jan 2013
First published
31 Jan 2013

Dalton Trans., 2013,42, 4185-4196

Ethylene polymerisation and oligomerisation with arene-substituted phenoxy-imine complexes of titanium: investigation of multi-mechanism catalytic behaviour

J. A. Suttil, D. S. McGuinness, M. G. Gardiner and S. J. Evans, Dalton Trans., 2013, 42, 4185 DOI: 10.1039/C3DT32183E

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