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Bryliakov, Konstantin P., Kravtsov, Evgenii A., Broomfield, Lewis, Talsi, Evgenii P. and Bochmann, Manfred 
ORCID: https://orcid.org/0000-0001-7736-5428
(2007)
Activation of bis(pyrrolylaldiminato) and (salicylaldiminato)(pyrrolylaldiminato) titanium polymerization catalysts with methylalumoxane.
Organometallics, 26 (2).
pp. 288-293.
Abstract
Cationic intermediates formed upon activation of an olefin polymerization catalyst based on bis[N-phenylpyrrolylaldiminato]titanium(IV) dichloride (L2TiCl2, I ) and [N-(3-tert-butylsalicylidene)-2,3,4,5,6-pentafluoroanilinato-N‘-phenylpyrrolylaldiminato]titanium(IV) dichloride (L‘LTiCl2, II ) with methylalumoxane (MAO) have been identified. Outer-sphere ion pairs of the type [L2TiMe(S)]+[MeMAO]- and [L‘LTiMe(S)]+[MeMAO]- capable of ethene polymerization have been characterized by 1H and 13C NMR spectroscopy. Unlike methyl metallocenium cations, the barrier of the first ethene insertion into the Ti-Me bonds of these species is not significantly higher than that of subsequent insertions. Surprisingly, whereas homoligated catalyst precursors L2TiCl2 in the presence of MAO are prone to ligand transfer to aluminum, under the same conditions the heteroligated system L‘LTiCl2/MAO proved resistant to ligand scrambling.
| Item Type: | Article |
|---|---|
| Faculty \ School: | Faculty of Science > School of Chemistry |
| UEA Research Groups: | Faculty of Science > Research Groups > Synthetic Chemistry (former - to 2017) Faculty of Science > Research Groups > Chemistry of Light and Energy Faculty of Science > Research Groups > Chemistry of Materials and Catalysis |
| Depositing User: | Rachel Smith |
| Date Deposited: | 12 Apr 2011 13:45 |
| Last Modified: | 27 Oct 2023 00:38 |
| URI: | https://ueaeprints.uea.ac.uk/id/eprint/29051 |
| DOI: | 10.1021/om0607752 |
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