| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1328592 | Journal of Organometallic Chemistry | 2006 | 5 Pages |
A series of titanium phosphinimide complexes [Ph2P(2-RO-C6H4)]2TiCl2 (7, R = CH3; 8, R = CHMe2) and [PhP(2-Me2CHO–C6H4)][THF]TiCl3 (9) have been prepared by reaction of TiCl4 with the corresponding phosphinimines under dehalosilylation. The structure of complex 9 has been determined by X-ray crystallography, and a solvent molecule THF was found to be coordinated with the central metal and the Ti–O bond was consistent with the normal Ti–O (donor) bond length. The complexes 7 and 8 displayed inactive to ethylene polymerization, and the complex 9 displayed moderate activity in the presence of modified methylaluminoxane (MMAO) or i-Bu3Al/Ph3CB(C6F5)4, and this should be partly attributed to coordination of THF with titanium and the steric effect of two iso-propoxyl. And catalytic activity up to 32.2 kg-PE/(mol-Ti h bar) was observed.
Graphical abstractA series of triaryl-substituted phosphinimide titanium complexes have been prepared by reaction of TiCl4 with the corresponding phosphinimines. Complex 9 displayed moderate activity in the presence of MMAO or i-Bu3Al/Ph3CB(C6F5)4, and this should be partly attributed to coordination of THF with titanium and the steric effect of two iso-propoxyl. And catalytic activity up to 32.2 kg-PE/(mol-Ti h bar) was observed.Figure optionsDownload full-size imageDownload as PowerPoint slide
