| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1326506 | Journal of Organometallic Chemistry | 2012 | 6 Pages |
Permethylated cyclopentadienyl dinuclear constrained geometry titanium catalyst, [μ-(C6H4)2-2,2′]{(η5-C5Me3)[1-Me2Si(η1-N-tBu)](TiCl2)}2 (BPTi2) linked by a biphenylene bridge was synthesized and tested in ethylene and ethylene/1-octene polymerizations upon activation by TIBA (triisobutylaluminum)/[Ph3C][B(C6F5)4]. When compared with the corresponding highly active, mononuclear analogs, Me2Si(η5-2-PhC5Me3)(η1-N-tBu)TiCl2 (PhTi1) and Me2Si(η5-C5Me4)(η1-N-tBu)TiCl2 (MeTi1), BPTi2 exhibits significantly increased molecular weight of polymer (>two-fold), as well as high level of activity and 1-octene incorporations in ethylene and ethylene/1-octene polymerizations. Although the lower activity was observed at high 1-octene feeds, the combined effects of rigidity and electronic conjugation induced by the biphenylene bridge might be responsible for the observed polymerization properties of BPTi2.
Graphical abstractPermethylated cyclopentadienyl dinuclear Ti-CGC linked by a biphenylene bridge exhibits significantly increased molecular weight, as well as high activity and high 1-octene incorporation in ethylene and ethylene/1-octene polymerizations in comparison with the corresponding mononuclear CGC analogs.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Synthesis of a novel permethylated cyclopentadienyl dinuclear Ti-CGC. ► Significant increase in MW of polyethylene and poly(ethylene-co-1-octene). ► Retention of high level of activity and 1-octene incorporation.
