Preparation of new dinuclear half-titanocene complexes with ortho- and meta-xylene linkages and investigation of styrene polymerization

摘要

Half-titanocene is well-known as an excellent catalyst for the preparation of SPS (syndiotactic polystyrene) when activated with methylaluminoxane (MAO). Dinuclear half-sandwich complexes of titanium bearing a xylene bridge, (TiCl2L)(2){(mu-eta(5), eta(5)-C5H4-ortho-(CH2-C6H4-CH2)C5H4}, (4 (L = Cl), 7 (L = O-2,6-iPr(2)C(6)H(3))) and (TiCl2L)(2){(mu-eta(5), eta(5)-C5H4-meta-(CH2-C6H4-CH2)C5H4} (5(L = Cl), 8(L = O-2,6-iPr(2)C(6)H(3))), have been successfully synthesized and introduced for styrene polymerization. The catalysts were characterized by H-1- and C-13 NMR, and elemental analysis. These catalysts were found to be effective in forming SPS in combination with MAO. The activities of the catalysts with rigid ortho- and meta-xylene bridges were higher than those of catalysts with flexible pentamethylene bridges. The catalytic activity of four dinuclear half-titanocenes increased in the order of 4 < 5 < 7 < 8. This result displays that the meta-xylene bridged catalyst is more active than the ortho- xylene bridged and that the aryloxo group at the titanium center is more effective at promoting catalyst activity compared to the chloride group at the titanium center. Temperature and ratio of [Al]:[Ti] had significant effects on catalytic activity. Polymerizations were conducted at three different temperatures (25, 40, and 70 degrees C) with variation in the [Al]:[Ti] ratio from 2000 to 4000. It was observed that activity of the catalysts increased with increasing temperature, as well as higher [Al]:[Ti]. Different xylene linkage patterns (ortho and meta) were recognized to be a principal factor leading to the characteristics of the dinuclear catalyst due to its different spatial arrangement, causing dissimilar intramolecular interactions between the two active sites.