Syndiospecific Living Propylene Polymerization Catalyzed by Titanium Complexes Having Fluorine-Containing Phenoxy−Imine Chelate Ligands

• Published in: Journal of the American Chemical Society 2003-04, Vol.125 (14), p.4293-4305
• Main Authors: Mitani, Makoto, Furuyama, Rieko, Mohri, Jun-ichi, Saito, Junji, Ishii, Seiichi, Terao, Hiroshi, Nakano, Takashi, Tanaka, Hidetsugu, Fujita, Terunori
• Format: Article
• Language: English
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/ja029560j

The propylene polymerization behavior of a series of Ti complexes featuring fluorine-containing phenoxy−imine chelate ligands is reported. The Ti complexes combined with methylalumoxane (MAO) can be catalysts for living and, at the same time, stereospecific polymerization of propylene at room temperature or above. DFT calculations suggest that the attractive interaction between a fluorine ortho to the imine nitrogen and a β-hydrogen of a growing polymer chain is responsible for the achievement of room-temperature living propylene polymerization. Although the Ti complexes possess C 2 symmetry, they are capable of producing highly syndiotactic polypropylenes. 13C NMR is used to demonstrate that the syndiotacticity is governed by a chain-end control mechanism and that the polymerization is initiated exclusively via 1,2-insertion followed by 2,1-insertion as the principal mode of polymerization. 13C NMR spectroscopy also elucidated that the polypropylenes produced with the Ti complexes possess regio-block structures. Substitutions on the phenoxy−imine ligands have profound effects on catalytic behavior of the Ti complexes. The steric bulk of the substituent ortho to the phenoxy oxygen plays a decisive role in achieving high syndioselectivity for the chain-end controlled polymerization. Over a temperature range of 0−50 °C, Ti complex having a trimethylsilyl group ortho to the phenoxy oxygen forms highly syndiotactic, nearly monodisperse polypropylenes (94−90% rr) with extremely high peak melting temperatures (T m = 156−149 °C). The polymerization behavior of the Ti complexes can be explained well by the recently proposed site-inversion mechanism for the formation of syndiotactic polypropylene by a Ti complex having a pair of fluorine-containing phenoxy−imine ligands.