Zhang Hao, Nomura Kotohiro
Graduate School of Materials Science, Nara Institute of Science and Technology, 8916-5 Takayama, Ikoma, Nara 630-0101, Japan.
J Am Chem Soc. 2005 Jul 6;127(26):9364-5. doi: 10.1021/ja052198z.
The copolymerization of ethylene with styrene by CpTiCl2(N=CtBu2) (Cp = C5Me5) took place in a living manner in the presence of methylaluminoxane (MAO) cocatalyst, although the homopolymerization of neither ethylene nor styrene proceeded in a living manner. Both the cyclopentadienyl fragment (Cp') and the anionic donor ligand (X) in Cp'TiCl2(X) directly affect the copolymerization behavior, the catalytic activities, as well as the styrene incorporation; only the above set showed a living copolymerization. No styrene repeating units were observed in the resultant poly(ethylene-co-styrene)s, suggesting that a certain degree of the styrene insertion inhibited the chain transfer in this catalysis.
在甲基铝氧烷(MAO)助催化剂存在下,CpTiCl2(N=CtBu2)(Cp = C5Me5)引发乙烯与苯乙烯的共聚反应呈现活性聚合特征,尽管乙烯和苯乙烯的均聚反应均未呈现活性聚合特征。Cp'TiCl2(X)中的环戊二烯基片段(Cp')和阴离子给体配体(X)均直接影响共聚行为、催化活性以及苯乙烯的插入率;只有上述组合表现出活性共聚。在所得的聚(乙烯-共-苯乙烯)中未观察到苯乙烯重复单元,这表明一定程度的苯乙烯插入抑制了该催化反应中的链转移。