Wang Wei, Fujiki Michiya, Nomura Kotohiro
Graduate School of Materials Science, Nara Institute of Science and Technology (NAIST), 8916-5 Takayama, Ikoma, Nara 630-0101, Japan.
J Am Chem Soc. 2005 Apr 6;127(13):4582-3. doi: 10.1021/ja050274s.
Cyclohexene (CHE) has been incorporated into the polymer chain in ethylene/CHE copolymerization by nonbridged half-titanocenes containing aryloxo ligands of the type, Cp'TiCl2(O-2,6-iPr2C6H3), in the presence of methylaluminoxane (MAO) cocatalyst. The effect of the substituent in the cyclopentadienyl fragment was found to be very important for CHE incorporation; both the tert-BuCp (3) and 1,2,4-Me3Cp analogues (4) showed efficient CHE incorporation, whereas a negligible amount of CHE incorporation was observed by both the indenyl (1) and the Cp* analogue (2) under the same conditions. Cp-ketimide analogue, CpTiCl2(N=CtBu2) (5), zirconocene-like Cp2ZrCl2 (6), and linked half-titanocene-like [Me2Si(C5Me4)(NtBu)]TiCl2 (7) did not show any CHE incorporation under the same conditions; unique characteristics for using this type of catalyst precursor for the present copolymerization have thus been emphasized.
在甲基铝氧烷(MAO)助催化剂存在下,通过含有Cp'TiCl2(O-2,6-iPr2C6H3) 类型芳氧基配体的非桥联半钛茂,环己烯(CHE)已被引入乙烯/CHE共聚反应的聚合物链中。发现环戊二烯基片段中的取代基对CHE的引入非常重要;叔丁基环戊二烯基(3)和1,2,4-三甲基环戊二烯基类似物(4)都显示出高效的CHE引入,而在相同条件下,茚基(1)和五甲基环戊二烯基类似物(2)观察到的CHE引入量可忽略不计。在相同条件下,环戊二烯基酮亚胺类似物CpTiCl2(N=CtBu2)(5)、类锆茂Cp2ZrCl2(6)和连接的类半钛茂[Me2Si(C5Me4)(NtBu)]TiCl2(7)均未显示出任何CHE引入;因此强调了使用这种类型的催化剂前体进行本共聚反应的独特特性。