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α-olefin homopolymerization and ethylene/1-hexene copolymerization catalysed by novel ansa-group IV complexes/MAO system  ( EI收录)  

文献类型:期刊文献

英文题名:α-olefin homopolymerization and ethylene/1-hexene copolymerization catalysed by novel ansa-group IV complexes/MAO system

作者:Yang, Xiaoxia[1]; Zhang, Yong[1]; Huang, Jiling[1]

机构:[1] Laboratory of Organometallic Chemistry, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China

年份:2007

卷号:21

期号:10

起止页码:870

外文期刊名:Applied Organometallic Chemistry

收录:EI(收录号:20074510904039)

语种:英文

外文关键词:Catalyst activity - Copolymerization - Homopolymerization - Polypropylenes

摘要:The catalytic properties of a set of ansa-complexes (R-Ph) 2C(Cp)(Ind)MCl2 [R =tBu, M = Ti (3), Zr (4) or Hf (5); R = MeO, M = Zr (6), Hf (7)] in α-olefin homopolymerization and ethylene/1-hexene copolymerization were explored in the presence of MAO (methylaluminoxane). Complex 4 with steric bulk tBu group on phenyl exhibited remarkable catalytic activity for ethylene polymerization. It was 1.6-fold more active than complex 11 [Ph2C(Cp)(Ind)ZrCl2] at 11 atm ethylene pressure and was 4.8-fold more active at 1 atm pressure. The introduction of bulk substituent tBu into phenyl groups not only increased the catalytic activity greatly but also enhanced the content of 1-hexene in ethylene/1 -hexene copolymerization. The highest 1-hexene incorporation was 25.4%. In addition, 4 was also active for propylene and 1-hexene homopolymerization, respectively, and low isotactic polypropylene (mmmm = 11.3%) and isotactic polyhexene (mmmm = 31.6%) were obtained. Copyright ? 2007 John Wiley & Sons, Ltd.

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