详细信息
α-olefin homopolymerization and ethylene/1-hexene copolymerization catalysed by novel ansa-group IV complexes/MAO system ( SCI-EXPANDED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; Zhang, Yong; Huang, Jiling
机构:[1]E China Univ Sci & Technol, Organomet Chem Lab, Shanghai 200237, Peoples R 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:;WOS:【SCI-EXPANDED(收录号:WOS:000250629100008)】;
语种:英文
外文关键词:ansa-metallocene; alpha-olefin; ethylene polymerization; copolymerization
摘要:The catalytic properties of a set of ansa-complexes (R-Ph)(2)C(Cp)(Ind)MCl2 [R =Bu-t, M = Ti (3), Zr (4) or Hf (5); R = MeO, M = Zr (6), Hf (7)] in a-olefin homopolymerization and ethylene/1-hexene copolymerization were explored in the presence of MAO (methylaluminoxane). Complex 4 with steric bulk Bu-t 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 (C) 2007 John Wiley & Sons, Ltd.
参考文献:
正在载入数据...
