N-(5,6,7-Trihydroquinolin-8-ylidene)arylaminonickel dichlorides as highly active single-site pro-catalysts in ethylene polymerization
Yu JG(余建刚) ; Ceng YN(曾艳宁) ; Huang W(黄伟) ; Hao X(郝项) ; Sun WH(孙文华)
刊名Dalton Trans.
2011
卷号40页码:8436-8443
ISSN号1477-9226
通讯作者孙文华
中文摘要A series of N-(5,6,7-trihydroquinolin-8-ylidene)arylamine ligands was synthesized and fully characterized by NMR, IR spectroscopy and elemental analysis. Dimeric N-(5,6,7- trihydroquinolin-8-ylidene)arylaminonickel dichlorides were prepared and examined by IR spectroscopy and elemental analysis, and the molecular structures of the representative nickel complexes were determined by the single crystal X-ray diffraction. On treatment with various alkylaluminiums, all the title complexes exhibited highly active, single-site active behavior for ethylene polymerization producing polyethylene (PE) waxes. The catalytic systems using the co-catalysts diethylaluminium chloride (Et2AlCl) or methylaluminoxane (MAO) were investigated in detail, and the molecular weights and distributions of the PEs obtained were found to significantly rely on the nature of the different ligands present and reaction parameters such as the molar ratios of Al/Ni, reaction
学科主题物理化学
收录类别SCI
资助信息MOST 863 program No. 2009AA033601
语种英语
WOS记录号WOS:000293694200024
公开日期2012-09-20
内容类型期刊论文
源URL[http://210.77.64.217/handle/362003/372]  
专题兰州化学物理研究所_OSSO国家重点实验室
推荐引用方式
GB/T 7714
Yu JG,Ceng YN,Huang W,et al. N-(5,6,7-Trihydroquinolin-8-ylidene)arylaminonickel dichlorides as highly active single-site pro-catalysts in ethylene polymerization[J]. Dalton Trans.,2011,40:8436-8443.
APA 余建刚,曾艳宁,黄伟,郝项,&孙文华.(2011).N-(5,6,7-Trihydroquinolin-8-ylidene)arylaminonickel dichlorides as highly active single-site pro-catalysts in ethylene polymerization.Dalton Trans.,40,8436-8443.
MLA 余建刚,et al."N-(5,6,7-Trihydroquinolin-8-ylidene)arylaminonickel dichlorides as highly active single-site pro-catalysts in ethylene polymerization".Dalton Trans. 40(2011):8436-8443.
个性服务
查看访问统计
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。


©版权所有 ©2017 CSpace - Powered by CSpace