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Catalytic Trimerization of Ethylene with Highly Active Half-sandwich Titanium Complexes Bearing Pendant p-Fluorophenyl Groups    

Catalytic Trimerization of Ethylene with Highly Active Half-sandwich Titanium Complexes Bearing Pendant p-Fluorophenyl Groups

文献类型:期刊文献

中文题名:Catalytic Trimerization of Ethylene with Highly Active Half-sandwich Titanium Complexes Bearing Pendant p-Fluorophenyl Groups

英文题名:Catalytic Trimerization of Ethylene with Highly Active Half-sandwich Titanium Complexes Bearing Pendant p-Fluorophenyl Groups

作者:王晨[1];黄吉玲[1]

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

年份:2006

卷号:24

期号:10

起止页码:1397

中文期刊名:Chinese Journal of Chemistry

外文期刊名:中国化学(英文版)

收录:CSTPCD;;Scopus;CSCD:【CSCD2011_2012】;

基金:Project supported by the National Natural Science Foundation of China (No. 20372022) and the Major State Basic Research Development Program of China (No. 2005CB623801).

语种:中文

中文关键词:ethylene;trimerization;coordination;cyclopentadienyl;titanium

外文关键词:ethylene, trimerization, coordination, cyclopentadienyl, titanium

摘要:Two new complexes [η^5-C5H4CMe2-(p-fluorophenyl)]TiCL3 (1) and [η^5-C4h4C(cyclo-C5H10)-(p-fluorophenyl)]TiCl3 (2) were synthesized and characterized. Their activities and selectivities for trimerization of ethylene were investigated. The introduction of fluorine atom greatly weakened the arene coordination, but this disadvantageous factor can be eliminated by introduction of a bulky substituent, such as cyclo-C5H10, to the bridging carbon linked to the Cp ring. The combinative effect of the fluorine substitute and the bridging unit can make complex 2 as a highly active and selective catalyst for ethylene trimerization. Its productivity and selectivity for 1-hexene can reach 1024.0 kg·mol^-1·h^-1 and 99.3% respectively.
Two new complexes [η^5-C5H4CMe2-(p-fluorophenyl)]TiCL3 (1) and [η^5-C4h4C(cyclo-C5H10)-(p-fluorophenyl)]TiCl3 (2) were synthesized and characterized. Their activities and selectivities for trimerization of ethylene were investigated. The introduction of fluorine atom greatly weakened the arene coordination, but this disadvantageous factor can be eliminated by introduction of a bulky substituent, such as cyclo-C5H10, to the bridging carbon linked to the Cp ring. The combinative effect of the fluorine substitute and the bridging unit can make complex 2 as a highly active and selective catalyst for ethylene trimerization. Its productivity and selectivity for 1-hexene can reach 1024.0 kg·mol^-1·h^-1 and 99.3% respectively.

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