位阻效应
化学
选择性
铬
乙烯
催化作用
配体(生物化学)
芳基
电子效应
活动中心
药物化学
立体化学
有机化学
受体
生物化学
烷基
作者
Xing Ling Zhao,Jihe Wang,Dongchang Liu,Weihuan Kong,Jun Zhang
出处
期刊:ACS omega
[American Chemical Society]
日期:2023-09-12
卷期号:8 (38): 34549-34556
被引量:4
标识
DOI:10.1021/acsomega.3c03356
摘要
High Resolution Image Download MS PowerPoint Slide A new class of highly active ethylene tri-/tetramerization chromium catalysts supported by iminophosphine ligands has been studied. The impact of electronic and steric changes of these ligands on selectivity and activity has been investigated by varying P - and/or N -substituents. Upon activation with MMAO, the ligand bearing a P -cyclohexyl group displayed a high activity of 307 kg/(g Cr/h) with a high trimerization selectivity of 92.6%. Decreasing the steric hindrance of N -aryl group led to a decrease in 1-hexene selectivity (74.5%), producing more 1-octene (10.3%). X-ray diffraction analysis verifies that the ligands coordinate with the chromium center in a κ 2 -P,N mode.
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