甲基铝氧烷
铬
乙烯
催化作用
选择性
化学
配体(生物化学)
1-辛烯
密度泛函理论
高分子化学
立体化学
组合化学
有机化学
计算化学
茂金属
受体
生物化学
聚合物
聚合
作者
Xiangyang Meng,Zhiqiang Ding,Huan Xin Gao,Zhe Ma,Li Pan,Bin Wang,Yue‐Sheng Li
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2024-05-06
卷期号:29 (9): 2158-2158
被引量:6
标识
DOI:10.3390/molecules29092158
摘要
A series of novel binuclear PNP ligands based on the cyclohexyldiamine scaffold were synthesized for this study. The experimental results showed that positioning the two PNP sites at the para-positions of the cyclohexyl framework led to a significant enhancement in the catalytic activity for selective tri/tetramerization of ethylene. The PNP/Cr(acac)3/MAO(methylaluminoxane) catalytic system exhibited relatively high catalytic activity (up to 3887.7 kg·g−1·h−1) in selective ethylene oligomerization with a total selectivity of 84.5% for 1-hexene and 1-octene at 40 °C and 50 bar. The relationship between the ligand structure and ethylene oligomerization performance was further explored using density functional theory calculations.
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