Tuning a Cr-Catalyzed Ethylene Oligomerization Product Profile via a Rational Design of the N-aryl PNP Ligands

Catalysts Pub Date : 2024-07-10 DOI:10.3390/catal14070441
Samir Barman, E. Jaseer, Nestor Garcia, Mohamed Elanany, Motaz Khawaji, Niladri Maity, Abdulrahman Musa
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Abstract

An approach towards incorporating varied degrees of steric profiles around the ligand’s backbone, which were envisaged to alter the catalytic paths leading to targeted 1-C8/1-C6 olefin products, were explored. Cr-pre-catalysts designed with PNP ligands comprising a fused aryl moiety were delivered at a relatively higher C8 olefin selectivity (up to 74.6 wt% and C8/C6 of 3.4) when the N-connection to the aromatic unit was placed at the 2-position. A relatively higher C6 olefin selectivity (up to 33.7 wt% and C8/C6 of 1.9) was achieved with the PNP unit anchored at the 1- or 6-position. Based on detailed catalytic studies, we confirm the fact that by introducing a controlled degree of bulkiness on the N-site through a judicious selection of the N-aryl moiety of different sizes, the selectivity of the targeted olefin product could be tuned in a rational manner.
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通过合理设计 N-芳基 PNP 配体调谐铬催化乙烯低聚产物谱
我们探索了在配体骨架周围加入不同程度立体剖面的方法,以改变催化路径,从而催化出目标 1-C8/1-C6 烯烃产物。当与芳香单元的 N 连接位于 2 位时,使用包含融合芳基的 PNP 配体设计的 Cr 预催化剂可提供相对较高的 C8 烯烃选择性(高达 74.6 wt%,C8/C6 为 3.4)。当 PNP 单元锚定在 1 位或 6 位时,C6 烯烃选择性相对较高(高达 33.7 wt%,C8/C6 为 1.9)。基于详细的催化研究,我们证实了这样一个事实:通过明智地选择不同大小的 N 芳基,在 N 位上引入可控的松散度,可以合理地调整目标烯烃产物的选择性。
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