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.
| Original language | English |
|---|---|
| Article number | 441 |
| Journal | Catalysts |
| Volume | 14 |
| Issue number | 7 |
| DOIs | |
| State | Published - Jul 2024 |
Bibliographical note
Publisher Copyright:© 2024 by the authors.
Keywords
- catalysis
- chromium
- ethylene
- octene
- oligomerization
ASJC Scopus subject areas
- Catalysis
- General Environmental Science
- Physical and Theoretical Chemistry