Abstract
The N-substituents on the backbone of Ph2PN(R)Si(CH3)2CH2PPh2- and [Ph2PCH2Si(CH3)2]2N(R)-type silylated-diphosphinoamine (Si-PNP) systems have been observed to have a significant impact on their catalytic performance in ethylene oligomerization reactions. Cr precatalyst 3, bearing an isopropyl (iPr) substituent, affords the most efficient catalytic system and exhibited the highest selectivity (83%) toward 1-octene (1-C8) and showed a catalytic activity of more than 76,700 g(product)·g(Cr)−1·h–1 under experimental conditions. Single-crystal analysis results revealed the influence of steric constraints around the catalytically active center and established a relationship between the product selectivity and the P–Cr–P bite angle. Furthermore, DFT calculations indicate that the catalytic system based on precatalyst 3 faces a low energy barrier in the formation of 1-C8 and therefore shows high selectivity toward the 1-C8 fraction. Modification in the backbone length may alter the binding mode of the ligands f...
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.