Journal
JOURNAL OF ORGANOMETALLIC CHEMISTRY
Volume 980-981, Issue -, Pages -Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jorganchem.2022.122508
Keywords
Olefin metathesis; Electron -withdrawing group; Initiation rate
Categories
Funding
- National Science centre grant Beethoven 2
- [UMO-2016/23/G/ST5/04297]
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This study investigates the initiation rates of ruthenium metathesis catalysts by introducing various modifications. The results show that catalysts with electron-withdrawing substituents in the benzylidene part can achieve very fast initiation, with -SO2C4F9 derivatives being the most effective initiators.
The initiation rate of ruthenium metathesis catalysts is one of their most important characteristics from the applicational point of view due to the fact, that initiation is often the rate-limiting step of the entire catalytic cycle. Such initiation rate can be adjusted by introducing various modifications to the commonly used Grubbs-like and Hoveyda-Grubbs-like catalysts. Using a DFT approach, we predicted the initiation rates of the 2nd generation Hoveyda-Grubbs catalyst analogues substituted with electron-withdrawing -NO, -NO2, and -SO2C4F9 groups in all positions of the phenyl ring in the benzylidene part. We show that some of the modifications should result in very fast-initiating catalysts. In particular, the -SO2C4F9- substitued derivatives are predicted to be the fastest-initiating in the series. We also found correla-tions between the selected computed parameters such as the Gibbs free energy barrier for initiation and ruthenium-oxygen bond strengths which, combined with distortion energy analysis, allowed us to provide an explanation of the main driving force behind fast initiation. (c) 2022 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )
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