Journal
DALTON TRANSACTIONS
Volume 51, Issue 42, Pages 16215-16223Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2dt02597c
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Funding
- NSFC [22163001, 21803014]
- Natural Science Foundation of Guangxi [AD19110101]
- key project of Guangxi Normal University [2017ZD001]
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This study investigates the mechanistic preference of a ruthenium complex with dual proton-responsive sites in borrowing-hydrogen N-alkylation catalysis using DFT calculations. The results suggest that the gamma-NH site facilitates the rate-determining step via non-covalent interaction, while the alpha-NH site requires overcoming a higher activation energy barrier.
Metal-ligand cooperation (MLC) catalysis is one of the most important concepts in the field of organometallic catalysis. However, diverse functional ligands result in ambiguous mechanisms and constrain the understanding of MLC catalysis. Herein, a theoretical study based on DFT calculations is performed to shed light on the mechanistic preference of borrowing-hydrogen N-alkylation catalysed by a ruthenium complex with dual proton-responsive sites. The results suggest that the reaction pathway mediated by the alpha-NH site requires overcoming a higher activation energy barrier (31.4 kcal mol(-1)) compared with the gamma-NH site due to the ligand distortion after protonation. Nevertheless, the instability caused by the ligand distortion does not transform into catalytic activity for the subsequent hydrogenation reaction. In contrast, the gamma-NH site facilitates the rate-determining hydride transfer step (21.1 kcal mol(-1)) via non-covalent interaction instead of participating in the bond formation and breaking process, which is found to be a more plausible mechanism. These findings demonstrate the versatile role of ligand N-H functionality, which may provide useful guidance for the design of new MLC catalysts in the future.
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