Dehydrogenation of formic acid mediated by a Phosphorus–Nitrogen PN3P-manganese pincer complex: Catalytic performance and mechanistic insights
Alobaid, Nasser A.
Menicucci, Fabio Lorenzo
KAUST DepartmentChemical Science Program
Homogeneous Catalysis Laboratory (HCL)
KAUST Catalysis Center (KCC)
Physical Science and Engineering (PSE) Division
Embargo End Date2024-05-16
Permanent link to this recordhttp://hdl.handle.net/10754/677977
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AbstractThe utilization of formic acid as a liquid organic hydrogen carrier has taken a vast interest lately because of several desirable properties. The state-of-the-art homogenous catalysts known for formic acid dehydrogenation are mainly based on noble metals such as iridium or ruthenium. 3d metals are considered to be an attractive alternative due to their abundance and low toxicity. Exploration of 3d metals has achieved exciting results mainly with iron-based catalysts; however, manganese has not received much attention, and only a few examples are available. Here we report a manganese complex [Mn(PN3P)(CO)2]Br containing a pincer backbone, as an efficient catalyst for formic acid dehydrogenation. Under the optimized condition, the complex afforded a TON of 15,200. To the best of our knowledge, this is considered one of the best TON achieved using a manganese-based complex with excellent selectivity. Mechanistic studies suggested that the imine arm participates in the formic acid activation/deprotonation step, emphasizing the importance of metal-ligand cooperativity during substrate activation to promote catalytic efficacy.
CitationDutta, I., Alobaid, N. A., Menicucci, F. L., Chakraborty, P., Guan, C., Han, D., & Huang, K.-W. (2022). Dehydrogenation of formic acid mediated by a Phosphorus–Nitrogen PN3P-manganese pincer complex: Catalytic performance and mechanistic insights. International Journal of Hydrogen Energy. https://doi.org/10.1016/j.ijhydene.2022.04.220
SponsorsFinancial support is provided by King Abdullah University of Science and Technology (KAUST).