Teaming Up Main Group Metals with Metallic Iron to Boost Hydrogenation Catalysis
Overview
Authors
Affiliations
Hydrogenation of unsaturated bonds is a key step in both the fine and petrochemical industries. Homogeneous and heterogeneous catalysts are historically based on noble group 9 and 10 metals. Increasing awareness of sustainability drives the replacement of costly, and often harmful, precious metals by abundant 3d-metals or even main group metals. Although not as efficient as noble transition metals, metallic barium was recently found to be a versatile hydrogenation catalyst. Here we show that addition of finely divided Fe, which itself is a poor hydrogenation catalyst, boosts activities of Ba by several orders of magnitude, enabling rapid hydrogenation of alkynes, imines, challenging multi-substituted alkenes and non-activated arenes. Metallic Fe also boosts the activity of soluble early main group metal hydride catalysts, or precursors thereto. This synergy originates from cooperativity between a homogeneous, highly reactive, polar main group metal hydride complex and a heterogeneous Fe surface that is responsible for substrate activation.
Li Y, Huang A, Zhou L, Li B, Zheng M, Zhuang Z Nat Commun. 2024; 15(1):8365.
PMID: 39333097 PMC: 11436649. DOI: 10.1038/s41467-024-52494-0.
Propane dehydrogenation catalysis of group IIIB and IVB metal hydrides.
Hu X, Huang M, Kinjyo T, Mine S, Toyao T, Hinuma Y RSC Adv. 2024; 14(32):23459-23465.
PMID: 39055265 PMC: 11270002. DOI: 10.1039/d4ra02473g.
Opportunities with calcium Grignard reagents and other heavy alkaline-earth organometallics.
Harder S, Langer J Nat Rev Chem. 2023; 7(12):843-853.
PMID: 37935796 DOI: 10.1038/s41570-023-00548-0.