Cooperative hydrogenation catalysis at a constrained gallylene-nickel(0) interface

The discovery of unique mechanisms in 3d metal catalysis is of paramount importance in utilizing these Earth-abundant metals in place of scarce precious metals. Inspired by the Horiuti-Polanyi mechanism at play in heterogeneous hydrogenation catalysts, we describe a bimetallic molecular catalyst tha...

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Detalles Bibliográficos
Autores: Kalkuhl, Till, Fernández López, Israel, Hadlington, Terrance
Tipo de recurso: artículo
Fecha de publicación:2025
País:España
Institución:Universidad Complutense de Madrid (UCM)
Repositorio:Docta Complutense
Idioma:inglés
OAI Identifier:oai:docta.ucm.es:20.500.14352/120252
Acceso en línea:https://hdl.handle.net/20.500.14352/120252
Access Level:acceso abierto
Palabra clave:547
Cooperative catalysis
Bimetallic catalysis
Hydrogen activation
Metallo-ligands
Gallylene ligand
Small molecule activation
Sustainable catalysis
Novel mechanisms
Kinetic analysis
Reversible activation
Química
23 Química
Descripción
Sumario:The discovery of unique mechanisms in 3d metal catalysis is of paramount importance in utilizing these Earth-abundant metals in place of scarce precious metals. Inspired by the Horiuti-Polanyi mechanism at play in heterogeneous hydrogenation catalysts, we describe a bimetallic molecular catalyst that can selectively semi-hydrogenate alkynes via a ligand-to-substrate hydride transfer mechanism. This mimics established heterogeneous mechanisms in which remote surface-bound hydride ligands undergo a similar reactive process. This is achieved through the development of a chelate-constrained gallium(I) ligand, which operates in concert with nickel(0) to (reversibly) cleave H2, generating a [GaNi] 1,2-dihydride complex that is found to be the resting state in the catalytic process. This discovery takes steps toward utilizing non-innocent low-valent group 13 centers in effective cooperative catalysis, opening new mechanistic pathways that may aid in employing Earth-abundant metals in key catalytic transformations