Litcius/Paper detail

Amplifying Reactivity of Metal Hydrides: A Heterotrimetallic NiAl <sub>2</sub> (μ <sup>2</sup> -H) <sub>2</sub> Catalyst for the Dearomatization of <i>N</i> -Heterocycles

Edgardo De Leon, Fernando Gonzalez, Preetika Bauskar, Sergio Gonzalez-Eymard, David De Los Santos, Manar M. Shoshani

2023Organometallics16 citationsDOI

Abstract

Identifying methods to modulate the reactivity of metal hydrides is lacking yet highly desirable given the role they play in a plethora of catalytic applications. Herein we report novel methodology to amplify the reactivity of metal hydrides through the design of well-defined heterometallic bridged hydride species. Catalytic hydroboration of quinolines was dramatically altered by the addition of a secondary metal to bridge the Al–hydride species LAlH . Specifically, the addition of Ni(COD) 2 led to the formation of novel heterotrimetallic species 1 which features Ni participating in 3-center bonding with sterically accessible Al–H species and exhibits catalytic hydroboration of sterically encumbered quinolines and approximately a 400 times enhancement in catalytic reactivity in comparison to LAlH .

Topics & Concepts

ChemistryReactivity (psychology)HydroborationSteric effectsCatalysisHydrideMetalCombinatorial chemistryMedicinal chemistryStereochemistryOrganic chemistryPathologyAlternative medicineMedicineAsymmetric Hydrogenation and CatalysisOrganoboron and organosilicon chemistryCatalytic Cross-Coupling Reactions