Scope and Mechanism of Nickel-Isocyanide-Catalyzed Imine Hydrosilylation for ALD-Relevant Aminosilanes

fragment facilitates ligand-to-ligand hydride transfer between silane and imine as the key mechanistic step for imine hydrosilylation.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-05-01
DOI
https://doi.org/10.1021/jacs.5c23403
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
0.00
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article

Scope and Mechanism of Nickel-Isocyanide-Catalyzed Imine Hydrosilylation for ALD-Relevant Aminosilanes

Ronald M. Pearlstein, Joshua S. Figueroa, Matthew R. MacDonald, Daniel P. Spence et al.
Journal of the American Chemical Society
Organoboron and organosilicon chemistry
article

Scope and Mechanism of Nickel-Isocyanide-Catalyzed Imine Hydrosilylation for ALD-Relevant Aminosilanes

Ronald M. Pearlstein, Joshua S. Figueroa, Matthew R. MacDonald, Daniel P. Spence, John F. Lehmann, Sean P. Dunphy
article en

Abstract

fragment facilitates ligand-to-ligand hydride transfer between silane and imine as the key mechanistic step for imine hydrosilylation.

Journal of the American Chemical Society
Maria College (US), University of California San Diego (US), Palomar College (US)
Clean water and sanitation
Openalex Percentile: Top 12%
Organoboron and organosilicon chemistry
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