A Well‐Defined, Air‐Stable NHC–Ni Precatalyst for C–N Bond Formation

A new, well-defined, air-stable N-heterocyclic carbene nickel(II) precatalyst [(IPr)Ni(N-methylphenethylamine)Cl] (IPr = N,N'-bis(2,6-diisopropylphenyl)imidazol-2-ylidene) was designed, synthesized, and evaluated for C-N cross-coupling reactions. This precatalyst is readily activated in the presence of base and efficiently promotes the amination of a variety of aryl chlorides with amines. Optimization studies established robust reaction conditions and revealed the influence of electronic and steric properties of the coupling partners on catalytic performance. The combination of operational simplicity, long-term bench stability, and facile activation makes this NHC-Ni precatalyst a good choice for nickel-catalyzed C-N bond formation.

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Publication Details

Journal
Chemistry - A European Journal
Published
2026-09-29
DOI
https://doi.org/10.1002/chem.71749
Primary Topic
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
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article
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A Well‐Defined, Air‐Stable NHC–Ni Precatalyst for C–N Bond Formation

Jürgen Schulmeister, Kianoosh Masoomi, Michael G. Organ
Chemistry - A European Journal
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
article

A Well‐Defined, Air‐Stable NHC–Ni Precatalyst for C–N Bond Formation

Jürgen Schulmeister, Kianoosh Masoomi, Michael G. Organ
article en

Abstract

A new, well-defined, air-stable N-heterocyclic carbene nickel(II) precatalyst [(IPr)Ni(N-methylphenethylamine)Cl] (IPr = N,N'-bis(2,6-diisopropylphenyl)imidazol-2-ylidene) was designed, synthesized, and evaluated for C-N cross-coupling reactions. This precatalyst is readily activated in the presence of base and efficiently promotes the amination of a variety of aryl chlorides with amines. Optimization studies established robust reaction conditions and revealed the influence of electronic and steric properties of the coupling partners on catalytic performance. The combination of operational simplicity, long-term bench stability, and facile activation makes this NHC-Ni precatalyst a good choice for nickel-catalyzed C-N bond formation.

Chemistry - A European Journal
University of Ottawa (CA), Centre for Catalysis Research and Innovation
Clean water and sanitation
Openalex Percentile: Top 22%
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
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A Well‐Defined, Air‐Stable NHC–Ni Precatalyst for C–N Bond Formation — Jürgen Schulmeister, Kianoosh Masoomi, et al. · Chemistry - A European Journal (2026) | TGRS Research Map | TGRS