Advances in Ni <sup>I</sup> /Ni <sup>III</sup> -Catalyzed C(sp <sup>2</sup> )–Heteroatom Cross-Couplings

C-(sp<sup>2</sup>)-heteroatom couplings operating via Ni<sup>I</sup>/Ni<sup>III</sup> catalysis have emerged as an alternative to canonical Pd<sup>0</sup>/Pd<sup>II</sup> systems that require complex ligand architectures. Despite intensive research efforts during the past decade, catalytic methods employing this approach are still mostly confined to activated starting materials and require high catalyst loadings due to the low catalytic activity of Ni<sup>I</sup> and undesired catalyst deactivation events. This article highlights recent advances in the field toward solving these long-standing challenges. We survey strategies that streamline the generation of catalytically competent Ni<sup>I</sup> species from bench-stable Ni<sup>II</sup> precatalysts, and discuss mechanistic studies that shed light on deactivation pathways and the rate-determining oxidative addition of aryl halides. In the final section, we highlight recently developed synthetic methodologies, which provide evidence that limitations can indeed be addressed by working at elevated temperatures, employing alternative electrophiles, harnessing the benefits of additives, or fine-tuning the metal's reactivity through the ligand field.

Authors

Institutions

Publication Details

Journal
ACS Catalysis
Published
2025-12-24
DOI
https://doi.org/10.1021/acscatal.5c07964
Citations
1
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
0.94
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Advances in Ni I /Ni III -Catalyzed C(sp 2 )–Heteroatom Cross-Couplings

Bartholomäus Pieber, Aleksander R. Bena
1 citations
ACS Catalysis
Catalytic Cross-Coupling Reactions
0.94
article

Advances in Ni I /Ni III -Catalyzed C(sp 2 )–Heteroatom Cross-Couplings

Bartholomäus Pieber, Aleksander R. Bena
article en
1 citations

Abstract

C-(sp<sup>2</sup>)-heteroatom couplings operating via Ni<sup>I</sup>/Ni<sup>III</sup> catalysis have emerged as an alternative to canonical Pd<sup>0</sup>/Pd<sup>II</sup> systems that require complex ligand architectures. Despite intensive research efforts during the past decade, catalytic methods employing this approach are still mostly confined to activated starting materials and require high catalyst loadings due to the low catalytic activity of Ni<sup>I</sup> and undesired catalyst deactivation events. This article highlights recent advances in the field toward solving these long-standing challenges. We survey strategies that streamline the generation of catalytically competent Ni<sup>I</sup> species from bench-stable Ni<sup>II</sup> precatalysts, and discuss mechanistic studies that shed light on deactivation pathways and the rate-determining oxidative addition of aryl halides. In the final section, we highlight recently developed synthetic methodologies, which provide evidence that limitations can indeed be addressed by working at elevated temperatures, employing alternative electrophiles, harnessing the benefits of additives, or fine-tuning the metal's reactivity through the ligand field.

ACS CatalysisVol. 16(2)
Institute of Science and Technology Austria (AT)
Openalex Percentile: Top 19%
Catalytic Cross-Coupling Reactions
0.94
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.