A Bench‐Stable Fluorophosphine Nickel(0) Complex and Its Catalytic Application

Abstract We herein present a fluorophosphine‐based nickel(0) complex [Ni(PFPh 2 ) 4 ] ( 1 ), which is highly stable in air and water. [Ni(PFPh 2 ) 4 ] can be obtained from a one‐pot reaction of [Ni(MeCN) 4 ](BF 4 ) 2 with Ph 2 P(═O)–PPh 2 , involving a unique in situ reduction of Ni(II) to Ni(0) and a simultaneous fluorination by the BF 4 − anion. This complex does not only incorporate a nickel center in the zero‐oxidation state, resulting from a Ni(II) precursor, but also includes fluorophosphine ligands, which typically disproportionate immediately in solution. The application of [Ni(PFPh 2 ) 4 ] as highly stable Ni(0) pre‐catalyst in combination with additional phosphine ligands, such as dppf (1,1′‐bis(diphenylphosphino)ferrocene), in various coupling reactions uncovers its high catalytic activity and versatility, which is superior to [Ni(COD) 2 ] (COD═cycloocta‐1,5‐diene) as conventional Ni(0) source.

Authors

Institutions

Publication Details

Journal
Angewandte Chemie
Published
2025-04-09
DOI
https://doi.org/10.1002/ange.202506271
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A Bench‐Stable Fluorophosphine Nickel(0) Complex and Its Catalytic Application

Arjun Neyyathala, Toni Grell, Franziska Flecken, Schirin Hanf
Angewandte Chemie
Asymmetric Hydrogenation and Catalysis
article

A Bench‐Stable Fluorophosphine Nickel(0) Complex and Its Catalytic Application

Arjun Neyyathala, Toni Grell, Franziska Flecken, Schirin Hanf
article en

Abstract

Abstract We herein present a fluorophosphine‐based nickel(0) complex [Ni(PFPh 2 ) 4 ] ( 1 ), which is highly stable in air and water. [Ni(PFPh 2 ) 4 ] can be obtained from a one‐pot reaction of [Ni(MeCN) 4 ](BF 4 ) 2 with Ph 2 P(═O)–PPh 2 , involving a unique in situ reduction of Ni(II) to Ni(0) and a simultaneous fluorination by the BF 4 − anion. This complex does not only incorporate a nickel center in the zero‐oxidation state, resulting from a Ni(II) precursor, but also includes fluorophosphine ligands, which typically disproportionate immediately in solution. The application of [Ni(PFPh 2 ) 4 ] as highly stable Ni(0) pre‐catalyst in combination with additional phosphine ligands, such as dppf (1,1′‐bis(diphenylphosphino)ferrocene), in various coupling reactions uncovers its high catalytic activity and versatility, which is superior to [Ni(COD) 2 ] (COD═cycloocta‐1,5‐diene) as conventional Ni(0) source.

Angewandte ChemieVol. 137(24)
Karlsruhe Institute of Technology (DE), University of Milan (IT)
Openalex Percentile: Top 94%
Asymmetric Hydrogenation and Catalysis
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.

A Bench‐Stable Fluorophosphine Nickel(0) Complex and Its Catalytic Application — Arjun Neyyathala, Toni Grell, et al. · Angewandte Chemie (2025) | TGRS Research Map | TGRS