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P,N Ligand in Ni-Catalyzed Cross-Coupling Reactions: A Promising Tool for π-Functionalization

Authors
Bae, JaehanCho, Eun Jin
Issue Date
Oct-2023
Publisher
AMER CHEMICAL SOC
Keywords
nickel; P,N ligands; cross-coupling; alkene; alkyne; pi-functionalization
Citation
ACS CATALYSIS, v.13, no.20, pp 13540 - 13560
Pages
21
Journal Title
ACS CATALYSIS
Volume
13
Number
20
Start Page
13540
End Page
13560
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/68675
DOI
10.1021/acscatal.3c03851
ISSN
2155-5435
Abstract
Bidentate P,N ligands, integrating phosphine and nitrogen donors, are highlighted for their versatile characteristics, offering both electronic and steric tunability. Their hemilabile nature, coupled with the ability to modulate both electronic and steric properties through the choice of donor atoms and substituents, has expanded the horizons of chemical transformations. This Review focuses on Ni-catalyzed cross-coupling reactions mediated by P,N ligands. The asymmetrical nature of P,N ligands, with each donor atom playing a specific role in the catalytic cycle, offers control, stability, and unique regioselectivity in catalytic processes. In particular, the Ni/P,N-catalytic system exhibits remarkable reactivity with pi-substrates including alkenes, alkynes, and allenes. A thorough mechanistic understanding of these processes offers insights into the trends and future directions in Ni/P,N-catalyzed cross-coupling reactions.
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