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Abstract
The synthesis and catalytic properties of Ni(II) complexes with the general formula Ni(NHC)[P(OR)3](Ar)Cl are described. These complexes are air-stable and extremely effective precatalysts in the Suzuki-Miyaura cross-coupling reaction. The reaction protocols described allow for the cross-coupling of aryl chlorides and arylboronic acids, employing low catalytic loading, to deliver a large variety of functionalized biaryl compounds. For the coupling of aryl chlorides with N-heterocyclic boronic acids, TBAF was used as an additive to afford nitrogen-containing biaryl products. Overall, these reaction protocols operate at room or mild temperatures and can be applied to a variety of electronically and sterically differentiated coupling partners. Fundamental insights into the mechanism of this reaction, including the proposed formation of the catalytically active Ni(NHC)[P(Oi-Pr)3] and resting state species, are also reported.
Original language | English |
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Article number | e202504108 |
Number of pages | 11 |
Journal | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION |
DOIs | |
Publication status | E-pub ahead of print - 18 Mar 2025 |
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Dive into the research topics of 'Efficient Nickel Precatalysts for Suzuki-Miyaura Cross-Coupling of Aryl Chlorides and Arylboronic Acids Under Mild Conditions'. Together they form a unique fingerprint.Projects
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Counting the Electrons: Nickel Catalysed Electrochemical C-H Activation
Stewart, S. (Investigator 01), Koutsantonis, G. (Investigator 02) & Dorta, R. (Investigator 03)
ARC Australian Research Council
1/01/23 → 28/02/26
Project: Research