Nickel-Catalyzed Cross-Coupling of Aromatic Ethers

  • Author: Angewandte Chemie International Edition
  • Published Date: 20 October 2021
  • Copyright: Wiley-VCH GmbH
thumbnail image: Nickel-Catalyzed Cross-Coupling of Aromatic Ethers

Metal catalysts are widely used in the production of drugs, dyes, adhesives, and plastics. Andryj M. Borys and Eva Hevia, University of Bern, Switzerland, have discovered an intriguing property of nickel as a catalyst: It can catalyze the coupling of aromatic hydrocarbons in its anionic form, i.e., as a nickelate ion. In this form, two metals, lithium and nickel, work in cooperation in a unique manner.

Cross-Coupling Reactions

Carbon-based structures are usually constructed using palladium catalysts. One of the most widespread reactions for producing these structures is cross-coupling, in which two hydrocarbon fragments are joined together to create a more complex entity. However, some substrates cannot successfully participate in the reaction, meaning chemists have to find alternative routes or activate the substrate to make it compatible with these coupling reactions.

In some of these scenarios, nickel could be used as an earth-abundant alternative catalyst. The team demonstrated that nickel can form negatively charged intermediates under certain conditions. These intermediates can be used to promote reactions in substrates that are otherwise tricky to work with.

For example, a nickel catalyst can catalyze the cross-coupling of aryl ethers, substances found in tar and other crude-oil products that form the basis of a number of specialty chemicals. These substances have very limited reactivity and usually have to be laboriously activated by chemists before they can be used. The researchers investigated the reaction of phenyllithium, an activated benzol, with β-naphthol methyl ether, a basic aryl ether, using the nickel catalyst Ni(COD)2.

Anionic Pathway

The team discovered that a nickelate ion was formed in the very first reaction step. Two molecules of phenyllithium transferred their negatively charged phenyl radical to the neutral nickel atom. According to the researchers, this was only possible because the structure of the nickelate intermediate was stabilized both by the positively charged lithium ions and by coordinated solvent molecules.

As the reaction progressed, the nickelate catalyst initiated the cleavage of the challenging carbon–oxygen bond in the ether substrate and its coupling with one of the phenyl fragments, thus, making it possible for the phenylnaphthalene product to form. The reaction was heavily dependent on the solvent used, and the cooperation between lithium and nickel was key for its success.

This anionic reaction pathway offers an appealing alternative to standard palladium-catalyzed cross-couplings. The team's work has revealed its dependence on the formation and the stability of the catalyst used. "The mechanistic insights gained through this study should allow for further developments in the applications of nickel catalysis in sustainable synthesis," Hevia says.



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