Multifaceted Hidden Catalysis Revealed by Mechanistic Analysis of FeBr-Catalysed Arene Borylation.

Angew Chem Int Ed Engl

EaStCHEM School of Chemistry, University of Edinburgh, Edinburgh, David Brewster Road. Edinburgh, EH9 3FJ, UK.

Published: December 2024

AI Article Synopsis

  • Arene borylation reactions allow for the creation of aryl organoboranes like boronic esters, typically requiring precious metals for catalysis.
  • Significant research is focused on using Earth-abundant metals; in this case, iron is used with H-B-9-BBN to catalyze reactions without extra ligands.
  • The study reveals that instead of directly catalyzing, the iron salt initiates the production of a more active haloborane, which plays a crucial role in borylation, indicating a new catalytic mechanism in these reactions.

Article Abstract

Arene borylation reactions provide direct access to aryl organoboranes, including aryl boronic esters. Precious metals, namely Ir, Rh, Pt, remain the go-to for metal-catalysed borylation reactions, however, significant efforts have been expended in developing Earth-abundant metal alternatives. The iron-catalysed borylation of 2-aryl pyridine derivatives with 9-borabicyclo[3.3.1]nonane (H-B-9-BBN) offers unique reactivity by using only FeBr as the catalyst, without added ligand(s). Mechanistic analysis of this borylation reaction revealed an alternative, hidden catalysis pathway whereby the iron salt acts not as a borylation catalyst, but as an initiator for the generation of a catalytically active haloborane, Br-B-9-BBN. The roles of iron salt, Br-B-9-BBN, and HBr in catalyst formation, the mode of catalytic turnover, and catalyst regeneration were all determined using single-turnover and catalytic studies. The borylation reaction was found to proceed by a catalytic electrophilic borylation using, in situ generated, Br-B-9-BBN. These studies highlight a new, orthogonal method of generating haloboranes and their previously unobserved role as hidden catalysts within arene borylation reactions.

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http://dx.doi.org/10.1002/anie.202423929DOI Listing

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Multifaceted Hidden Catalysis Revealed by Mechanistic Analysis of FeBr-Catalysed Arene Borylation.

Angew Chem Int Ed Engl

December 2024

EaStCHEM School of Chemistry, University of Edinburgh, Edinburgh, David Brewster Road. Edinburgh, EH9 3FJ, UK.

Article Synopsis
  • Arene borylation reactions allow for the creation of aryl organoboranes like boronic esters, typically requiring precious metals for catalysis.
  • Significant research is focused on using Earth-abundant metals; in this case, iron is used with H-B-9-BBN to catalyze reactions without extra ligands.
  • The study reveals that instead of directly catalyzing, the iron salt initiates the production of a more active haloborane, which plays a crucial role in borylation, indicating a new catalytic mechanism in these reactions.
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