4.8 Article

Base Metal Catalysts for Photochemical C-H Borylation That Utilize Metal-Metal Cooperativity

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 135, Issue 46, Pages 17258-17261

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja408861p

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Funding

  1. UIC Department of Chemistry
  2. UIC Campus Research Board

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Heterobimetallic Cu-Fe and Zn-Fe complexes catalyze C-H borylation, a transformation that previously required noble metal catalysts. The optimal catalyst, (IPr)Cu-FeCp(CO)(2), exhibits efficient activity at 5 mol% loading under photochemical conditions, shows only minimal decrease in activity upon reuse, and is able to catalyze borylation of a variety of arene substrates. Stoichiometric reactivity studies are consistent with a proposed mechanism that exploits metal-metal cooperativity and showcases bimetallic versions of the classical organometallic processes, oxidative addition and reductive elimination.

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