4.8 Article

Synthesis of Molecular Phenylcalcium Derivatives: Application to the Formation of Biaryls

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 61, Issue 18, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202200305

Keywords

Aryl Bromides; Biaryls; Calcium; Density Functional Theory; Main Group Chemistry

Funding

  1. EPSRC [EP/R020752/1]
  2. Royal Commission for the Exhibition of 1851

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The synthesis and catalytic properties of hydrocarbon-soluble beta-diketiminato phenylcalcium derivatives are discussed in this article. The compounds display different modes of Ca-mu(2)-Ph-Ca bridging and can selectively and uncatalyzedly form biaryls when reacted with aryl bromides.
Hydrocarbon-soluble beta-diketiminato phenylcalcium derivatives, which display various modes of Ca-mu(2)-Ph-Ca bridging, are accessible from reactions of Ph2Hg and [(BDI)CaH](2). Although the resultant compounds are inert toward the C-H bonds of benzene, they yield selective and uncatalyzed biaryl formation when reacted with readily available aryl bromides.

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