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Catalytic C-F Bond Activation of Perfluoroarenes by Tricoordinated Gold(I) Complexes

Journal

ADVANCED SYNTHESIS & CATALYSIS
Volume 354, Issue 8, Pages 1529-1541

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.201100843

Keywords

catalysis; C?F bond activation; DFT calculations; gold complexes; hydrodefluorination

Funding

  1. National Key Basic Research Support Foundation of China (NKBRSFC) [2010CB912302]
  2. National Scientific Foundation of China [20971007]

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We report the first example of gold catalyzing C?F bond activation for perfluoroarenes in the presence of silanes. Tricoordinated gold(I) complexes supported by Xantphos-type ligands, such as Xantphos and tBuXantphos ligands, exhibit efficacy in the hydrodefluorination (HDF) of various types of perfluoroarenes. For [tBuXantphosAu(AuCl2)], the highest turnover number is up to 1000 in the HDF of pentafluoronitrobenzene with diphenylsilane. An examination of functional group tolerance shows the orthogonality of this gold(I) catalytic protocol to ketone, ester, carboxylate, alkynyl, alkenyl and amide groups, suggesting its potential application in chemoselective C?F activations. Mechanistic studies show that the equilibrium between tetracoordinated [L2Au]+ and [LAu]+ is important for the reactivity of gold catalysts, which is dependent on the sterically bulky group of Xantphos-type ligands. Furthermore, computational studies for the possible reaction pathways suggest that direct oxidative addition of C?F bonds by gold(I) cation might be the key step during these catalytic reactions.

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