4.7 Article

Cyclometallation of arylimines and nitrogen-containing heterocycles via room-temperature C-H bond activation with arene ruthenium(II) acetate complexes

Journal

DALTON TRANSACTIONS
Volume 41, Issue 36, Pages 10934-10937

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2dt31401k

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Funding

  1. CNRS
  2. French Ministry for Research
  3. Institut Universitaire de France
  4. ANR program [09-Blanc-0101-01]
  5. Chinese Scholarship Council

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The reaction of [RuCl2(p-cymene)](2) with arylimines and 4 equiv. of KOAc in methanol at room temperature produces stable ((NC)-C-boolean AND)-cyclometallated ruthenium(II) complexes via C-H bond activation/deprotonation. This method can be applied also to nitrogen-containing molecules: N-phenylpyrazole, 2-phenyl-2-oxazoline and benzo[h]quinoline. N-Phenylpyrazole, [RuCl2(p-cymene)](2) and diphenylacetylene directly lead to alkyne insertion into the metallacycle C-Ru bond.

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