4.8 Article

Co(III) Imidos Exhibiting Spin Crossover and C-H Bond Activation

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 134, Issue 43, Pages 17858-17861

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja307699u

Keywords

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Funding

  1. Harvard University
  2. NSF [CHE-0955885, NSF/CHE-0822838]
  3. William Lipscomb Memorial Fund
  4. G.T.S. the NSF
  5. George W. Merck Fellowship
  6. DOE [DE-AC02-06CH11357]
  7. Direct For Mathematical & Physical Scien
  8. Division Of Chemistry [0822838] Funding Source: National Science Foundation
  9. Division Of Chemistry
  10. Direct For Mathematical & Physical Scien [0955885] Funding Source: National Science Foundation

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The reaction of (L-Ar)Co(py) with (BuN3)-Bu-t afforded the isolable three-coordinate Co-imido complex (L-Ar)Co((NBu)-Bu-t), which is paramagnetic at room temperature. Variable-temperature (VT) H-1 NMR spectroscopy, VT crystallography, and magnetic susceptibility measurements revealed that (L-Ar)Co((NBu)-Bu-t) undergoes a thermally induced spin crossover from an S = 0 ground state to a quintet (S = 2) state. The reaction of (L-Ar)Co(py) with mesityl azide yielded an isolable S = 1 terminal imido complex that was converted into the metallacycloindoline (L-Ar)Co(kappa(2)-NHC6H2-2,4-Me-2-6-CH2) via benzylic C-H activation.

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