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A well-defined terminal vanadium(III) oxo complex

  • Author(s): King, AE
  • Nippe, M
  • Atanasov, M
  • Chantarojsiri, T
  • Wray, CA
  • Bill, E
  • Neese, F
  • Long, JR
  • Chang, CJ
  • et al.

Published Web Location

https://doi.org/10.1021/ic5010177
Abstract

© 2014 American Chemical Society. The ubiquity of vanadium oxo complexes in the V+ and IV+ oxidation states has contributed to a comprehensive understanding of their electronic structure and reactivity. However, despite being predicted to be stable by ligand-field theory, the isolation and characterization of a well-defined terminal mononuclear vanadium(III) oxo complex has remained elusive. We present the synthesis and characterization of a unique terminal mononuclear vanadium(III) oxo species supported by the pentadentate polypyridyl ligand 2,6-bis[1,1-bis(2-pyridyl)ethyl]pyridine (PY5Me2). Exposure of [VII(NCCH3)(PY5Me2)]2+(1) to either dioxygen or selected O-atom-transfer reagents yields [VIV(O)(PY5Me2)]2+(2). The metal-centered one-electron reduction of this vanadium(IV) oxo complex furnishes a stable, diamagnetic [VIII(O)(PY5Me2)]+(3) species. The vanadium(III) oxo species is unreactive toward H- and O-atom transfer but readily reacts with protons to form a putative vanadium hydroxo complex. Computational results predict that further one-electron reduction of the vanadium(III) oxo species will result in ligand-based reduction, even though pyridine is generally considered to be a poor π-accepting ligand. These results have implications for future efforts toward low-valent vanadyl chemistry, particularly with regard to the isolation and study of formal vanadium(II) oxo species.

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