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Stannylenes and Germylenes Stabilized by Tetradentate Bis(amidine) Ligands with a Rigid Naphthalene Backbone.

Alejandra AcuñaSonia Mallet-LadeiraJean-Marc SotiropoulosEddy MaertenAlan R CabreraAntoine BaceiredoTsuyoshi KatoRené Segundo Rojas GuerreroDavid Madec
Published in: Molecules (Basel, Switzerland) (2024)
An unusual series of germylenes and stannylenes stabilized by new tetradentate bis(amidine) ligands RNC(R')N-linker-NC(R')NR with a rigid naphthalene backbone has been prepared by protonolysis reaction of Lappert's metallylenes [M(HMDS) 2 ] (M = Ge or Sn). Germylenes and stannylenes were fully characterized by NMR spectroscopy and X-ray diffraction analysis. DFT calculations have been performed to clarify the structural and electronic properties associated with tetradentate bis(amidine) ligands. Stannylene L 1 Sn shows reactivity through oxidation, oxidative addition, and transmetalation reactions, affording the corresponding gallium and aluminum derivatives.
Keyphrases
  • ionic liquid
  • density functional theory
  • high resolution
  • molecular dynamics
  • molecular dynamics simulations
  • hydrogen peroxide
  • molecular docking
  • electron microscopy
  • magnetic resonance imaging
  • magnetic resonance