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1.
  • Aad, G., et al. (author)
  • 2012
  • swepub:Mat__t (peer-reviewed)
  •  
2.
  • Stokes, F.A., et al. (author)
  • Structure and Bonding of the Manganese(II) Phosphide Complex (t-BuPH(2))(eta(5)-Cp)Mn{mu-(t-BuPH)}(2)Mn(Cp)(t-BuPH(2))
  • 2012
  • In: Organometallics. - : American Chemical Society (ACS). - 0276-7333 .- 1520-6041. ; 31:1, s. 23-26
  • Journal article (peer-reviewed)abstract
    • Rather than achieving bis-deprotonation of the phosphine, reaction of Cp2Mn (Cp = cyclopentadienyl) with t-BuPH2 at room temperature yields monodeprotonation of half of the available phosphine in the product (t-BuPH2)(η5-Cp)Mn{μ-(t-BuPH)}2Mn(Cp)(t-BuPH2) (1). This complex comprises a Mn(II) phosphide and is a dimer in the solid state, containing a Mn2P2 diamond core. Consistent with the observation of a relatively short intermetal distance of 2.8717(4) Å in 1, DFT analysis of the full structure points to a singlet ground state stabilized by a direct Mn–Mn single bond. This is in line with the diamagnetic character of 1 and an 18-electron count at Mn.
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