The ligand‐unsupported accommodation of extra metal moieties in a sandwich complex is reported. Although it has been considered that the metal‐capacity of a metal sheet sandwich complex is strictly limited by the size of cyclic unsaturated hydrocarbon ligands, the M−M edge bonds in a metal sheet sandwich complex provide a ligand‐unsupported docking site for extra metal moieties, allowing expansion of metal‐capacity in sandwich complexes. The metal sheet sandwich complex [Pd4(μ4‐C8H8)(μ4‐C9H9)]+, in which the ligand‐based metal capacity is full in terms of the usage of all C=C moieties of the smaller carbocyclic ligand C8H8 in coordination, can accommodate extra M0{P(OPh)3}2 (M=Pd, Pt) moieties without coordinative assistance by either the C9H9 or the C8H8 ligand.
The ligand‐unsupported accommodation of extra metal moieties in a sandwich complex is reported. Although it has been considered that the metal‐capacity of a metal sheet sandwich complex is strictly limited by the size of cyclic unsaturated hydrocarbon ligands, the M−M edge bonds in a metal sheet sandwich complex provide a ligand‐unsupported docking site for extra metal moieties, allowing expansion of metal‐capacity in sandwich complexes. The metal sheet sandwich complex [Pd4(μ4‐C8H8)(μ4‐C9H9)]+, in which the ligand‐based metal capacity is full in terms of the usage of all C=C moieties of the smaller carbocyclic ligand C8H8 in coordination, can accommodate extra M0{P(OPh)3}2 (M=Pd, Pt) moieties without coordinative assistance by either the C9H9 or the C8H8 ligand.
011ChemInform Abstract Gas-phase acidities are determined for HRe(CO)5, HMn(CO)3(PF3)2, HMn(CO)2(PF3)3, HCo(PF3)4, HIr(PF3)4 and HMn(CO)5. The most striking result is that all reference anions react with HCo(PF3)4, establishing HCo(PF3)4 as the strongest gas-phase acid known to date. The comparison of the acidities of the PF3-substituted manganese complexes to that of HMn(CO)5 reveals that even partial substitution of PF3 for CO dramatically increases the acidity of the hydride.
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