Homoleptic permethylpentalene complexes: "double metallocenes" of the first-row transition metals.

Journal article

The synthesis of the bimetallic permethylpentalene complexes Pn*2M2 (M = V, Cr, Mn, Co, Ni; Pn* = C8Me6) has been accomplished, and all of the complexes have been structurally characterized in the solid state by single-crystal X-ray diffraction. Pn*2V2 (1) and Pn*2Mn2 (3) show very short intermetallic distances that are consistent with metal-metal bonding, while the cobalt centers in Pn*2Co2 (4) exhibit differential bonding to each side of the Pn* ligand that is consistent with an eta(5):eta(3) formulation. The Pn* ligands in Pn*2Ni2 (5) are best described as eta(3):eta(3)-bonded to the metal centers. (1)H NMR studies indicate that all of the Pn*2M2 species exhibit D(2h) molecular symmetry in the solution phase; the temperature variation of the chemical shifts for the resonances of Pn*2Cr2 (2) indicates that the molecule has an S = 0 ground state and a thermally populated S = 1 excited state and can be successfully modeled using a Boltzmann distribution (DeltaH(o) = 14.9 kJ mol(-1) and DeltaS(o) = 26.5 J K(-1) mol(-1)). The solid-state molar magnetic susceptibility of 3 obeys the Curie-Weiss law with mu(eff) = 2.78 muB and theta = -1.0 K; the complex is best described as having an S = 1 electronic ground state over the temperature range 4-300 K. Paradoxically, attempts to isolate the "double ferrocene" equivalent, Pn*2Fe2, led only to the isolation of the permethylpentalene dimer Pn*2 (6). Solution electrochemical studies were performed on all of the organometallic compounds; 2-5 exhibit multiple quasi-reversible redox processes. Density functional theory calculations were performed on this series of complexes in order to rationalize the observed structural and spectroscopic data and provide estimates of the M-M bond orders.

Authors: Ashley, A; Cooper, RT; Wildgoose, G; Green, J; O'Hare, D

• Publication status: Published
• Journal: Journal of the American Chemical Society
• Volume: 130
• Issue: 46
• Pages: 15662-15677
• Publication date: 2008-11-01
• DOI: 10.1021/ja8057138
• EISSN: 1520-5126
• ISSN: 0002-7863
• Language: English