Naked (C5Me5)2M Cations (M = Sc, Ti, and V) and Their Fluoroarene Complexes
datasetposted on 19.10.2005, 00:00 by Marco W. Bouwkamp, Peter H. M. Budzelaar, Jeroen Gercama, Isabel Del Hierro Morales, Jeanette de Wolf, Auke Meetsma, Sergei I. Troyanov, Jan H. Teuben, Bart Hessen
The ionic metallocene complexes [Cp*2M][BPh4] (Cp* = C5Me5) of the trivalent 3d metals Sc, Ti, and V were synthesized and structurally characterized. For M = Sc, the anion interacts weakly with the metal center through one of the phenyl groups, but for M = Ti and V, the cations are naked. They each contain one strongly distorted Cp* ligand, with one (V) or two (Ti) agostic C−H···M interactions involving the Cp*Me groups. For Sc and Ti, these Lewis acidic species react with fluorobenzene and 1,2-difluorobenzene to yield [Cp*2M(κF-FC6H5)n][BPh4] (M = Sc, n = 2; M = Ti, n = 1) and [Cp*2M(κ2F-1,2-F2C6H4)][BPh4], the first examples of κF-fluorobenzene and κ2F-1,2-difluorobenzene adducts of transition metals. With the perfluorinated anion [B(C6F5)4]-, both Sc and Ti form [Cp*2M(κ2F-C6F5)B(C6F5)3] contact ion pairs. The nature of the metal−fluoroarene interaction was studied by density functional theory (DFT) calculations and by comparison with the corresponding tetrahydrofuran (THF) adducts and was found to be predominantly electrostatic for all metals studied.