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[MoFe3S4]3+ and [MoFe3S4]2+ cubane clusters containing a pentamethylcyclopentadienyl molybdenum moiety
Institution:1. Research Center for Materials Science, and Department of Chemistry, Graduate School of Science, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8602, Japan;2. Coordination Chemistry Laboratories, Institute for Molecular Science, Myodaiji, Okazaki 444-8595, Japan
Abstract:A series of organometallic molybdenum/iron/sulfur clusters of the general formula Cp1MoFe3S4Ln]m (Cp1 = η5-C5Me5; L = StBu, SPh, Cl, I, n = 3, m = 1−; Ln = I2(PtBu3), m = 0; L = 2,6-diisopropylphenylisocyanide (ArNC), n = 7, m = 1+) have been synthesized. A cubane cluster (PPh4)Cp1MoFe3S4(StBu)3] (2) was isolated from a self-assembly reaction of Cp1Mo(StBu)3 (1), FeCl3, LiStBu, and S8 followed by cation exchange with PPh4Br in CH3CN, while an analogous cluster (PPh4)Cp1MoFe3S4(SPh)3] (3) was obtained from the Cp1MoCl4/FeCl3/LiSPh/PPh4Br reaction system or from a ligand substitution reaction of 2 with PhSH. Treatment of 2 with benzoyl chloride gave rise to (PPh4)Cp1MoFe3S4Cl3] (4), which was in turn converted to (PPh4)Cp1MoFe3S4I3] (5) by the reaction with NaI. A neutral cubane cluster Cp1MoFe3S4I2(PtBu3) (6) was generated upon treating 5 with PtBu3. Although reduction of 4 by cobaltocene under the presence of ArNC resulted in a disproportionation of the cubane core to give Fe4S4(ArNC)9Cl (7), a similar reduction reaction of 5 produced Cp1MoFe3S4(ArNC)7]I (8), where the MoFe3S4 core was retained. The crystal structures of 46, and 8 were determined by the X-ray analysis.
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