[MoFe3S4]3+ and [MoFe3S4]2+ cubane clusters containing a pentamethylcyclopentadienyl molybdenum moiety

被引:12
|
作者
Komuro, Takashi
Kawaguchi, Hiroyuki
Lang, Jianping
Nagasawa, Takayuki
Tatsumi, Kazuyuki
机构
[1] Nagoya Univ, Grad Sch Sci, Res Ctr Mat Sci, Chikusa Ku, Nagoya, Aichi 4648602, Japan
[2] Nagoya Univ, Grad Sch Sci, Dept Chem, Chikusa Ku, Nagoya, Aichi 4648602, Japan
[3] Inst Mol Sci, Coordinat Chem Labs, Okazaki, Aichi 4448595, Japan
关键词
molybdenum; iron; sulfide; cubane cluster; cyclopentadienyl;
D O I
10.1016/j.jorganchem.2006.07.047
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A series of organometallic molybdenum/iron/sulfur clusters of the general formula [Cp*MoFe3S4Ln](m) (Cp* =eta(5)-C5Me5; L = S'Bu, SPh, Cl, I, n = 3, m = 1-; L-n = I-2(P'Bu-3), m = 0; L = 2,6-diisopropylphenylisocyanide (ArNC), n = 7, m = 1+) have been synthesized. A cubane cluster (PPh4)[Cp*MoFe3S4(S'Bu)(3)] (2) was isolated from a self-assembly reaction of Cp*Mo(S'BU)(3) (1), FeCl3, LiS'Bu, and S-8 followed by cation exchange with PPh4Br in CH3CN, while an analogous cluster (PPh4)[Cp*MoFe3S4(SPh)(3)](3) was obtained from the Cp*MoCl4/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)[Cp*MoFe3S4Cl3] (4), which was in turn converted to (PPh4)[Cp*MoFe3S4I3] (5) by the reaction with NaI. A neutral cubane cluster Cp*MoFe3S4I2(P'Bu-3) (6) was generated upon treating 5 with P'Bu-3. Although reduction of 4 by cobaltocene under the presence of ArNC resulted in a disproportionation of the cubane core to give Fe4S4(ArNC)(9)Cl (7), a similar reduction reaction of 5 produced [Cp*MoFe3S4(ArNC)(7)]I (8), where the MoFe3S4 core was retained. The crystal structures of 4-6, and 8 were determined by the X-ray analysis. (c) 2006 Elsevier B.V. All rights reserved.
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页码:1 / 9
页数:9
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