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Heterokuban‐Cluster‐Verbindungen (NEt4){Y=M[(μ3‐S)Re(CO)3]3(μ3‐E)} (M = W oder Mo,Y = O oder S,E = S oder Se): Strukturen,Spektroskopie und Elektrochemie
Authors:Fridmann Hornung  Matthias Wanner  Karl Wilhelm Klinkhammer  Wolfgang Kaim  Jan Fiedler
Abstract:Heterocubane Cluster Compounds (NEt4){Y=M(μ3‐S)Re(CO)3]33‐E)} (M = W or Mo, Y = O or S, E = S or Se): Structures, Spectroscopy, and Electrochemistry Thiometallates MS4]2– (M = Mo, W) or WOS3]2– react with Re(CO)5(O3SCF3) and Li2E (E = S or Se) to yield the following compounds which were structurally characterized: (NEt4){S=W(μ3‐S)Re(CO)3]33‐S)}(NEt4) ( 1 ), (NEt4){O/S=W(μ3‐S)Re(CO)3](μ3‐S)}(NEt4) ( 1 / 2 ), (mixed crystals), (NEt4){S=W(μ3‐S)Re(CO)3]33‐Se)}(NEt4) ( 3 ) and (NEt4){S=Mo(μ3‐S)Re(CO)3]33‐S)}(NEt4) ( 4 ). The heterocubane anions 1 – 4 contain electron‐rich centers such as rhenium(I) or sulfide whereas molybdenum(VI) or tungsten(VI) act as acceptor sites. Accordingly, the absorption spectra show long‐wavelength metal‐to‐ligand charge transfer transitions, and cyclic voltammetry reveals a quasi‐reversible reduction of the clusters. Although both six‐coordinate rhenium(I) and four‐coordinate metal(VI) centers are present in the clusters there is no evidence for significant metal‐to‐metal charge transfer interaction.
Keywords:Cluster compounds  Crystal structures  Rhenium compounds  Sulfide ligand  Thiometallates
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