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  • 1
    ISSN: 1572-8862
    Keywords: polyoxoalkoxometalate ; iron cluster ; mixed iron–vanadium cluster ; hexametalate core ; decametalate core
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract Solvatothermal syntheses have been exploited to effect the isolation of three novel polyoxoalkoxometalate clusters, [{Fe(OH)(CH3CN)2} Fe6OCl6{(OCH2)3CCH2OH}4] (1), [Fe10O2Cl8{(OCH2)3CCH2CH3}6] (2), and [(VO)2Fe8O2Cl6{(OCH2)3CCH2CH3}6] (3). The structure of 1 may be described as a hexametalate core {Fe6OCl6}10+, consisting of a octahedral arrangement of chloride ligands encasing an octahedron of six Fe(III) sites, with a central oxo group. The remaining four coordination sites at each octahedral iron center are occupied by doubly bridging oxygen donors from the trisalkoxo ligands. One triangular face of this substructure, defined by three oxygen atoms, from three adjacent trisalkoxo ligands, is capped by the {Fe(OH)(CH3CN)2}2+ subunit. The structure of 2 is based on the decametalate core of edge-sharing octahedra. The eight peripheral Fe(III) sites of the cluster bond to four oxygen donors from the trisalkoxo ligands, a terminal Cl− ligand, and one of the μ 6-oxo groups. The two central iron sites are linked to four oxygen donors from the trisalkoxo ligands and to both of the μ 6-oxo groups. Cluster 3 is structurally related to 2 with two {FeCl}2+ units replaced by {VO}2+ groups.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Molecular engineering 3 (1993), S. 93-120 
    ISSN: 1572-8951
    Keywords: Polyoxoalkoxymetalates ; polyoxovanadates ; polyoxomolybdates ; metal alkoxides ; clusters ; tetrametalate core ; hexametalate core ; decametalate core ; hydrothermal synthesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract While the chemistry of polyoxoanions has been extensively studied, the related polyoxoalkoxide clusters remain relatively unexplored. Recent investigations into the coordination chemistry of polyoxoanions with alkoxide ligands demonstrate the existence of a rich structural chemistry which is now emerging. The introduction of alkoxide ligands into polyoxoanion cores significantly expands the structural diversity of the cluster types and allows the isolation not only of fully-oxidized cores with all metal centers possessing d0 electronic configurations but of fully-reduced and mixed valence systems.
    Type of Medium: Electronic Resource
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