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  • 1
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Metal π-Complexes of Benzene Derivatives, XXIV1). 1H NMR Coordination Shift and Ring Current Quenching in Sandwich Complexes as Studied for Bis(η6-[10]paracyclophane)chromium(0)The title compound was prepared by means of metal atom-ligand vapor cocondensation. Its most conspicuous feature, the well defined disposition of 20 methylene groups in the periphery of the title complex is employed to gauge via 1H NMR the coordination induced quenching of the aromatic ring current in arenes.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Cooperative Effect in π-Ligand-Bridged Binuclear Complexes, VI1). - Cyclopentadienyl-Bridged Binuclear Complexes, Me2Si[(C5H4)M(CO)3]2 (M = W, Mo, Cr) and Me2Si[C5H4)M(CO)3Cl]2 (M = W, Mo): Synthesis and NMR-Spectroscopic CharacteristicsThe cyclopentadienyl-bridged binuclear complexes Me2Si[Cp′M(CO)3]2 (2) (M = W, Mo, Cr) and Me2Si[Cp′M(CO)3Cl]2 (3) (CP′ = C5H4; M = W, Mo) can be prepared by reaction of M(CO)3(EtCN)3 (4) (M = W, Mo, Cr) and Li2(Me2SiCp′2) (7), followed by oxidation with FeCl3 in and aprotic medium. If the oxidation is carried out the presence of proton donors for M = Mo, a mixture of Me2Si[Cp′Mo(CO)3]2 (2b) and [CpMo(CO)3]2 (1b). can be obtained. A complete desilylation is ascertainable after reaction of 4 (M = Mo, Cr) with Me2SiCp2 (5) (Cp = C5H5). for the Cp-bridged complexes the chiral C2 symmetry is proved NMR-spectroscopically at low temperature. This symmetry changes to the averaged achiral C2v symmetry with a barrier of activation ΔGc≠ = 50-70 kJ mol-1. Because of the linkage between the Cp ligands in Me2Si[Cp′Cr(CO)3]2 (2c), a cooperative interaction of the two neighboring Cr centers takes place, impeding the homolysis of the Cr—Cr bond compared to [CpCr(CO)3]2 (1c).
    Notes: Die Cyclopentadienyl-verbrückten Zweikernkomplexe Me2Si[Cp′M(CO)3]2 (2) (M = W, Mo, Cr) und Me2Si[Cp′M(CO)3Cl]2 (3) (CP′ = C5H4; M = W, Mo) werden durch Reaktion von M(CO)3(EtCN)3 (4) (M = W, Mo, Cr) mit Li2(Me2SiCp′2) (7) und anschließende Oxidation mit FeCl3 in aprotischem Medium dargestellt. Sind bei der Oxidation Protonenspender zugegen, findet man für M = Mo ein Produktgemisch aus Me2Si[Cp′Mo(CO)3]2 (2b) und [CpMo(CO)3]2 (1b). Eine vollständige Desilylierung stellt man nach der Umsetzung von 4 mit Me2SiCp2 (5) (Cp = C5H5) für Mo und Cr fest. NMR-spektroskopisch kann für die Cp-verbrückten Komplexe 2 bei tiefen Temperaturen die chirale C2-Symmetrie nachgewiesen werden, die mit einer Aktivierungsschwelle von ΔGc≠ = 50-70 kJ mol-1 in die gemittelte achirale C2-Symmetrie übergeht. Als Folge der Cp-Verbrückung in Me2-Si[Cp′Cr(CO)3]2 (2c) tritt eine kooperative Wechselwirkung zwischen den zwei Cr-Zentren ein, die eine Homolyse der Cr—Cr-Bindung im Vergleich zu [CpCr(CO)3]2 (1c) erschwert.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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