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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 130 (1997), S. 295-298 
    ISSN: 0009-2940
    Keywords: Rhenium ; Oxides ; Alkyl ligands ; Dirhenium compounds ; Metal-metal interactions ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Most alkylrhenium(VII) oxides, e.g. ((cyclo)-C3H5)Re03 (2) are rather sensitive to temperature and moisture with the prominent exception of methyltrioxorhenium (1). The corresponding alkylrhenium(VI) oxides of formula [RR′(O)- Re(μ-O)]2 [R=R′=(cyclo)-C3H5 (3), iPr (4); R=CH3, R′=C2H5 (5), R=CH3, R′=iPr (6)] are much more stable in this regard. They can be handled in air at room temperature. They were synthesized from Re207 and dialkylzinc precursors, fully characterized and are available in much higher yields than their ReVII congeners. Mixed tetraalkyltetraoxodirhenium(VI) complexes (R # R′) synthesized from 1 and dialkylzinc compounds form as a mixture of cis/trans isomers. They are oily liquids at room temperature. The Re=O and Re-Re stretching force constants as a measure of the bond strengths, were determined from IR and Raman data.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0009-2940
    Keywords: N. Ligands ; O ligands ; Rhenium ; Structure elucidation ; Ligand effects ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reaction of [NBu4][ReOCl4] (1) with bidentate salicylidene amine ligands (salen = HL) (2a-c) leads to the formation of monomeric octahedral rhenium (V) compounds of formula [ReOCl (L)2] (3a-c). Spectroscopic date indicate asymmetric arrangement of the ligands in the complexes. This is confirmed by the X-ray crystal structures of 3b and 3c. Complexes 3a, b have been tested as catalysts for the epoxidation of cyclooctene. No evidence for decomposition for decomposition of the catalysts is observed during the reaction (as in the case for tri-and tetra-dentate salen complexes). No undesired byproducts are formed in the catalytic reactions.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1434-1948
    Keywords: Chromium ; Carboxylate complexes ; Metal-metal multiple bonds ; Molybdenum ; Rhenium ; Tungsten ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reaction of Re2{μ-O2CC(CH3)3}4Cl2 with [(CO)5M-CN]Na (M = Cr, Mo, W) leads to tetranuclear complexes of formula Re2{μ-O2CC(CH3)3}4[-NC-M(CO)5]2 (M = Cr, Mo, W). These complexes were characterized by 1H-, 13C-, and 95Mo-NMR, IR and Raman spectroscopy, elemental analysis and examined by cyclic voltammetry. The applied methods show the donor capabilities of the [(CO)5M-CN]- ligands which shift electron density towards the Re centers weakening the Re-Re quadruple bond. The Re-Re bond lengths and the ν(Re-Re) force constants are estimated based on the FT-IR and Raman examinations. Photochemical examinations and TG/MS experiments have also been conducted. The latter method shows that the product complexes decompose around 100 °C, by first loosing their carbonyl substituents; as do the Cr, Mo, W precursor compounds. The dirhenium tetrapivalate unit decomposes only at higher temperatures in a distinct second step.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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