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  • 1-Alken-3-ynes  (1)
  • Molybdenum  (1)
  • 1
    ISSN: 0009-2940
    Schlagwort(e): 1-Alken-3-ynes ; Manganese(III) acetate ; Propargyl radical ; Ligand-transfer reaction ; Electron-transfer reaction ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Control of the Propargylic Radical Stabilization by Carbon-Chain Length in Manganese(III)-Mediated Reactions of 1-Alken-3-ynes. - A Facile Synthetic Way to Long-Chain 4-Acetoxy-5-alkynoic AcidsBy investigation of reactions of 1-alken-3-ynes RC ≡ C - CH = CH2 4 with acetic acid/acetic anhydride, mediated by manganese(III) acetate, it has been found that the stabilization of propargylic radical adducts depends on the carbon-chain length of R in 4. R = C8H17 is shown to be the “critical” chain length when ligand transfer reaction appears to be the only way of stabilization of intermediates, thus providing a facile one-step access to long-chain 4-acetoxy-5-alkynoic acids. The dependence of the product ratios on the AcOH/Ac2O ratio has also been demonstrated.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 1434-1948
    Schlagwort(e): Radicals ; Carbenium ions ; Clusters ; Cobalt ; Molybdenum ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Complexed α-CF3 propargyl alcohols of the general formula [(M2L6){μ-η2,η2-RC≡CCH(CF3)(OH)}] were prepared with M2L6 = Co2(CO)6, R = CH3(CH2)4- (1), R = C6H5- (2); M2L6 = Co2(CO)5P(C6H5)3, R = CH3(CH2)4- (3a,b), R = C6H5- (4a,b); M2L6 = Co2(CO)4dppm, R = C6H5- (5); M2L6 = Co(CO)3MoCp(CO)2, R = CH3(CH2)4- (6a,b), R = C6H5- (7a,b). An X-ray molecular structure of the propargyl-alcohol complex [{Co2(CO)4dppm}{μ-η2,η2-C6H5C≡CCH(CF3)(OH)}] (5) was also determined. The related carbenium ions [(M2L6){μ-η2,η3-RC≡CCH(CF3)}][BF4] (8-12) were obtained from the parent propargyl alcohol complexes by direct protonation with HBF4· Et2O in diethyl ether. These carbenium ions were reduced further by Zn in CH2Cl2 to give the alkyne adducts [(M2L6){μ-η2,η2-RC≡CCH2(CF3)}] (13-17), as confirmed by the X-ray molecular structure of [(Co2(CO)4dppm){μ-η2,η2-C6H5C≡CCH2(CF3)}] (17). Treatment of the carbenium ion complex [{Co(CO)3MoCp(CO)2}{μ-η2,η3-CH3(CH2)4C≡CCH(CF3)}][BF4] (8) with NaSMe unexpectedly afforded the reduced alkyne adduct [{Co(CO)3MoCp(CO)2}{μ-η2,η2-CH3(CH2)4C≡CCH2(CF3)}] (13), along with the alkyne-thioether diastereomers {Co(CO)3MoCp(CO)2}{μ-η2,η2-CH3(CH2)4C≡CCH(CF3)[(SMe)}] (18a,b). Presumably, all the reduction reactions proceed primarily by the formation of the transient radical species, which are subsequently transformed into the reduced alkyne complexes by hydrogen abstraction from the solvent medium. Interestingly, in the case of the complexed alcohols [{Co2(CO)5P(C6H5)3}{μ-η2,η2-RC≡CCH(CF3)(OH)}] (3a,b) and (4a,b), the reduction process occurs in acidic medium in THF/CH2Cl2. An extensive study of the electronic and steric factors that influence the stability and reactivity of the carbenium ions were performed, which allowed us to explain the behavior of the related radical species in solution during the reduction process.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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