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  • Inorganic Chemistry  (2)
  • Analytical Chemistry and Spectroscopy  (1)
Materialart
Erscheinungszeitraum
Schlagwörter
  • 1
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 1111-1118 
    ISSN: 0009-2940
    Schlagwort(e): Aldehyde reactions ; Ruthenium clusters ; Oxidative addition ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Oxidative Addition of Aldehydes and Schiff Bases to Ru3(CO)12Aldehydes show a wide variation of their reactive behaviour towards Ru3(CO)12. Aliphatic and simple aromatic aldehydes form simple oxidative addition products Ru3(CO)10(μ-H)(μ-RC = O) (1) either not at all or in low yields as impure compounds, while under forcing conditions dinuclear ruthenium μ-carboxylate complexes or the hydride H2Ru4(CO)13 are formed. Electron-rich aldehydes give good yields of cluster type 1 (R = p-MeOC6H4, p-Me2NC6H4, ferrocenyl). Schiff bases behave similarly, their oxidative addition products being Ru3(CO)10(μ-H)(μ-RC = NR′) (10, R = C6H5, p-MeOC6H4, p-Me2NC6H4, R′ = C6H5, p-MeC6H4). Of the ortho-substituted benzaldehydes, the methoxy compound produces clusters 6 and 7 resulting from aldehyde oxidative addition and aromatic ortho metalation. Salicylaldehyde and its p-tolylimine give the compounds Ru3(CO)8(μ-η2-OC6H4CH = X)2 (9, 11, X = O, NC6H4Me) with a bridging phenolate and a terminally bound aldehydic O or Schiff base NR function. 3-Pyridinecarbaldehyde reacts quickly with Ru3(CO)12 to give products 8 derived from pyridine CH rather than aldehyde CH oxidative addition. The crystal structures of 9 and 11 were determined.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 355-363 
    ISSN: 0009-2940
    Schlagwort(e): Ruthenium clusters ; Phosphorus ylides ; Oxidative addition ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Three-Centre Oxidative Addition of Phosphorus Ylides to Ru3(CO)12Phosphorus ylides undergo oxidative addition to Ru3(CO)12 to yield a wide range of Ru3 clusters with triply bridging organic ligands derived from the ylides. Ph3P=CH2 forms HRu3(CO)9(μ31-Ph3P  -  CH  -  CO) (1) containing a phosphonio enolate. Ph3P=CH  -  CHO yields a product mixture containing the phosphonio enolate-bridged cluster and its PPh3 derivative 6, the phosphoniomethylidyne-bridged compound H2Ru3(CO)9(μ31-C  -  PPh3) (5), and the ketenylidene-bridged compound H2Ru3(CO)8(PPh3)(μ31-C  -  CO) (7). Thermal treatment converts the phosphonio enolate ligand (in 1) into the phosphoniomethylidyne ligand (in 5), and the latter into the ketenylidene ligand (in 7). With Ph3P=CH  -  C(O)Me and Ru3(CO)12 ortho1-metalated Ru3 derivatives 10, 11 of the phosphonio ketone R3P  -  C  -  C(O)Me are produced, and likewise with Ph3P=CH  -  COOEt the ortho1-metalated derivative 12 of the phosphonio ester R3P  -  C  -  CO2Et. Me3P=CH  -  COOtBu is oxidatively added to form HRu3(CO)9(μ31-Me3P  -  C  -  COOtBu) (13) bearing a phosphonio ester ligand.  -  The crystal structures of 6 and 13 are reported. The sequence of Ru3 clusters and the bonding modes of the μ3 ligands can be related to the surface reactions during Fischer-Tropsch catalysis.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 15 (1984), S. 393-395 
    ISSN: 0377-0486
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The title compounds were prepared and their Raman spectra were measured, assigned and compared with that of PH3GaCl3. The frequencies of the pyramidal GaCl3 unit are sensitive to the basicity of the phosphine ligand. Modes ν(Gap), appreciably coupled to Ph-P stretching vibrations, are located at 316, 260 and 182 cm-1 as medium to weak bands in the spectra of PhPH2GaCl3, Ph2 PHGaCl3 and Ph3PGaCl3, respectively. The P—H stretching and bending modes give rise to medium to strong Raman bands, and these frequencies increase on coordination.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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