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  • Articles: DFG German National Licenses  (2)
  • 1980-1984  (2)
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  • Articles: DFG German National Licenses  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 2423-2427 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Isocyanide Complexes, III. Organosulfonyl Isocyanide Cr(CO)5 ComplexesThe reaction of K[(CO)5CrCN] with RSO2Cl (R = Me, Et, CH2Ph, Ph, p-MeC6H4 and p-FC6H4) yields the complexes (CO)5CrCNSO2R (3a-f). The compounds are characterized by their IR, NMR, and mass spectra.
    Notes: Bei der Umsetzung von K[(CO)5CrCN] mit RSO2Cl (R = Me, Et, CH2Ph, Ph, p-MeC6H4 und p-FC6H4) entstehen die Komplexe (CO)5CrCNSO2R (3a-f), die anhand ihrer IR-, NMR- und Massenspektren charakterisiert werden.
    Additional Material: 6 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 114 (1981), S. 975-981 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Chalkogenides as Ligands of Complexes, I Carbonyl-Hydrogen Chalkogenide Complexes of Chromium, Molybdenum, and TungstenThe hexacarbonyls of chromium, molybdenum, and tungsten yield the monosubstitution complexes M′[M(CO)5(XH)] (M = Cr, Mo, W;X = S, Se, Te) 1-7 on photochemical or thermal reaction with chalkogenides in alcohols. They are isolated as [(Ph3P)2N]+ - or [AsPh4]+ salts 1a - 7a, respectively. On alkylation of 1a, 4a, and 6a with [Et3O][BF4] the dialkylchalkogenide 1a-7a, respectively. On alkylation of 1a, 4a and 6a with [Et3O] BF4] the dialkylchalkogenide complexes (CO)5Cr(XEt2) (X = S, Se, Te) 8-10 are formed. The preparation of XH-bridged complexes of the type [CO)5M(XH)M(CO)5]-(M = Cr, W;X = S, Se, Te) 11-16 can be accomplished by reacting 1a, 3a-7a with M(CO)5THF. Treatment of 11, 13, and 15 with [Et3O][BF4] leads to loss of a M(CO)5 group and formation of the compounds 8 - 10. The photochemical reaction of Mo(CO)6with Li2S yields [(CO)4Mo(SH)2Mo(CO)42- 17.
    Notes: Die Hexacarbonyle von Chrom, Molybdän und Wolfram bilden bei der photochemischen oder thermischen Umsetzung mit Chalkogenid-Ionen in Alkoholen die monosubstituierten Komplexe M′[M(CO)5(XH)] (M = Cr, Mo, W;X = S, Se, Te) 1-7, die als [(Ph3P)2N] +-bzw. [AsPh4]+-Salze 1a-7a isoliert werden. Die Alkylierung von 1a,4a und 6a mit [Et3O][BF4] führt zu den Dialkylchalkogen-Komplexen (CO)5Cr(XEt2) (X = S, Se, Te) 8-10. Die Darstellung XH-überbrückter Zweikernkomplexe des Typs [CO)5M(XH)M(CO)5]-(M = Cr, W;X = S, Se, Te) 11-16 gelingt durch Umsetzung von 1a und 3a-7a mit M(CO)5THF. Werden die Komplexe 11, 13 und 15 mit [Et3O] [BF4] behandelt, so bilden sich unter Abspaltung eines Metallcarbonylrestes die Verbindungen 8-10. Aus Mo(CO)6 und Li2S erhält man bei der Bestrahlung [(CO)4Mo(SH)2Mo(CO)4]2- 17.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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