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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 33 (1995), S. 553-556 
    ISSN: 0749-1581
    Keywords: NMR ; 13C NMR ; 31P NMR ; 1,4-dihydro-1λ5,4λ5-diphosphinines ; ABX spin systems ; sign of 2J(PC),4J(PC) coupling constants ; isotope effects ; 3J(PP) ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The ABX spin systems of the [mono-13C]isotopomers with vinylic and phenyl ipso-13C atoms of a number of symmetrical 1,4-dihydro-1,4-diphenyl-1λ5,4λ5-diphosphinines were analysed. The substituent dependence of the absolute signs and magnitudes of 2J(PC) between the two 31P nuclei and two vinylic 13C atoms and of the 4J(PC) and 3J(PP) are reported. 13C isotope effects on δ(31P) and 3J(PP) are discussed.
    Additional Material: 1 Ill.
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  • 2
    ISSN: 0044-2313
    Keywords: 1,′,3,3′-Tetrakis(dimethylamino)-1λ5, 3λ5-diphosphete ; sulfanolysis ; bis(dimethylamino)thiophos-phonylmethylidene-methyl-bis(dimethylamino)phosphorane ; 1,′, 3,3′ -tetrakis(dimethylamino)-2,4-bis-(ethylthio)-1λ5, 3λ5-diphosphete ; 1,′,3,3′-tetrakis(dimethyl-amino)-1,2-dihydro-3λ5-[1,3]-diphosphetiumthiophenolate ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reaction of 1,′, 3,3′-Tetrakis(dimethylamino)-1λ5,3λ5-diphosphete with S—H Acidic Compounds.Reaction of 1,′,3,3′-tetrakis(dimethyl-amino)-1λ5,3λ5-diphosphete (1) with hydrogen sulfide yields bis(dimethylamino)thiophosphonylmethylidene-methyl-bis(dimethylamino)phosphorane (5).Water eliminates dimethylamine from 5 and forms bis(dimethyl-amino)thiophosphonyl-methyl(dimethylamino)phosphonylmethylene 6. The reaction of 1 with ethylmercaptane yields the 2,4-bis(ethylthio)-derivative of 1, i.e. compound 8 and bis(dimethylamino)phosphanylmethylidene-methyl-bis(dimethylamino)phosphorane (9), which is also formed from 1 and 2,4,6-trimethylphenylphosphane. Thiophenol protonates 1 to give the corresponding cation which is isolated as its thiophenolate, 10. Properties, nmr and mass spectra of 5, 6 and 8 - 10 are described and discussed.
    Notes: Die Reaktion von 1,′,3,3′-Tetrakis(dimethylamino)-1λ5, 3λ5 -diphosphet (1) mit Schwefelwasserstoff führt zu Bis(dimethylamino)thiophosphonylmethyliden-methyl-bis(dimethylamino)phosphoran(5). Wasser spaltet aus 5 Dimethylamin ab und bildet Bis(dimethylamino)thiophosphonyl-methyl(dimethylamino)phosphonylmethylen 6. Bei der Umsetzung von 1 mit Ethylmercaptan entstehen das 2,4-Bis(ethylthio)-Derivat von 1, die Verbindung 8 und Bis(dimethylamino)-phosphanylmethyliden-methyl-bis(dimethylamino)phosphoran (9), das auch aus 1 und 2, 4, 6-Trimethylphenyl-phosphan gebildet wird. Thiophenol protoniert 1 zum entsprechenden Kation, das als Thiophenolat 10 isoliert wird. Eigenschaften, NMR- und Massenspektren von 5, 6 und 8 - 10 werden beschrieben und diskutiert.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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