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  • 13C NMR  (1)
  • Aminoarsonium ions  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 27 (1989), S. 616-623 
    ISSN: 0749-1581
    Keywords: 13NMR ; Tertiary arsine ; Aminoarsonium ions ; Arsonium ions ; Aminoarsines ; 1H NMR ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C and 1H NMR spectral data for a homologous series of tertiary arsines (R3As, where R = Me, Et, n-Pr and Ph), aminoarsines and arsonium and aminoarsonium salts are reported and discussed. In nearly all cases, quaternization of the tertiary arsine to its corresponding arsonium or aminoarsonium salt causes a decrease in the magnitude of δc. These results are compared with those from an analogous study on the quaternization of tertiary phosphines, R3P. A discussion of the factors that affect the relative magnitudes of δc and R3As and R3P is given. Hammett-Taft dual substituent parameter analysis was used to show that the positive charge on the arsenic in the atomatic quaternary salts is delocalized by an inductive mechanism. The 1H NMR spectra of the n-propyl- and phenyl-containing compounds are non-first order. The δH and nJ(HH) values were determined by iterative computer analysis. Likewise, the nJ(CH) values for the phenyl carbons of [Ph3AsNH2]Cl and [Ph3AsNHMe]Cl were determined from the coupled 13C NMR spectra.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 25 (1987), S. 484-488 
    ISSN: 0749-1581
    Keywords: 1H NMR ; 13C NMR ; 2-Chloro-1,3,2-dioxarsolanes ; Intra- and inter-molecular exchange ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 1H and 13C NMR spectra of solutions of 2-chloro-4,4,5,5-tetramethyl-1,3,2-dioxarsolane (1) and 2-chloro-1,3,2-dioxarsolane (2) are reported as a function of temperature, concentration and solvent. These data indicate rapid intramolecular conformational averaging for (1) and (2) under all the conditions investigated. Additionally, intermolecular conformational averaging processes are shown to be present. The kinetic parameters for intermolecular exchange were obtained from line shape analysis of the 1H NMR data. These results indicate the intermolecular exchange to be bimolecular in nature, involving a four-centered transition state. The O—CH2—CH2-O torsional angle of (2) has been calculated from the analysis of its AA′BB′ 1H NMR spectral patterns, obtained at low concentrations in the absence of intermolecular exchange.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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