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  • 1980-1984
  • 1970-1974  (2)
  • Analytical Chemistry and Spectroscopy  (2)
Material
Years
  • 1980-1984
  • 1970-1974  (2)
Year
Keywords
  • Analytical Chemistry and Spectroscopy  (2)
  • Chemistry  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 4 (1972), S. 683-693 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Data for 30 hydrogen bonding pairs taken from the alkanethiols, i-C3H7SH, nC3H9SH and t-C4H9SH, and 16 bases have been obtained by a PMR method. Representative data for i-C3H7SH at 304 ± 2°K are (base, 102K in M-1, -ΔH° in kcal/mole): (CH2)4S, 3·1, 0·8; (CH3)2S, 3·0, 0·9; (CH3)2S2, 3·7, 0·5; (CH3)2CO, 4·7, 0·9; CH3COOC2H5, 5·7, 1·1; (CH2)4O, 6·1, 1·0; HCON(CH3)2, 12, 0·9; (CH3 O)2 SO, 12, 0·9; (C2 H5O)3PO, 6·5, 1·0; CH3 (CH3 O)2PO, 18, 1·0; ((CH3)2N)2 CO, 5·9, 1·1; CH3 CN, 13, 0·6. In essence, the problems and errors involved in obtaining equilibrium data for weak complexes stem from the limited concentration rangethat is accessible. This leads to large uncertainties in the quantities K, ΔH° and ΔS°. Structural effects on hydrogen bonding at the sulfur site, both as Lewis acid or base, are discussed. Two erroneous PMR methods in the literature used for assessing the strength of hydrogen bonds are pointed out.
    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 5 (1973), S. 197-204 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The PMR technique has been used to obtain thermodynamic data for hydrogen bonding of alkanethiols (RSH) in 1:1 dimers in carbon tetrachloride. At ca. 303°K these are (R, 104K(M-1), -ΔH°(kcal/mole), -ΔS°(eu)): n-C3H7, 51 ± 5, 0.9 ± 0.15, 13 ± 1; i-C3H7, 50 ± 10, 0.8 ± 0.3, 13 ± 1; n-C4H9, 35 ± 2, 0.8 ± 0.15, 14 ± 1; t-C4H9, 14 ± 4, 1.1 ± 0.7, 16 ± 2; C6H11, 1.3 ± 2, 0.7 ± 0.3, 15 ± 1. Alkanethiol self-association is weak, and although an exact expression [Eqn. (5)] reproduces spectral data precisely, the fit is sufficiently ‘loose’ or ‘baggy’ so that values of K, ΔH° and ΔS° are uncertain. The methodology of the treatment of self-association data and their errors is examined and Deranleau's useful approach is extended. The impossibility of obtaining reliable data for very weak (〈 10 %) or very strong (〉 90 %) associations by techniques equivalent to ours is emphasized. The possibility of cyclic thiol dimers is discussed. It is suggested that the PMR method cannot give trustworthy self-association data for aryl or arylalkylthiols because of the relatively large anisotropy effects introduced into the dilution shift.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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