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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 27 (1992), S. 1114-1120 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A mass spectrometric study of eight new carbohydrate derivatives has been carried out to determine the influence of structure on the fragmentation mechanisms of stereoisomers. Results indicate that the relative intensities of peaks due to fragment ions of each pair of isomers are sometimes very different, especially those observed in the collision-induced decomposition mass spectra of [MH]+ ions. Metastable decompositions related to identical fragmentation processes of two isomers release different amounts of kinetic energy, however. It is usually observed that the kinetic energy released is larger for the S-configuration than for the R-configuration of the two epimers of a particular species.
    Additional Material: 6 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 28 (1993), S. 1229-1237 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The breakdown diagrams and photoionization efficiency curves of isomeric chlorobutane ions were obtained by energy-selected molecular ions with the photoelectron-photoion coincidence (PEPICO) technique. The loss of HCl from 1- and 2-chlorobutane molecular ions was found to be fast, and accurate dissociation onsets were determined from the crossover energy in the breakdown diagrams and appropriately corrected for the precursor thermal energy. In spit of the low activation energy, the isochlorobutane molecular ion was found to dissociate slowly near the dissociation limit, the time-of-flight distribution having been analyzed in terms of two exponential decay rates. The dissociation reaction involved a large kinetic energy release that pointed to a 1,2-elimination leading to a stable C4H8+· ion. AB initio calculations indicated that the reaction path involved an H-atom transfer through a barrier, which is a favorable case for a tunneling model to explain the slow decomposition rate. The kinetic energy release of chlorine radical loss from tert-chlorobutane was determined as a function of the ion internal energy. At low energies the kinetic energy release was nearly statistical but the dissociation from the excited electronic states resulted in a large and non-statistical kinetic energy release.
    Additional Material: 9 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 16 (1988), S. 399-402 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A mass spectrometric study of six new α-methylene-γ-lactone carbohydrate derivatives has been carried out in order to correlate the occurrence of metastable transitions with the stereochemistry of the compounds. Results indicate that the decomposition of some metastable fragment ions usually releases higher amounts of kinetic energy when the chiral centre of the lactone ring has the (S) configuration. However, the kinetic energy released on the decomposition of metastable molecular ions seems to follow different trends as regards the configuration of the chiral centre of the lactone moiety, when one or two isopropylidene rings are present in the molecule. This study is being extended to some related compounds in order to confirm whether the kinetic energy release is preferentially affected in a particular way by the chirality.
    Additional Material: 1 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 18 (1995), S. 692-694 
    ISSN: 0935-6304
    Keywords: Capillary gas chromatography ; Intestinal permeability ; Urine ; Sugars ; Lactulose ; Mannitol ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Alteration of intestinal permeability towards compounds like sugars is an indication of abnormalities observed in some diseases. Measurement of the dual sugar absorption of lactulose and mannitol is a non-invasive test of intestinal permeability. The use of this test is however limited by difficulties in the analysis of sugars in urine at low concentrations. In this study we have developed an analytical procedure for quantitative assay of the lactulose-mannitol pair in urine by high resolution gas chromatography. The minimum detectable amounts are 7.5 pg for lactulose and 4.4 pg for mannitol. The calibration curves are linear in the range of 100-6400 mg L-1. Recoveries are within the range 86-102 % for mannitol and 84-105 % for lactulose.
    Additional Material: 4 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 19 (1996), S. 180-182 
    ISSN: 0935-6304
    Keywords: trans-Fatty acids ; Semi-industrial frying ; Capillary GC ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 19 (1996), S. 207-212 
    ISSN: 0935-6304
    Keywords: Capillary gas chromatography ; Headspace ; Phenols ; Derivatization ; Soils ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A quick, simple and selective procedure has been developed for the determination of phenol, o-cresol, m-cresol, and p-cresol in soil samples. The method is based on the gas chromatographic headspace analysis of phenols as acetate derivatives. These acetates were prepared directly in the wetted soil samples by acetic anhydride in the presence of KHCO3· With this procedure sample handling is reduced to a minimum as desorption and derivatization of the analytes are developed from the wetted samples inside the vial of the head space sampler.The acetate esters were analyzed using a 60 m × 0.56 mm DIIDP capillary column (di-isodecyl-phthalate), using 2-chlorophenol as an internal standard. The detection limit was between 0.03-0.08 μg g-1 for the different species considered. Soil samples having carbon contents lower than 5 % can be analyzed by the proposed procedure.
    Additional Material: 4 Ill.
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  • 7
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Each of the hypoxauthine residues of the dinucleoside monophosphate, inosylyl(3′→5′)inosine (IpI), manifests the same rate of deuterium exchange of the proton at the 8-C ring position, as measured by Raman spectrophotometry. In the temperature interval 30-80°C and at neutral pD, the exchange rate constants yield Arrhenius parameters (Ea = 22.4±0.6 kcal mol-1; A = 2.13 × 1013 h-1) that are identical to values obtained on inosine-3′:5′-monophosphate (cIMP), but different from those of inosine-5′-monophosphate (5′-IMP) which exchanges more slowly. The results confirm that nucleotides containing the monovalent phosphate anion, exchange more rapidly than those containing the divalent phosphate anion, and suggest further that base stacking in IpI does not greatly retard the speed of 8-CH exchange of either of the hypoxanthine rings.
    Additional Material: 1 Tab.
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 18 (1987), S. 457-460 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The anisotropic Raman spectra of liquid 1,4-dioxane have been recorded at several temperatures and at different concentrations of aqueous and carbon tetrachloride solutions. The rotational dynamics of the 1,4-dioxane molecules under these conditions is discussed in terms of appropriate correlation functions, reorientational relaxation times and second-order rotational spectral moments.
    Additional Material: 2 Ill.
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  • 9
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The rates (kH) of deuterium exchange of 8-CH groups, as well as the rates (kD) of protium exchange of 8-CD groups in 5′-IMP and cIMP, were measured by laser Raman spectrophotometry over the temperature range 30-80°C. The kH, or ‘forward’ rates, were determined from exchange in D2O solutions, while the kD, or ‘reverse’ rates, were determined from exchange in H2O solutions of the nucleotides. The hypoxanthine nucleotides were found to exchange with rates intermediate between those of corresponding adenine and guanine nucleotides, reported previously. The values obtained for the rate constants as a function of temperature (k=A exp (-Ea/RT)) yield the following Arrhenius activation energies and frequency factors. For 5′-IMP: EaH=25.5±0.6 kcal mol-1, AH=2.61×1015h-1; EaD=24.9±0.6 kcal mol-1, AD=4.32×1014h-1. For cIMP: EaH=22.2±0.6 kcal mol-1, AH=2.52×1013h-1; EaD=21.4±0.6 kcal mol-1, AD=3.93×1012h-1. The lower activation energy for cIMP accounts for its more rapid exchange vis-à-vis 5′-IMP, confirming the trend observed also for adenine and guanine nucleotides. Moreover, as in the cases of adenine and guanine isomers, the differential exchange between cyclic and 5′-nucleotides of hypoxanthine is large at lower temperatures and small at higher temperatures. These results confirm that exchange at 8-C is influenced by the ribosyl phosphate group. The present data also provide evidence of small kinetic isotope effects in the 8-C exchange reactions. For 5′-IMP, kH/kD≈2.5, and for cIMP, kH/kD≈1.7. The isotope effects of 5′-IMP and cIMP are close to the values observed for guanine nucleotides. Finally, Raman vibrational spectra of four isotopic modifications of the hypoxanthine nucleotides are compared to provide specific assignments of the Raman bands to vibrations of the purine skeleton and its exocyclic substituents.
    Additional Material: 5 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 31 (1993), S. 1057-1063 
    ISSN: 0749-1581
    Keywords: 4-Arylflavan-3-ols ; 1H NMR ; 13C NMR ; Circular dichroism ; Condensed tannins ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A unique range of free phenolic 4-arylflavan-3-ols consisting of four sets (3′,4′,5,7-tetrahydroxyflavan-3-ol or its 5-deoxy analogue coupled to phloroglucinol or resorcinol), each composed of three diastereomers (2,3-trans-3,4-trans, 2,3-trans-3,4-cis and 2,3-cis-3,4-trans) were synthesized to assess their spectroscopic properties. 1H and 13C NMR and circular dichroism data are related to selected structural and stereochemical features with a view to modelling natural phenolic oligoflavanoids.
    Additional Material: 2 Ill.
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