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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 12 (1989), S. 498-500 
    ISSN: 0935-6304
    Keywords: HP-GPC ; HPLC ; GPC ; Asphalts ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 8 (1994), S. 313-316 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The conformation of the rigid isomer pair of cis- and trans-3-pinanones was investigated using methane, isobutane, and ammonia chemical ionization (CI) mass spectrometry as a tool to study the dependence of the mass spectrometric fragmentation patterns. The methane and the isobutane CI mass spectra of the cis and trans isomers were found to be different enough to permit the differentiation of the isomers. Each isomer exhibited distinctive fragmentation paths. The isobutane mass spectra of the cis isomer was dominated by the loss of H2O from the pseudo-molecular ion, whereas the loss of C2H4O was the predominant fragment for the trans isomer. Molecular modeling and quantum-chemical computations were used to calculate the conformers of lowest energy for the two isomers. The theoretical calculations were then used to explain the differences observed in the chemical ionization mass spectra.In addition, high resolution mass spectrometry measurements, deuterium labeling experiments and energy calculations of the hypothetical transition states and ionized species were helpful and were used to propose mechanisms for the CI mass spectral fragmentation.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    X-Ray Spectrometry 15 (1986), S. 83-86 
    ISSN: 0049-8246
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The x-ray fluorescence analysis of trace elements in aqueous solutions requires adequate sample preparation techniques. Aqueous solutions, taken from the environment, often contain chlorides or carbonates, which are likely to produce small crystalline conglomerates in the dried specimen. The use of emulsifiers in the process of specimen preparation was investigated and their advantages demonstrated.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    X-Ray Spectrometry 21 (1992), S. 137-142 
    ISSN: 0049-8246
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Investigations by means of x-ray photoelectron spectrometry, electron probe microanalysis, x-ray fluorescence analysis, imaging x-ray fluorescence analysis, x-ray diffraction and secondary ion mass spectrometry were performed to quantify thin GexCyOz: H films. The films were prepared by r.f. plasma deposition of tetraethylgermanium in a parallel-plate system and in a two-rod discharge system with magnetron enhancement. The results of these investigations indicated that depth profiling delivers a homogeneous composition, with the exception of the outermost surface. At a constant flow-rate of tetraethylgermanium, the film density and the Ge/C atomic ration increase with increasing r.f. power density towards a maximum of 3.5 g cm-3 and 0.5, respectively. The hydrogen content does not change significantly. At low r.f. power densities there is a considerable increase in oxygen. There is no evidence for crystalline germanium carbide. Magnetron enhancement causes an increasing deposition rate and an inhomogeneous deposition in the lateral direction of the films.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0749-1581
    Keywords: 13C NMR spectra ; Coumarins ; Pyranocoumarins ; Khellactones ; Khellactone esters ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C NMR data of several khellactone derivatives are reported. 1H NMR-based stereochemical criteria are evaluated, and a new criterion based on 13C NMR is proposed to establish the relative configuration at C-3′ and C-4′ using ΔδC-3′ between trans and cis isomers and Δδgem(Me)2 values. The structure of trans-4′-methylkhellactone was determined by x-ray analysis.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 25 (1987), S. 203-207 
    ISSN: 0749-1581
    Keywords: 13C NMR ; 1H NMR ; Ranitidine ; E/Z isomerization ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The E/Z configurational equilibrium of the nitroethylenic moiety of the antiulcer agent ranitidine was studied in aqueous solution and in DMSO-d6 and CDCl3 using 1H and 13C NMR spectroscopy. In aqueous solution the room temperature E/Z isomerization of the unprotonated nitroketenediamine moiety is fast on the NMR time scale, but becomes slow for the species protonated at this moiety owing to intramolecular hydrogen bonding between the nitro group and a neighbouring NH2R+ group. In DMSO-d6 a free energy of activation of the order of 70 kJ mol-1 was estimated for the E/Z isomerization of the unprotonated moiety of ranitidine, in good agreement with values previously found for 2,2-disubstituted nitroethylene model compounds.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 22 (1991), S. 217-225 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A confocal Raman microspectrometer was developed for the study of small biological objects such as single living cells and metaphase and polytene chromosomes. It employs a confocal detection scheme, well known from confocal fluorescence microscopes, in order to avoid signal contributions from the environment of the samples. The resolution is 0.45 ± 0.05 μm in the lateral direction and 1.3 ± 0.1 μm in the axial direction. The laser excitation wavelength is 660 nm. At this wavelength biological samples do not degrade in the laser radiation as was the case when laser radiation of 514.5 nm was used. The signal throughput from the sample position to the detector was optimized to the extent that in the spectral region around a 1000 cm-1 Raman shift 15% of the Raman scattered light collected by the microscope objective is detected. For signal detection a liquid nitrogen-cooled slow-scan CCD camera is used. Laser powers of 5-10 mW suffice to obtain high-quality Raman spectra, with signal integration times of the order of minutes. As an example, spectra obtained from the nucleus and the cytoplasm of an intact human lymphocyte are shown.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 26 (1995), S. 663-668 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Raman spectra of the v1(SO42-) band in aqueous solutions of Li2SO4, Na2SO4 and K2SO4 as a function of concentration at room temperature and for fixed concentrations in the temperature range 5 - 85°C were studied. It was found that the molar scattering coefficient for SO42- is virtually independent of the concentration and temperature in the studied range. Nevertheless, the v1(SO42) band shows some asymmetry on the high-wavenumber side for Li and Na and on the low-wavenumber side for K, which for these last two cases has not previously been reported. Moreover, the band position seems to be correlated with the sign and amount of the asymmetry as the concentration increases. On the other hand, temperature does not have a great effect on the band profile. In the case of Na and K, there is little narrowing of the band, whereas for Li there is slight broadening and an increase in the asymmetry. Quantitative analysis of these changes was performed using the vibrational correlation function. This was modelled considering the distribution of sulphate oscillators in the aqueous media as a convolution product of an unperturbed distribution by a perturbation function. This last function assumes a feedback mechanism in which the main parameters are the coupling energy and the fraction of the distribution having interactions. The dependence of these parameters and of the Gaussian and Lorentzian contributions to the band profile with concentration and temperature are discussed.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 2 (1974), S. 351-362 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The resonance Raman spectra of cyano-and aquocobalamin have been obtained from aqueous solutions. In order to check the vibronic theory of Raman intensity in the rigorous resonance case, the excitation profile of the 1502 cm-1 vibration was measured and analyzed using a model of two displaced harmonic oscillators for the ground and the resonant electronic state. A very good agreement is shown between the calculated and the experimental values of both the excitation profile and the absorption spectrum. Information on the corrin ring symmetry and evaluation of the vibronic interaction energies have been obtained. The appearance of several overtones and combinations is also reported.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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