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  • 1
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 9 (1977), S. 121-124 
    ISSN: 0030-4921
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Carbon chemical shifts of cyclic dimethylene compounds were determined and interpreted. It is suggested that steric compression leads to additional shielding of the exo-methylene group, the chemical shifts of this group being a useful measure of the amount of steric hindrance.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 15 (1984), S. 20-28 
    ISSN: 0377-0486
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The line shape observed in coherent Raman scattering (CRS) with excitation under conditions of electronic resonance is discussed, For the case of A-type scattering, the complex Raman amplitude is related directly to the molecular one-photon absorbance of the resonance transition concerned. The basis for this relation is transform theory, a method known from spontaneous resonance Raman scattering to relate the Raman excitation profile to the observed molecular absorbance. Features of the Raman amplitude, determining the observed line shapes for coherent anti-Stokes Raman scattering (CARS) and for coherent Stokes Raman scattering (CSRS), are discussed qualitatively. The discussion considers two typical forms in which broad molecular absorption spectra of polyatomic molecules in the condensed phases appear, Inhomogeneous broadening leads to characteristic changes of the Raman amplitude in relation to molecular absorbance in the case of CSRS (formolecules in the electronic ground state), whereas for CARS the relation derived in the homogeneous broadened case remains valid. The special advantages of the CRS technique for determining the complex non-Raman resonant (background) susceptibility from concentration dependence are demonstrated.
    Zusätzliches Material: 12 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 23 (1985), S. 524-528 
    ISSN: 0749-1581
    Schlagwort(e): Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The 13C NMR data of 42 ring-halogenated oxiranes containing fluorine, chlorine, bromine and, in one case, iodine as substituents are reported and discussed with respect to the influence of the halogen and of other substituents on the chemical shifts of the ring carbon atoms. For monocyclic mono- and dichlorooxiranes increments have been determined which allow the calculation of the chemical shifts of the ring carbon atoms. Comparison of the 13C NMR data of substituted 1,2-dihaloethylenes with those of the corresponding epoxides showed that the signals of the ring carbon atoms of the halogenated oxiranes always appeared at considerably higher field than those of the sp2 hybridized vinylic carbons in the respective precursors.
    Zusätzliches Material: 8 Tab.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
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