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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 1 (1974), S. 295-295 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 11 (1978), S. 535-540 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A data base containing approximately 4000 13C nuclear magnetic resonance spectra has been assembled. The spectra have been evaluated and all the corresponding compounds have been registered by the Chemical Abstracts Service (CAS). The data base is available to the international scientific community on magnetic tape or microfiche and is also the basis of a search system operating upon an international computer network.
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 17 (1982), S. 547-552 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Over 1400 electron ionization mass spectra of selected organic compounds have been measured under carefully defined conditions. In this paper, the variables such as sample purity and spectrometer calibration that are controlled are described. The quality of the resulting spectra as well as the cost of the measurements is reported.
    Additional Material: 2 Ill.
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  • 4
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 12 (1979), S. 289-296 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A link between a substructure searching system and a 13C NMR data base has been established and permits the retrieval and examination of the chemical shifts associated with specific substructures. The means by which these searches are accomplished is described and the results from the searches are presented and discussed. The system is interactive, and can be used to locate in the data base the chemical shifts of carbon atoms in precisely defined environments. Alternatively, it may be used to learn the range of the chemical shifts possessed by particular types of carbon atoms, such as N-methyl or O-methyl carbons.
    Additional Material: 5 Ill.
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  • 6
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Cobalt Chelates as Hydrogenation Catalysts. VI. Spectrophotometric Investigation of the Adduct Formation of [Co(dpnH)]+ with PyridineThe investigation of the adduct formation of the [Co(dpnH)]+ complex with pyridine by spectrophotometric measurements causes some difficulties due to the unfavourable overlapping of the spectra of the starting complex, the mono- and the bis-adduct in the spectral range used (17000-32000 cm-1). Therefore, the adduct formation constant β2 can only be determined, if the waveleagths for the evaluation of the data are suitably selected. The thermodynamic parameters, calculated from the temperature dependence of β1 (δRH° = -9.1 ± 0.5 kJ · mol-1, δRS° = -5.6 ± 1.7 J · mol-1 · K-1), differ clearly from those which have been obtained from kinetic measurements [3]. The reason for this difference, which is quite beyond the error limit of the applied methods, is most probably the neglect of analogous adduct equilibria with the solvent.
    Notes: Die Untersuchung der Adduktbildung des [Co(dpnH)]+-Komplexes mit Pyridin durch spektralphotometrische Messungen bereitet Schwierigkeiten, da sich die Spektren des Ausgangskomplexes, des Mono- und des Bis-Addukts im untersuchten Spektralbereich (17000-32000 cm-1) ungünstig überlagern. Die Adduktbildungskonstante β2 läßt sich daher nur ermitteln, wenn die Wellenzahlen für die Auswertung der Messungen geeignet ausgewählt werden. Die aus der Temperaturabhängigkeit von β1 berechneten thermodynamischen Parameter (δRH° = -9,1 ± 0,5 kJ · mol-1, δRS° = -5,6 ± 1,7 J · mol-1 · K-1) unterscheiden sich jedoch deutlich von den Werten, die durch kinetische Messungen [3] bestimmt worden sind. Ursache für diese, weit außerhalb der Fehlergrenze der Methoden liegenden Differenzen ist sehr wahrscheinlich die Vernachlässigung von analogen Adduktgleichgewichten mit dem Lösungsmittel.
    Additional Material: 4 Ill.
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  • 7
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Cobalt Chelates as Hydrogenation Catalysts. III. Hydride Formation of the [Co(dpnH)]+ Catalyst in the Presence of Pyridine as Axial BaseThe rate of the hydrogen uptake for [Co(dpnH)]+ is 2nd order with respect to the complex concentration and depends on the amount of added pyridine, in accord with the assumption of a more active mono- and an inactive bis-pyridine adduct. The rate law, formulated on this basis agrees very well with the measured data. The ΔH≠ - and ΔRH°-values, calculated from the temperature dependence of the rate constants and equilibrium constants are in agreement with the suggested model, whereas the ΔS≠ and ΔRS° values do not correspond completely with these expectations.
    Notes: Die Geschwindigkeit der Wasserstoffaufnahme des [Co(dpnH)]+-Komplexes ist 2. Ordnung bezüglich der Komplexkonzentration und abhängig von der Menge an zugesetztem Pyridin, in Übereinstimmung mit der Annahme eines aktiveren Mono- und eines inaktiven Bis-Pyridinaddukts. Das auf dieser Basis formulierte Geschwindigkeitsgesetz steht in sehr guter Übereinstimmung mit den Meßwerten. Die aus der Temperaturabhängigkeit der Geschwindigkeits- bzw. Gleichgewichtskonstanten berechneten ΔH≠- und ΔRH°-Werte stimmen mit dem angenommenen kinetischen Modell überein, während die ΔS≠- und ΔRS°-Werte diesen Erwartungen nicht ganz entsprechen.
    Additional Material: 5 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 536 (1986), S. 65-76 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Cobalt Chelates for Hydrogenation Catalysts. II. Hydride Formation with [Co(dmgH)2] and [Co(dpnH)]+In the presence of benzil as scavanger for the hydridocomplexes [Co(dpnH)]+ and [Co(dmgH)2] the hydride formation in water/n-propanol (50% v/v) becomes the rate determining step, and the ligand hydrogenation is completely suppressed in the case of [Co(dpnH)]+, but only partially in the case of [Co(dmgH)2]. The rate of hydride formation in both cases is 2nd order with respect to the complex, and the activation parameters ([Co(dmgH)2]: ΔH≠ = 48.4 ± 1.0 kJ · mol-1, ΔS≠ = -57.4 ± 3.4J · mol-1 · K-1, [Co(dpnH)]+: ΔH≠ = 52.7 = 0.4 kJ · mol-1, ΔS≠ = -59.8 ± 1.2J · mol-1 · K-1) indicate a H2-activation by homolytic splitting for both complexes. Some sources of error and possible causes for the missing activity of [Co(tim)]2+ are discussed.
    Notes: In Gegenwart von Benzil als Abfangreagens für die Hydridokomplexe [HCo(dpnH)]+ und [HCo(dmgH)2] wird die Hydridbildung in Wasser/n-Propanol (50% v/v) zum geschwindigkeitsbestimmenden Schritt und die Ligandhydrierung beim [Co(dpnH)]+ vollständig, beim [Co(dmgH)2] nur noch teilweise unterdrückt. Die Hydridbildungsgeschwindigkeit ist in beiden Fällen 2. Ordnung bezüglich des Komplexes und die Aktivierungsparameter ([Co(dmgH)2]: ΔH≠ = 48,4 = 1,0 kJ · mol-1, ΔS≠ = -57,4±3,4J · mol-1 · K-1, [Co(dpnH)]+: ΔH≠ = 52,7 ± 0,4 kJ · mol-1, ΔS≠ = -59,8 ± 1,2J · mol-1 · K-1) sprechen bei beiden Komplexen für eine H2-Aktivierung durch homolytische Spaltung. Einige Fehlerquellen und mögliche Ursachen für die fehlende Aktivität beim [Co(tim)]2+ werden diskutiert.
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