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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Phytochemistry 29 (1990), S. 3157-3162 
    ISSN: 0031-9422
    Keywords: Dacrydium bidwillii ; Halocarpus bidwillii ; Podocarpaceae ; foliage oils ; infra-specific variation. ; terpenes
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Phytochemistry 25 (1986), S. 649-653 
    ISSN: 0031-9422
    Keywords: (Z)-5-ethylidene-2(5H)-furanone. ; 8α-isopimara-9(11), 15-diene ; Dacrydium biforme ; Podocarpaceae ; diterpenes ; infraspecific variation ; juvenile-adult dimorphism ; phyllocladene ; sesquiterpenes
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Phytochemistry 26 (1987), S. 839-841 
    ISSN: 0031-9422
    Keywords: Leguminosae ; Lens culinaris ; dansyl chloride. ; ethanolamine, O-acetyl ; isolation: amines ; lentil
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Phytochemistry 29 (1990), S. 3157-3162 
    ISSN: 0031-9422
    Keywords: Dacrydium bidwillii ; Halocarpus bidwillii ; Podocarpaceae ; foliage oils ; infra-specific variation. ; terpenes
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Phytochemistry 26 (1987), S. 3247-3248 
    ISSN: 0031-9422
    Keywords: Leguminosae ; Lens culinaris ; amines ; dansyl chloride. ; imidazole ; lentil
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 23 (1957), S. 387-402 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The mean square length and mean square radius of gyration of 1,4′-polysaccharides and of cis- and trans-polybutadiene were calculated by an extension of the method of Eyring and Benoit, the results being expressed in terms of the degree of polymerization and of certain parameters of physical significance connected with the rotations about the various single bonds in these molecules. The calculations were based on the simplifying assumptions that no correlation exists between rotations about bonds separated by at least one pyranose ring or double bond and that the polysaccharide molecules are made up of pyranose rings in the “chair” form. The excluded volume effect was neglected throughout. The results obtained show that, if the mean square length is plotted against the degree of polymerization, n, then the deviations for small n from the limiting straight line obtained for larger n will have the form of a damped vibration, n appearing instead of the time. In certain cases, however, the results for odd and even n fall on different curves.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 7 (1975), S. 798-798 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 9 (1977), S. 1-12 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions between alizarin yellow G and six different bases B (including OH-) and between tropaeolin 0 and eight different bases have been investigated at 25°C and an ionic strength of 0.5M, using the temperature-jump method. From the form of the log kB versus ΔpK curves it is concluded that for alizarin yellow G the observed relaxation time is due chiefly to a diffusion-controlled reaction between the base and that fraction which is present in the “open” non-hydrogen-bonded form, whereas for tropaeolin 0 the base attacks the hydrogen bridge.The dissociation constants for the internally bound hydrogen have been measured under the same conditions of temperature and ionic strength, using a spectrophotometric method.
    Additional Material: 4 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 39-50 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the reaction between Mg2+ and Eriochrome-Black-T (EBT) has been investigated in the pH range between 7.05 and 9.0, in the presence of 12% ethanol. The reaction is found to consist of two parallel paths, one involving the tervalent unprotonated ligand, and one its monoprotonated form. The rate constant for the unprotonated ligand has a “normal” value, whereas that for the protonated form is much lower. The numerical value of the rate constant for the unprotonated ligand obtained from results at a magnesium concentration of 10-3M and a pH up to 9.0 is, however, inconsistent with that obtained from results at [Mg2+] = (1 to 4) × 10-3M and pH up to 8.1. This can be explained, at least partially, if we assume the intermediate MgHD to lose its proton not only to H2O, but also to other bases present in the solution.
    Additional Material: 3 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 10 (1978), S. 407-415 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the deprotonation of tropaeolin O by OH- ions was investigated between 9° and 30°C, and by OD- ions at 24.7°C. The pH range was 10.7-12.5, and the ionic strength 0.1M throughout. All results were obtained by the temperature jump method. On the basis of a mechanism suggested earlier, rate constants k31 for the reaction between OL- and the internally bonded weak acid and k32 for the opening of the internal hydrogen bond were evaluated. The activation energies in ordinary water were found to be ΔH≠31 = 3.6 kcal/mol, ΔS≠31 = -19 eu, and ΔH≠32 = 27 kcal/mol, ΔS≠32 = 46 eu. The kinetic isotope effect was k31H2O/k31D2O ∼ 1.5 and k32H2O/k32D2O ∼ 0.9. The unusual results for reaction path are discussed in terms of solvent participation.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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