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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Molecular and Cellular Endocrinology 46 (1986), S. 109-119 
    ISSN: 0303-7207
    Keywords: LHRH ; cultured gonadotrophs ; gonadotrope polypeptide GP-87 induction ; pituitary
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0167-0115
    Keywords: LHRH ; atrial natriuretic factor ; atriopeptin ; cyclic GMP ; gonadotrophs ; sodium nitroprusside
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 24 (1986), S. 429-429 
    ISSN: 0887-6258
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 6 (1983), S. 20-26 
    ISSN: 0935-6304
    Keywords: Reversed-phase mode liquid chromatography ; Rekker's hydrophobic fragmental constant ; Calculation of concentration of organic modifier ; Prediction of retention time of phenols ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The chromatographic behavior of phenols in reversed-phase mode liquid chromatography differs from that of non-ionic compounds such as alkyl alcohols, alkylbenzenes, halogenated benzenes, polyaromatic hydrocarbons, and aromatic acids. Therefore, the retention times of 61 phenols were measured in a system of an octadecyl bonded silica gel and acetonitrile/water mixtures. The logarithm of the capacity ratio (log k') was found to be a linear function of the hydrophobicity (log P) in acidic acetonitrile/water mixtures. This result was applied to a different octadecyl bonded silica gel. Eight phenols were selected as standard compounds, and their log k' values were measured in 0.05 M phosphoric acid in 10 to 90% acetonitrile/water mixtures. An empirical polynomial relation was obtained between the concentration of acetonitrile and the slope of the log k' vs log P curve. Finally the capacity ratio of all phenols were calculated in given eluents by the equations derived from the measurements of standard compounds and the calculated log P values. The difference between predicted capacity ratios and measured ones was within 10%.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 4 (1981), S. 454-460 
    ISSN: 0935-6304
    Keywords: Reversed-phase mode liquid chromatography ; Rekker's hydrophobic fragmental constant ; Calculation of concentration of organic modifier ; Prediction of retention time ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The utility of Rekker's hydrophobic fragmental constant has been examined for optimization of reversed-phase mode liquid chromatographic separations. The chromatographic behavior of about 60 non-ionic compounds was measured in different acetonitrile/water mixtures and the logarithm of their capacity factors (log k) was correlated with their calculated hydrophobicities (log P). Linear relations were found in each case between log k and log P. The slope of the various lines was related to the percentage concentration of acetonitrile in the mobile phase. It was shown that, by using nine stand ard compounds and measuring their capacity factors in five eluents with different acetonitrile concentrations, the retention time could be predicted for 60 compounds. Calculation of the concentration of the organic modifier was also possible in a system of well coated octadecyl bonded packings with acetonitrile/water mixtures as eluent. Prediction of the capacity factor was accomplished to within 5% error.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2179-2193 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Crosslinking of linear poly[2,2′-(1,4-phenylene)-6,6′-bis(3-phenylquinoxaline)] (PPQ) by isothermal heat exposure in the temperature range between 425 and 490°C was investigated by means of torsional braid analysis. The change in glass transition temperature due to isothermal exposure was used as a kinetic parameter. In order to determine the effect of molecular weight and type of polymer chain ends, three PPQ samples were prepared that differed only in molecular weight and polymer chain endgroups. The apparent activation energy of isothermal crosslinking was independent of molecular weight and chain endings. Its value of 60 kcal/mole is the same as that for the thermal degradation of PPQ (determined by isothermal weight loss measurements). The rates of change of Tg at a particular temperature, however, are a function of both molecular weight (at least for these polymers that do not have a sufficiently high molecular weight) and the type of polymer chain ends. It was observed that isothermally crosslinked PPQ gave a higher break point in the TGA curve and also an increased char yield at 800°C than the linear precursor.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2195-2207 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Linear polyphenylimide-quinoxalines (PPIQ) can be crosslinked by isothermal heat treatment in an inert atmosphere. To show this, three polyphenylimide-quinoxalines were prepared which differed only in molecular weight and polymer chain endings. Apparent activation energies of thermal crosslinking were then obtained from the rates of change of Tg as a function of time and temperature. The values (60 kcal/mole) were essentially the same as those for the thermal degradation of the same polymer in vacuum. Differences in polymer molecular weight had a distinct effect on the rates of change of Tg but the polymer chain ends seemed to have a lesser effect than previously observed on polyphenylquinoxalines (PPQ). Nevertheless, the rate of change in Tg is greater for PPIQ than for PPQ of a similar molecular weight. This indicates that the imide portion of the polymer chain leads to faster crosslinking under isothermal conditions.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 19 (1981), S. 463-467 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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