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  • Articles: DFG German National Licenses  (4)
  • 1980-1984  (1)
  • 1970-1974  (3)
  • Physical Chemistry  (3)
  • Sheep  (1)
Source
  • Articles: DFG German National Licenses  (4)
Material
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 217 (1981), S. 211-223 
    ISSN: 1432-0878
    Keywords: Pituitary gland ; Pars intermedia ; Electron microscopy ; Sheep
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Light microscopy of coronal sections of the sheep pars intermedia revealed a compact, incompletely lobulated V-shaped region about 15–20 cells thick, situated between the pars distalis and the pars nervosa. A prominent hypophysial cleft and follicles containing a colloid-like substance were seen. Using electron microscopy, five cell types could be distinguished: pars intermedia glandular cells, pars distalis-like glandular cells, interstitial cells, follicular cells and cleft lining cells. The polyhedral to pear-shaped pars intermedia glandular cells predominated. They contained dense-cored, membrane-bound granules near the Golgi complex, and larger, irregular vesicles with finely granular contents of varying electron density throughout the remaining cytoplasm; exocytotic release of granules was occasionally observed. Smaller numbers of cells resembling those seen in the pars distalis were scattered throughout the pars intermedia. Interstitial cells usually possessed elongated cytoplasmic processes which extended between the glandular cells, and were characterized by deeply indented nuclei, elaborate junctional complexes and an absence of cytoplasmic granules. Cells lining the follicles resembled the interstitial cells. The major cells bordering the hypophysial cleft were triangular in section and bore irregular microvilli on their free surface. The pars intermedia appeared to be less vascular than the remainder of the hypophysis and only occasional fenestrated capillaries were seen. Nerve profiles were rare.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 5 (1973), S. 137-147 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cyclopropyl cyanide isomerizes in the gas phase at 660°-760°K and 2-89 torr to give mainly cis- and trans-crotonitrile and allyl cyanide, with traces of methacrylonitrile. The reactions are first order, homogeneous, and unaffected by the presence of radical-chain inhibitors. The rate constants are given by Overall: \documentclass{article}\pagestyle{empty}\begin{document}$$\log _{10} k/{\rm sec}^{ - 1} = (14.58 \pm 0.08) - (242.0 \pm 1.2){\rm kJ}\,{\rm mole}^{ - 1} /2.303RT$$\end{document} cis-Crotonitrile: \documentclass{article}\pagestyle{empty}\begin{document}$$\log _{10} k/{\rm sec}^{ - 1} = (14.01 \pm 0.11) - (237.6 \pm 1.4){\rm kJ}\,{\rm mole}^{ - 1} /2.303RT$$\end{document} trans-Crotonitrile: \documentclass{article}\pagestyle{empty}\begin{document}$$\log _{10} k/{\rm sec}^{ - 1} = (14.09 \pm 0.07) - (243.7 \pm 0.9){\rm kJ}\,{\rm mole}^{ - 1} /2.303RT$$\end{document} Allyl cyanide: \documentclass{article}\pagestyle{empty}\begin{document}$$\log _{10} k/{\rm sec}^{ - 1} = (14.59 \pm 0.13) - (252.0 \pm 1.8){\rm kJ}\,{\rm mole}^{ - 1} /2.303RT$$\end{document} where the error limits are standard deviations. On the basis of a biradical mechanism, it is deduced that the —CH—CN radical center is resonance stabilized by ca. 30 kJ mole-1. Approximate equilibrium data are given for interconversion of the 1- and 3-cyanopropenes.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 5 (1973), S. 329-331 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The high-pressure isotopic rate ratio kH/kD for isomerisation of cyclopropylamine and cyclopropylamine-N-d2 is 1.06 at 649-678 K, supporting a mechanism which does not involve migration of hydrogen from the amine group in the rate-determining step.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 5 (1973), S. 27-35 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: At temperatures of 356-425°C and pressures of 15-60 Torr, cyclopropylamine reacts to give an equimolar mixture of ammonia and N-propylidenecyclopropylamine as the initial product. The reaction is first order, homogeneous, and unaffected by the presence of radical inhibitors, and thus proceeds by an initial rate-determining unimolecular isomerization to give a reactive intermediate, which then reacts with a further molecule of cyclopropylamine to give the observed products. Reaction in the presence of added aliphatic amines gives other imines in addition, and the nature of these indicates that the intermediate is propenylamine or its tautomer propylideneamine:
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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