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  • 1985-1989  (2)
  • 1970-1974  (4)
  • Organic Chemistry  (5)
  • Microautoradiography  (1)
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  • 1
    ISSN: 1619-7089
    Keywords: Microautoradiography ; Bone tissue ; 99mTc(Sn)-MDP ; 99mTc-MDP ; Hydrolyzed 99mTc
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The localization of 99mTc(Sn)-MDP in bone tissue was compared with 99mTc-MDP by means of microautoradiography of undecalcified bone sections. Sections of good histological quality were obtained by a rapid embedding method in methylmethacrylate. No differences were found in the localization of these radiopharmaceuticals in fetal rat calvariae after incubation in vitro or in rat femora after administration in vivo. In the incubation experiment, hydrolyzed 99mTc was formed. The uptake was high in areas of new bone formation. No uptake was seen in cells or in resorbing areas. In compact bone 99mTc(Sn)-MDP was predominantly taken up in the vicinity of blood vessels.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Using the ‘permutation of indices’ method proposed by Kaplan and Fraenkel, we could formulate the density-matrix equations required to fit the temperature-dependent 13C-NMR spectra observed with the title compounds. For 6Li13CHBr2 (1) and 6Li13CH2SC6H5 (2) an exchange mechanism is proposed by which monomers interchange C- and Li-atoms via a non-observed dimeric intermediate; the activation parameters of these intermolecular dynamic processes have been found to be ΔH≠ = 10.2 kcal/mol, ΔS≠ = 13.7 cal/mol·K for 1 and ΔH≠ = 11.1 kcal/mol, ΔS≠ = 20.6 cal/mol·K for 2 ((D8)THF as solvent). In the case of (6Li)butyllithium (3), the observed low-temperature spectra indicate that dimeric (3b) and tetrameric (3a) species are in dynamic equilibrium interchanging the C3H713CH2 groups (and THF molecules) bonded to the 6Li-atoms. The relative concentrations of the dimer and of the tetramer have been determined by peak integration or by line-shape fitting; the ‘pseudo’- equilibrium constant, defined by K′eq = [3b]2/[3a], was found to be 2.6·10-2 mol/1 (at -88°) and corresponds to ΔGR (-88°) = 2 ΔG°f(3b) - ΔG°f(3a) = 1.34 kcal/mol. The activation parameters of the dynamic process responsible for the exchange were estimated as ΔH≠ = 3.78 kcal/mol and ΔS≠ = -31.3 cal/mol·K. Tentative interpretation of the thermodynamic and kinetic parameters is given.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 57 (1974), S. 2276-2288 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal rearrangement of [18]annulene in solution gives benzene and 1,2-benzo-1,3,7-cyclooctatriene. This reaction has been investigated using a differential scanning calorimeter and the associated enthalpy change has been measured. The enthalpy of the reaction (in the gase phase at 298°K) is \documentclass{article}\pagestyle{empty}\begin{document}$$ \Delta {\rm H}_{\rm r} \left({{\rm g},\,298^ \circ } \right) = - 50.7 \pm 5\,{\rm kcal mol}^{{\rm - 1}} $$\end{document} From this value and the enthalpies of formation of the reaction products, the enthalpy of formation of [18]annulene is obtained: \documentclass{article}\pagestyle{empty}\begin{document}$$ \Delta {\rm H}_{\rm f} \,^ \circ \left({{\rm 1,}\,{\rm g},\,298^ \circ } \right) = 124 \pm 5.5\,{\rm kcal mol}^{{\rm - 1}} $$\end{document} The stabilization energy of [18]annulene, defined as the difference between the enthalpy of formation of the hypothetical Kékulé [18]annulene (with single and double bonds of normal lengths) and the heat of formation of the real molecule is then \documentclass{article}\pagestyle{empty}\begin{document}$$ \Delta {\rm H}_{{\rm stab}{\rm .}} \left({\rm 1} \right) = 37 \pm 6\,{\rm kcal mol}^{{\rm - 1}} $$\end{document} a value close to the corresponding quantity found for benzene.The very large stabilization energy of [18]annulen (100 ± 6 kcal mol-1) previously reported in the literature, based on measurements of the heat of combustion, is not correct since the annulene is certainly oxidized in the bomb prior to combustion.The isodynamic conformational mobility of [18]annulene is not incompatible with a stabilization energy of 37 kcal mol-1; the activation enthalpy observed for this process (ΔH≠ = 16.1 kcal mol-1) indicates that the stabilization is not completely destroyed in the transition state.The mechanism of the thermolysis of [18]annulen, investigated by kinetic measurements and by analysis of the shape of the thermograms, is discussed.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The potential advantages of 13C-(1H-noise decoupled) spectroscopy (in the Fourier transform mode) over 1H-spectroscopy for the quantitative investigation of molecular dynamic process is discussed. The Cope rearrangement in bullvalene, an example of complex exchange of spins over different magnetic sites, has been studied by both kinds of spectroscopy as a test.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 57 (1974), S. 2387-2398 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Heptalene - a very unstable compound - can be reduced by lithium at -80° into its dianion. 1H- and 13C-NMR. studies indicate that this dianion, contrary to the neutral molecule, has its π-bonds delocalized. The magnetic field induces in this species a large diamagnetic ring current. The dianion of heptalene is thermally very stable, much more so than the neutral compound. All these observations point to an appreciable stabilization energy associated with the 14°-electron system; this stabilization energy is probably large enough to impose a planar geometry to this dianion.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Molecules with Fluxional Bonds, XVIII. Bullvalenyl-magnesiumbromide, Bibullvalenyl, Bullvalene Carboxylic acid, Methoxycarbonyl- and MethylbullvaleneThe syntheses and the NMR-spectroscopic behaviour of bullvalenyl-magnesium bromide (2), bibullvalenyl (3), bullvalene carboxylic acid (4), methoxycarbonyl- (5) and methylbullvalene (6) are reported.
    Notes: Es werden die Synthesen und das NMR-spektroskopische Verhalten von Bullvalenyl-magnesiumbromid (2), Bibullvalenyl (3), Bullvalencarbonsäure (4), Methoxycarbonyl- (5) und Methyl-bullvalen (6) beschrieben.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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