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  • Organic Chemistry  (8)
  • Physics  (6)
  • Wiley-Blackwell  (14)
  • 1975-1979  (8)
  • 1970-1974  (6)
  • 1965-1969
  • 1975  (8)
  • 1974  (6)
Collection
Publisher
  • Wiley-Blackwell  (14)
Years
  • 1975-1979  (8)
  • 1970-1974  (6)
  • 1965-1969
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  • 1
    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.
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  • 2
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photoelectron spectra of spiro[3.4]octane (1), spiro[3.4]octene-5 (2), spiro[3.4]-octa-5,7-diene (3), spiro[4.4]nonene-2 (4) and spiro[4.4]nona-2,4-diene (5) have been recorded. The first bands of these spectra are correlated with orbitals which are π-orbitals, Walsh orbitals resp. linear combinations of both. Our assignment is based on a qualitative ZDO-model, it is in satisfactory agreement with the results of extended Hückel calculations. The interaction found in 2 and 3 is of similar magnitude as the one in 4 and 5 and considerably less than that in homofulvene and fulvene.
    Additional Material: 6 Ill.
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  • 3
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: By condensation of the chlorides of the four isomeric fluorenecarboxylic acids, respectively of the three 1-, 3- and 4-fluorenonecarboxylic acids with fluorene, followed by reduction of the obtained mono-respectively diketones, the four difluorenylmethanes I, II, III and IV are synthesized. The oxydation of the diketones gives the corresponding triketones. Starting from the chloride of 4-fluorenecarboxylic acid and 1-methylfluorene, a methyl derivative of IV is analogically obtained.
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  • 4
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A synthetic approach to a variety of monomeric Vinca alkaloids is described. The sequence involves, among its crucial phases, the generation of appropriate nine-membered ring intermediates which are then elaborated via a transannular cyclization approach to the desired natural products.
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  • 5
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Schiff'sche Basen aus Stilben-4-carbaldehyd, 2-(p-Formyl-phenyl)-benzo[b]furan und 2-Phenyl-6-formyl-benzo[b]furan und p-Chloranilin können mit p-tolyl- bzw. methyl-substituierten heterocyclischen und carbocyclischen Aromaten in Gegenwart von Dimethylformamid und Kaliumhydroxid bzw. Kalium-t-butylat in die entsprechenden Stilben-bzw. Styrol-Derivate übergeführt werden («Anil-Synthese»).Die Lage der Absorptions- und Fluoreszenz-Maxima der dargestellten Grundkörper der Benzo[b]furan-Reihe wird mit derjenigen entsprechender Stilben-Verbindungen verglichen.
    Additional Material: 41 Tab.
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  • 6
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Partial molar excess free enthalpies (or excess chemical potentials) at infinite dilution were obtained over a large temperature range by gas chromatography. Data on n-alkenes in Apiezon M are interpreted by the Prigogine-Patterson theory; data on normal and branched alkanes in squalane and polydimethylsiloxane (PDMS) are discussed in terms of the Prigogine-Patterson theory and the solution theory of Flory, Orwoll, and Vrij. For the alkane-PDMS systems heats of dilution and partial excess heat capacity data are given.The aim of this work is to get some insight in the applicability of these solution theories to mixtures of fluids, the properties of which may slightly violate the basic assumptions of these theories. It is shown that orientational order in and a large cross-sectional chain diameter of the polymer solvent do not affect their applicability to the partical molar excess free enthalpies of apolar mixtures, whereas large dissimilarities between the force fields around the segments of the mixture components and/or dissimilar chain flexibilities detract from the applicability of these theories (alkanes in PDMS).Special attention has been paid to the effects of dissimilar size and shape of the segments of the mixture compounds on the magnitude of the interchange interaction parameter. It is shown that the multiple-connected segment model after Lichtenthaler et al. does not warrant a reliable combinatorial contribution. Comparison of the interaction parameters obtained for n-alkanes in n-alkanes, Apiezon, squalane, and polyisobutylene and for branched alkanes in squalane reveals that the magnitude of this parameter is affected by small end-effects due to the relative weakness of methyl-methylene interactions.
    Additional Material: 3 Ill.
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  • 7
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Components of the Green Deathcap Toadstool, Amanita phalloides, XLV1). - The Absolute Configurations of the Toxic and Nontoxic Phalloidin Sulfoxide and of the Amatoxins2ind-Ethylthio-L-tryptophan (2a) synthesized from L-tryptophan and ethyl sulfenyl chloride is oxidized by H2O2 in glacial acetic acid to give the two diastereoisomeric sulfoxides 2b and 2c, which can be separated from each other. Crystals of 2b are subjected of X-ray analysis, which reveals R-configuration at the chiral SO center. By analogy with the ORD curve of 2b having positive values between 280 and 360 nm (figure 3), the toxic phalloidin sulfoxide 1b (figure 4) can be assigned the same configuration. Since comparable amatoxins (amanin, O-acetyl-γ-amanitin) show very similar behaviour in ORD the R-configuration at the SO-center is established also in this series of toxins.
    Notes: 2ind-Äthylthio-L-tryptophan (2a) wurde aus L-Tryptophan und Äthylsulfenylchlorid synthetisiert und mit H2O2 in Eisessig zu den zwei diastereomeren Sulfoxiden 2b und 2c oxidiert, die getrennt und kristallisiert wurden. Für die Kristalle von 2b zeigt die Röntgenstrukturanalyse R-Konfiguration am chiralen So-Zentrum an. Durch den analogen Verlauf der ORD-Kurve von 2b, die zwischen 280 und 360 nm positive Werte hat (Abbildung 3), und der des giftigen Phalloidinsulfoxids 1b bestimmt. Da vergleichbare Sulfoxide de Amatoxinreihe (Amanin, O-Acetyl-γ-amanitin) ähnliche ORD-Kurven geben, ist auch deren R-Konfiguration am SO-Zentrum erwiesen.
    Additional Material: 4 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 835-850 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A systematic study of the dispersion curves of the refractive indexes of nylon 6 yarns was made. The parameters were the draw ratio and strain. The measurements show that the dispersions of the refractive indexes n∥ and n⊥, parallel and perpendicular to the fiber axis, are equal, independently of draw ratio and strain. The average dispersion equals nF - nC = 109 × 10-4. Consequently, the birefringence is, within experimental accuracy, independent of the wavelength. The refractive indexes and the birefringence show a change in trend at 10-12% strain. This point corresponds to the yield strain in the stress-strain diagrams. The inference is that beyond the yield point the overall molecular orientation must increase less strongly with strain than before. An analysis shows that the Lorentz-Lorenz relation holds for the average refractive index n̄ = ⅓ (n∥ + 2n⊥). So the change in n̄ versus draw ratio is mainly due to the change in density. By applying the Lorentz-Lorenz relation to the change of n̄ on straining, a value of Poisson's ratio (μ) could be derived. The average value found for nylon 6 yarns was μ = 0.48, which means that the density hardly changes with strain.
    Additional Material: 8 Ill.
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  • 9
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Rotational Isomerism of Bicyclopropyl, I. - IR- and NMR-spectroscopic Investigations of Bicyclopropyl, Octadeuteriobicyclopropyl and Some Bicyclopropyl Derivatives**The rotational isomerism of the bicyclopropyl (10) molecule has been investigated by measuring the temperature dependence of 1) the infrared band intensities of the two conformers and 2) the vicinal coupling constant between the two methine protons. The results of the two methods agree in that the gauche (synclinal) conformer is more stable than the s-trans (antiplanar) form by about 150 cal/mol. - The 1H-NMR parameters of the pure conformers, which were necessary to evaluate the temperature dependent NMR data in terms of the changes in the population of different conformers, were obtained from the spectra of suitable sterically hindered bicyclopropyl derivatives. -A comparison of the experimental results with a theoretical torsional potential energy curve calculated on the basis of van der Waals interactions between nonbonded atoms clearly shows that the possible electronic interaction between the Walsh orbitals of the two cyclopropyl groups does not influence the conformational equilibrium in bicyclopropyl to any significant extent.
    Notes: Zur Untersuchung der Rotationsisomerie des Bicyclopropyls (10) wurden Intensitätsmessungen an IR-Schlüsselbanden der beiden Konformeren bei verschiedenen Temperaturen vorgenommen und es wurde die Temperaturabhängigkeit der Vicinalkopplungskonstanten zwischen den beiden Methinprotonen ermittelt. Beide Verfahren ergeben übereinstimmend, daß das gauche-Konformere (synclinale Form) in flüssiger Phase um ca. 150 cal/mol stabiler ist als die s-trans-Form (antiplanare Form). - Die für die Auswertung der 1H-NMR-Daten erforderlichen Grenzwerte für die Vicinalkopplungskonstante der reinen Konformeren wurden durch Messungen an geeigneten sterisch gehinderten Bicyclopropyl-Derivaten gewonnen. - Der Vergleich der Ergebnisse mit einer auf der Grundlage von van-der-Waals-Potentialen berechneten Torsionspotentialkurve macht deutlich, daß beim Bicyclopropyl die mögliche elektronische Wechselwirkung zwischen den Walsh-Orbitalen der beiden Dreiringe ohne bestimmenden Einfluß auf die Lage des Konformeren-Gleichgewichtes bleibt.
    Additional Material: 3 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1975 (1975), S. 1945-1951 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Stable Carbenium Ions, XX.  - Aryl(dich1oro)carbenium Ions  - a Study on the Structure of an Extraordinary Dicarbenium IonDichloro(mesityl)carbenium-, dichloro(phenyl)carbenium- and mesitylenecarbonylium hexachloroantimonate (4′, 6 and 8′, resp.) were prepared as crystalline salts and chemically and spectroscopically characterized. It could be shown that the extraordinary dicarbenium ion 2, discussed by Hart and coworkers3, is in fact the dichloro(mesityl)carbenium ion (4).
    Notes: Das Dichlor(mesityl)carbenium-, das Dichlor(phenyl)carbenium- und das Mesitylencarbonylium-hexachloroantimonat (4′, 6 bzw. 8′) wurden in Form kristalliner Salze dargestellt und sowohl chemisch als auch spektroskopisch charakterisiert. Es konnte gezeigt werden, daß das von Hart und Mitarbeitern3 diskutierte außergewöhnliche Dicarbeniurnion 2 in Wirklichkeit das Dichlor(mesityl)carbeniumion (4) ist.
    Additional Material: 3 Tab.
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