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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: 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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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 750 (1971), S. 136-148 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Ditropylium IonDitropylium dihexachloroantimonate (6) has been prepared in over 70 per cent yield by reaction of antimony pentachloride with heptafulvalene (5). The possible mechanisms of this reaction as well as the 1H-NMR-, 13C-NMR-, UV- and IR-spectra of 6 are discussed. HMO and ω-technique-calculations are performed and correlated with experimental data.
    Notes: Das Ditropylium-dihexachloroantimonat (6) wird durch Umsetzung von Heptafulvalen (5) mit Antimonpentachlorid in über 70proz. Ausbeute dargestellt. Die für die Reaktion wahrscheinlichen Bildungsmechanismen sowie die 1H-NMR-, 13C-NMR-, UV- und IR-Spektren von 6 werden diskutiert. Sowohl für 5 als auch für 6 werden Berechnungen nach der HMO-Methode sowie der ω-Technik ausgeführt und diese mit den experimentellen Daten korreliert.
    Additional Material: 5 Ill.
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  • 4
    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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  • 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
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 54 (1971), S. 343-351 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: L'actylamino-5-thiophénecarbaléhyde-2, dont la préparation a été a améliorée, a été condensé avec des corps à méthylène actif. Certains des produits obtenus ont servi è prépaparer des acides aminés thiophéniques puis finalement le monochlorhydrate d'homolysine, corps nouveau. La condensation de l'acétylamino-5-thiophénecarbaldéhyde-2 avec l'acide malonique a fourni non pas l'acide propionique ß-aminé correspondant, mais l'acide (acétylamino-5-thénylidène-2)-malonique.
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  • 7
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Analysis of the photoelectron spectrum of homofulvene (1) (spiro [2.4] hepta-4,6-diene) confirms the conclusions previously drawn concerning the direct conjugation between π-and Walsh-orbitals. It is shown that the resonance integral (4) appropriate for the semi-quantitative interaction of these orbitals amounts to -1.9 eV, i.e. nearly the value for conjugating π-orbitals (β = -2.4 to -2.5 eV). This explains the close analogy between the photoelectron spectrum of 1 and that of fulvene.
    Additional Material: 2 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 54 (1971), S. 2111-2113 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: On UV.-irradiation in strongly acidic solution 3-alkyl- and 3-aryl-2,1 benzisoxazoles, respectively, yield 5-substituted 2-aminophenylketons.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 56 (1973), S. 1594-1604 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: To obtain further information concerning the interaction between Walsh-orbitols of ‘conjugated’ cyclopropane rings, the photoelectron spectra of the following compounds have been recorded: bicyclo[4.1.0]heptane 1, cis- and trans-tricyclo[5.1.03, 5]octane 2, 3, diademane 4, trans-pentacyclo[3.3.2.02, 9.04, 10, 06, 8]decan 5 and bicyclo[4.1.0]heptene-2 6. The first bands in the PE.-spectra of these compounds have been assigned on the basis of a ZDO HMO-approximation. For 2 and 4 the value for resonance integral between linked 2p atomic orbitals of two adjacent eclipsed cyclopropane rings is found to be -1.73 eV.
    Additional Material: 2 Ill.
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  • 10
    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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