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  • Articles  (5)
  • Articles: DFG German National Licenses  (5)
  • Wiley-Blackwell  (5)
  • BioMed Central
  • Cell Press
  • Elsevier
  • Molecular Diversity Preservation International
  • Public Library of Science
  • 1990-1994
  • 1980-1984  (5)
  • 1984  (4)
  • 1981  (1)
  • Chemistry and Pharmacology  (4)
  • Biology  (2)
  • Technology
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  • Articles  (5)
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  • 1990-1994
  • 1980-1984  (5)
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  • Chemistry and Pharmacology  (4)
  • Biology  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 16 (1984), S. 103-115 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the thermal reaction between CF3OF and C3F6 have been investigated between 20 and 75°C. It is a homogeneous chain reaction of moderate length where the main product is a mixture of the two isomers 1-C3F7OCF3 (68%) and 2-C3F7OCF3 (32%). Equimolecular amounts of CF3OOF3 and C6F14 are formed in much smaller quantities. Inert gases and the reaction products have no influence on the reaction, whereas only small amounts of oxygen change the course of reaction and larger amounts produce explosions.The rate of reaction can be represented by eq. (I): The following mechanism explains the experimental results: Reaction (5) can be replaced by reactions (5a) and (5b), without changing the result: Reaction (4) is possibly a two-step reaction: \documentclass{article}\pagestyle{empty}\begin{document}$$ E_1 = 15.90 \pm 0.45{\rm kcal}\,{\rm mol}^{ - 1} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k_1 = \left( {7.60 \pm 0.68} \right)10^8 {\rm exp}\left( { - 15,900\,\, \pm \,\,450\,\,{{{\rm cal}} \mathord{\left/ {\vphantom {{{\rm cal}} {RT}}} \right. \kern-\nulldelimiterspace} {RT}}} \right)M^{ - 1} \cdot s^{ - 1} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ E^ * \, = \,12.30\, \pm \,0.25\,{\rm kcal}\,{\rm mol}^{ - 1} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k^ * \, = \,\left( {6.11\, \pm \,0342} \right)10^7 \,{\rm exp}\left( { - 12,300\, \pm \,250\,{{{\rm cal}} \mathord{\left/ {\vphantom {{{\rm cal}} {RT}}} \right. \kern-\nulldelimiterspace} {RT}}} \right)M^{ - 1} \, \cdot \,{\rm s}^{ - 1} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {E^ * \, - \frac{1}{2}E_1 \, = \,4.35\,{\rm kcal}\, = \,E_3 \, - \,\frac{1}{2}E_4 ;} & {E_3 \,} \\ \end{array} 〉 \,4.35\,{\rm kcal} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ \nu \,\left( {{\rm chain}\,{\rm length}} \right)\, = \,1 + \,\frac{{k_3 }}{{k_1 ^{{1 \mathord{\left/ {\vphantom {1 2}} \right. \kern-\nulldelimiterspace} 2}} \left( {2k_4 } \right)^{{1 \mathord{\left/ {\vphantom {1 2}} \right. \kern-\nulldelimiterspace} 2}} }}\left( {\frac{{\left| {{\rm CR}_{\rm 3} {\rm OF}} \right|}}{{\left| {{\rm C}_{\rm 3} {\rm F}_{\rm 6} } \right|}}} \right)^{{1 \mathord{\left/ {\vphantom {1 2}} \right. \kern-\nulldelimiterspace} 2}} $$\end{document} For ∣CF3 = ∣C3F6∣, ν20°C = 36.8, ν50°C = 24.0, and ν70°C = 14.2.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 508 (1984), S. 79-85 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactions of Dimethyl Sulfoxide with Molybdenum Tetrabromide and Molybdenum Dibromide Dinitrosyl. Crystal Structure of [MoBr2(NO)2(OSMe2)2]In the cold molybdenum tetrabromide reacts with an equivalent amount of dimethyl sulfoxide forming the solvate [MoBr4(OSMe2)2]; excess dimethyl sulfoxide yields [MoO2Br2(OSMe2)2] which is also obtained by other methods. Molybdenum dibromidedinitrosyl forms the solvate [MoBr2(NO)2(OSMe2)2] in the reaction with dimethyl sulfoxide. According to the i.r. spectra all complexes display O-coordination of the OSMe2 molecules. [MoBr2(NO)2(OSMe2)2] crystallizes monoclinic in the space group P21/c with four formula units per unit cell. The cell dimensions are a = 1236, b = 892, c = 1305 pm, β = 95.2°. 1662 independent observed reflexions were used for refinement; R = 3.8%. The molybdenum atoms are six-coordinated, the O atoms of the dimethyl sulfoxide molecules are in trans-position to the nitrosyl ligands, which form linear groups Mo—N—O.
    Notes: Molybdäntetrabromid reagiert mit der äquivalenten Menge Dimethylsulfoxid unter Kühlung zu dem Solvat [MoBr4(OSMe2)2], mit überschüssigem Dimethylsulfoxid entsteht das auch auf anderem Wege zugängliche [MoO2Br2(OSMe2)2]. Molybdändibromiddinitrosyl bildet mit Dimethylsulfoxid das Solvat [MoBr2(NO)2(OSMe2)2]. Nach den IR-Spektren liegen bei allen Komplexen O-Koordination der OSMe2-Moleküle vor. [MoBr2(NO)2(OSMe2)2] kristallisiert monoklin in der Raumgruppe P21/c mit vier Formeleinheiten pro Elementarzelle. Die Gitterabmessungen sind a = 1236, b = 892, c = 1305 pm, β = 95,2° 1662 unabhängige beobachtete Reflexe, R = 3,8%. Das Molybdän ist sechsfach koordiniert, die O-Atome der Dimethylsulfoxidmoleküle befinden sich in trans-Position zu den in gestreckter Bindung koordinierten cis-ständigen Nitrosylgruppen.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Cell Biochemistry and Function 2 (1984), S. 26-32 
    ISSN: 0263-6484
    Keywords: Hormones ; gonadotropins ; Leydig cells ; perfusion ; steroid hydroxylase ; steroid oxidoreductase ; testis ; testosterone ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Production of testosterone by highly purified Leydig cells prepared from rat and mouse testes is compared. Testosterone formation is improved to a higher degree in rat (2.7-fold) than in mouse (1.7-fold) cells by callagenase treatment of the testis compared with mechanical isolation. Mouse Leydig cells respond to exogenous stimuli (chorigonadotropin, dibutyryl cyclic AMP) with 2.4-fold higher testosterone secretion than rat cells. A 1.7-fold increased conversion of androgen precursors to testosterone by mouse compared with rat Leydig cells is demonstrated in static incubations as well as in steady-state superfusion experiments and can be derived from enhanced androstenedione reduction and a less inhibitory effect of progesterone on this process is mouse Leydig cells.
    Additional Material: 5 Ill.
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  • 4
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Introduction of a linear of detectors along the electrophoretic separation space permits monitoring the evolution of electrophoretic zone structures, fully controlled by a microprocessor system. Both transient and steady state zone structures can be recognized. A description of our capillary type apparatus, with 255 potential gradient sensors measuring the most general physical property characterizing the separand pattern in electrophoresis, is given. The central unit of this device is a unique pattern of 256 electrodes. They are chemically photoetched on a supporting glass plate from a vapor-deposited thin layer of a conductor. Each sensor has a width of 60 μm, a height of about 0.1μm and they are spaced 340 μm apart. The whole separation cell, appropriate detection electronics and a new constant current high tension power supply are described together with the microcomputer system used for control and data treatment. Illustrations of detected zone structures with steady state moving boundaries are given in terms of isotachophoretic and moving boundary experiments. The monitoring of non-steady state boundaries is shown by following sample zones in zone electrophoresis.
    Additional Material: 14 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 639-649 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the thermal decomposition of CF3O3CF3 has been investigated in the pressure range of 15-599 torr at temperatures between 59.8 and 90.3°C and also in the presence of CO between 42 and 7°C. The reaction is homogeneous. In the absence of CO the only reaction products are CF3O2CF3 and O2. The rate of reaction is strictly proportional to the trioxide pressure, and is not affected by the total pressure, the presence of inert gases, and oxygen. \documentclass{article}\pagestyle{empty}\begin{document}$$ -\frac{{d[{\rm CF}_{\rm 3} {\rm O}_{\rm 3} {\rm CF}_{\rm 3}]}}{{dt}} = 2\frac{{dp}}{{dt}} = k[{\rm CF}_{\rm 3} {\rm O}_{\rm 3}{\rm CF}_{\rm 3}] $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k = 2.25 \pm 0.18 \times 10^{15} \exp (- 30,530 \pm 130\,{\rm cal}/RT)s^{ - 1} $$\end{document}The following mechanism explains the experimental results: In the presence of CO there appear CO2, (CF3OCO)2, and CF3O2C(O)OCF3 as products. With increasing temperature the amount of peroxicarbonate decreases, while the amounts of oxalate and CO2 increase. The rate of decomposition of the trioxide above a limiting pressure of about 10 torr CO is strictly first order and independent of CO pressure, total pressure, and the pressure of the products. \documentclass{article}\pagestyle{empty}\begin{document}$$ - \frac{{d[{\rm CF}_{\rm 3} {\rm O}_{\rm 3} {\rm CF}_3]}}{{dt}} = k*[{\rm CF}_{\rm 3} {\rm O}_{\rm 3} {\rm CF}_{\rm 3}] $$\end{document} The addition of larger amounts of O2 to the CO containing system chaqnges the course of the reaction.
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