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  • 1985-1989  (15)
Material
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 89 (1985), S. 2914-2916 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 90 (1986), S. 4408-4413 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 90 (1986), S. 4637-4640 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 89 (1985), S. 1690-1692 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 89 (1985), S. 4596-4600 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 502 (1987), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 19 (1987), S. 659-678 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The pyrolysis of acetylene-styrene mixtures has been studied from 450-550°C in a quartz reaction vessel in the absence and presence of O2 or NO. The rates of disappearance of reactants and formation of adducts are first-order in each reactant. The major product is polymer, with the adducts accounting for about 2.5% and 6.2% of the styrene removed at 450 and 550°C, respectively. The acetylene-to-styrene removal ratio is about 27 independent of temperature. The adducts formed are methyl indene and 1,2-dihydronaphthalene. These are about half-suppressed in the presence of O2 or NO. The rate coefficients for reactant removal and adduct formation are: \documentclass{article}\pagestyle{empty}\begin{document}$$ \log \{ k\{ {\rm C}_{\rm 2} {\rm H}_{\rm 2} \},M^{ - 1} {\rm s}^{ - 1} \} = 7.53 \pm 0.10 - (90.6 \pm 1.5)/2.3RT $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ \log \{ k\{ {\rm C}_{\rm 8} {\rm H}_{\rm 8} \},M^{ - 1} {\rm s}^{ - 1} \} = 6.63 \pm 0.60 - (98.5 \pm 8.8)/2.3{\rm }\,RT $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ \log \{ k\{ {\rm C}_{{\rm 10}} {\rm H}_{{\rm 10}} \},M^{ - 1} {\rm s}^{ - 1} \} = 8.27 \pm 0.66 - (143.3 \pm 9.8)/2.3RT $$\end{document} where the activation energies are in kJ/mol and the uncertainties are one standard deviation. As the reaction proceeds, the methyl indene and 1,2-dihydronaphthalene decompose, and indene and naphthalene are formed. In addition, an unidentified isomer of naphthalene is produced as an initial minor product, and it also decomposes as the reaction proceeds.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 21 (1989), S. 175-191 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2-Methylbut-1-ene-3-yne and Propyne mixtures were pyrolyzed at 350-450°C in the absence and presence of O2 and NO. The major product of the reaction is a polymer, but m-xylene and p-xylene are also produced and were studied as the species of interest. The C8H10 formation rate is first-order in C3H4 and C5H6. The rate coefficient is best fitted by \documentclass{article}\pagestyle{empty}\begin{document}$$\log [k({\rm C}_{\rm 8} {\rm H}_{{\rm 10}}),M^{ - 1} s^{ - 1}] = (11.2 \pm 1.0) - (166 \pm 13)/2.3RT$$\end{document} though it is not inconsistent with \documentclass{article}\pagestyle{empty}\begin{document}$$\log [k({\rm C}_{\rm 8} {\rm H}_{{\rm 10}}),M^{ - 1} s^{ - 1}] = (8.17) - (125.9)/2.3RT$$\end{document} where R is the ideal gas constant in kJ/mol-K. Experiments in the presence of NO show that m-xylene and p-xylene formation occur by two processes: a concerted molecular mechanism (≃ 41%) and a singlet diradical mechanism (≃ 59%).
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 17 (1985), S. 503-524 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: i-C4H9ONO was photolyzed with 366-nm radiation at -8, 23, 55, 88, and 120°C in a static system in the presence of NO, O2, and N2. The quantum yield of i-C3H7CHO, Φ{i-C3H7CHO}, was measured as a function of reaction of reaction conditions. The primary photochemical act is and it proceeds with a quantum yield φ1 = 0.24 ± 0.02 independent of temperature. The i-C4H9O radicals can react with NO by two routes The i-C4H9O radical can decompose via or react with O2 via Values of k4/k2 ≃ k4b/k2 were determined to be (2.8 ± 0.6) × 1014, (1.7 ± 0.2) × 1015, and (3.5 ± 1.3) × 1015 molec/cm3 at 23 55, and 88°C, respectively, at 150-torr total pressure of N2. Values of k6/k2 were determined from -8 to 120°C. They fit the Arrhenius expression: \documentclass{article}\pagestyle{empty}\begin{document}$$ \log (k_6 /k_2) = - 2.15 \pm 0.22 - (836 \pm 159)/2.303{\rm T} $$\end{document} For k2 ≃ 4.4 × 1011 cm3/s, k6 becomes (3.2 ± 2.0) × 10-13 exp{-(836 ± 159)/T} cm3/s. The reaction scheme also provides k4b/k6 = 3.59 × 1018 and 5.17 × 1018 molec/cm3 at 55 and 88°C, respectively, and k8b/k8 = 0.66 ± 0.12 independent of temperature, where
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 17 (1985), S. 535-546 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The alkyl nitrites, C2H5ONO, n-C3H7ONO, n-C4H9ONO, and i-C4H9ONO were photolyzed at 23°C in the presence of 15NO at 366-nm incident radiation. The quantum yields of the corresponding isotopically-enriched alkyl nitrites were measured by mass spectrometry. The results indicated that only part of the absorption leads to photodecomposition. The remainder forms an electronically excited state which isotopically exchanges with 15NO. The indicated reactions of the electronically excited state RONO*, are where k3/k2 = 0.50 ± 0.10, 0.62 ± 0.20, 0.42 ± 0.06, and 0.24 ± 0.03 torr, and that k2a/k2 = 1.0, 1.0, 0.64 ± 0.04, and 0.56 ± 0.03, respectively, for C2H5ONO, n-C3H7ONO, n-C4H9ONO, and i-C4H9ONO.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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