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  • 1975-1979
  • 1970-1974  (9)
  • 1972  (9)
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Years
  • 1975-1979
  • 1970-1974  (9)
Year
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 94 (1972), S. 4856-4864 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 94 (1972), S. 4864-4871 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    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〉 76 (1972), S. 1416-1419 
    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〉 76 (1972), S. 1919-1924 
    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〉 76 (1972), S. 2659-2665 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 4 (1972), S. 417-432 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The room-temperature photolysis of N2O (10-100 torr) at 2139 Å to produce O(1D) has been studied in the presence of CH4 (10-891 torr). The reactions of O(1D) with CH4 were found to be \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{*{20}c} {(4)} & {{\rm O(}^{\rm 1} D{\rm)} + {\rm CH}_{\rm 4} } & \to & {{\rm HO + CH}_{\rm 3} } & {0.95 \pm 0.05} \\ {(8)} & {} & \to & {{\rm O(}^{\rm 3} P{\rm)} + {\rm CH}_{\rm 4} } & {{\rm 0}{\rm .05} \pm {\rm 0}{\rm .05}} \\ {} & {} & \to & {{\rm CH}_{\rm 2} + {\rm H}_{\rm 2} {\rm O}} & {{\rm 〈 0}{\rm .03}} \\ {} & {} & \to & {{\rm CH}_{\rm 3} {\rm OH}} & {{\rm 〈 0}{\rm .01}} \\ {} & {} & \to & {{\rm CH}_{\rm 2} {\rm O + H}_{\rm 2}} & {{\rm 〈 0}{\rm .002}} \\\end{array}$$\end{document} The method of chemical difference was used to measure the rate constant ratio k4/(k2 + k3), where reactions (2) and (3) are \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{*{20}c} {(2)} & {{\rm O(}^{\rm 1} D{\rm)} + {\rm N}_{\rm 2} {\rm O}} & { \to {\rm N}_{\rm 2} + {\rm O}_{\rm 2} } \\ {(3)} & {} & { \to 2{\rm NO}} \\\end{array}$$\end{document} The CH3 radicals produced in reaction (4) react with the O2 and NO produced in reactions (2) and (3). Thus, near the endpoint of the internal titration, φ{C2H6} gives an accurate measure of k4/(k2 + k3). For the translationally energetic O(1D) atoms produced in the photolysis, k4/(k2 + k3) = 2.28 ± 0.20. However, if He is added to remove the excess translational energy, then k4/(k2 + k3) drops to 1.35 ± 0.3.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 4 (1972), S. 529-540 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: NO2 was photolyzed with 2288 Å radiation at 300° and 423°K in the presence of H2O, CO, and in some cases excess He. The photolysis produces O(1D) atoms which react with H2O to give HO radicals \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{*{20}c} {{\rm (3)}} & {{\rm O(}^{\rm 1} D{\rm)} + {\rm H}_{\rm 2} {\rm O} \to 2{\rm HO}} \\\end{array}$$\end{document} or are deactivated by CO to O(3P) atoms \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{*{20}c} {{\rm (5)}} & {{\rm O(}^{\rm 1} D{\rm)} + {\rm CO} \to {\rm O(}^{\rm 3} P{\rm) + CO}} \\\end{array}$$\end{document} The ratio k5/k3 is temperature dependent, being 0.33 at 300°K and 0.60 at 423°K. From these two points, the Arrhenius expression is estimated to be k5/k3 = 2.6 exp(-1200/RT) where R is in cal/mole - °K. The OH radical is either removed by NO2 \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{*{20}c} {{\rm (1)}} & {{\rm OH} + {\rm NO}_{\rm 2} {\rm (+M)} \to {\rm HNO}_{\rm 3} {\rm (+M)}} \\\end{array}$$\end{document} or reacts with CO \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{*{20}c} {{\rm (2)}} & {{\rm OH} + {\rm CO} \to {\rm H} + {\rm CO}_{\rm 2} } \\\end{array}$$\end{document} The ratio k2/kα is 0.019 at 300°K and 0.027 at 423°K, and the ratio k2/k0 is 1.65 × 10-5M at 300°K and 2.84 × 10-5M at 423°K, with H2O as the chaperone gas, where kα = k1 in the high-pressure limit and k0[M] = k1 in the low-pressure limit. When combined with the value of k2 = 4.2 × 108 exp(-1100/RT) M-1sec-1, kα = 6.3 × 109 exp (-340/RT)M-1sec-1 and k0 = 4.0 × 1012M-2sec-1, independent of temperature for H2O as the chaperone gas. He is about 1/8 as efficient as H2O.
    Additional Material: 3 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 4 (1972), S. 497-512 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The method of chemical difference was utilized to accurately determine the relative importance of all the reaction steps in the direct photolysis of N2O at 2139 Å (25° and 250°C) and 1849 Å (25° C), as well as in the Hg6(1P1)-sensitized photolysis of N2O at 1849 Å (25°C). In all cases, the primary process is predominantly, if not exclusively, \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{*{20}c} {{\rm (1)}} & {{\rm N}_{\rm 2} {\rm O} + hv{\rm or H}_{\rm g} 6(^1 P_1) \to {\rm N}_{\rm 2} + {\rm O(}^{\rm 1} D{\rm)}} \\\end{array}$$\end{document} Experiments with trace amounts of C3H6 added showed a slight, but not significant, difference in product ratios (N2 and O2). From these experiments the quantum yield of O(3P) from all possible sources was estimated as 0.02 ± 0.02. Experiments with excess N2 at 1849 Å indicated that O(1S) was not produced in the direct photolysis. The O(1S) yield is probably zero, and certainly 〈0.05. The O(1D) atom can react with N2O via \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{l} \begin{array}{*{20}c} {{\rm (2)}} & {{\rm O(}^{\rm 1} D{\rm)} + {\rm N}_{\rm 2} {\rm O} \to {\rm N}_{\rm 2} + {\rm O}_2 } \\\end{array} \\ \begin{array}{*{20}c} {{\rm (3)}} & {{\rm O(}^{\rm 1} D{\rm)} + {\rm N}_{\rm 2} {\rm O} \to 2{\rm NO}} \\\end{array} \\ \end{array}$$\end{document} The ratio k2/k3 was found to be 0.69 ± 0.05 in all cases. When combined with other data from our laboratory, the average value is 0.65 ± 0.07. This represents the value for translationally energetic O(1D) atoms. When excess He was added to remove the excess translational energy, k2/k3 rose to 0.83 ± 0.06, which is in reasonable agreement with the value of 1.01 ± 0.06 found in another laboratory. We conclude that for O(1D) atoms with no excess thermal energy, k2/k3 = 0.90 ± 0.10.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 4 (1972), S. 575-589 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of NO2 with C2F4 was studied at 30°, 68°, 114°, and 157°C by in situ monitoring the infrared absorption bands of the products. The major primary products of the reaction are O2NCF2CFO and FNO. Smaller amounts of CF2O (and presumably NO) are also produced. There was no evidence for other primary products, though they may have been produced in minor amounts. The rate laws for the production of both O2NCF2CFO and CF2O are first order in both [NO2] and [C2F4]. CF2O production is at least partly heterogeneous as demonstrated by packing the quartz reaction vessel with Pyrex beads and by using a Monel cell. The homogeneous rate constant obtained from the high-temperature results gives a rate constant of 3.4 × 108 exp (minus;17000/RT) M-1sec-1 for CF2O production. Actually these Arrhenius parameters represent lower limits, since the heterogeneous reaction may still be playing a significant role. The production rate of O2NCF2CFO is not much affected by changing the nature of the surface or the surface to volume ratio. However the reaction may be heterogeneous, since the rate constant for its formation of 1.3 × 104 e×p (-7500/RT) M-1sec-1 has an abnormally low pree×ponential factor. E×periments in the presence of NO indicate that the mechanism for O2NCF2CFO formatlon is \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{l} \begin{array}{*{20}c} {(11)} & {{\rm NO}_{\rm 2} + {\rm C}_{\rm 2} {\rm F}_{\rm 4} \to {\rm O}_{\rm 2} {\rm NCF}_{\rm 2} {\rm CF}_{\rm 2} } \\ \end{array} \\ \begin{array}{*{20}c} {(12)} & {{\rm O}_{\rm 2} + {\rm NCF}_{\rm 2} {\rm CF}_{\rm 2} + {\rm NO}_{\rm 2} \to {\rm O}_{\rm 2} {\rm NCF}_{\rm 2} {\rm CFO} + {\rm FNO}} \\ \end{array} \\ \end{array}$$\end{document} The intermediate can also react with NO: \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{*{20}c} {(13)} & {{\rm O}_{\rm 2} {\rm NCF}_{\rm 2} {\rm CF}_{\rm 2} + {\rm NO} \to {\rm O}_{\rm 2} {\rm NCF}_{\rm 2} {\rm CF}_{\rm 2} {\rm NO}} \\ \end{array}$$\end{document} with k13/k12 = 1.3.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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