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  • Artikel: DFG Deutsche Nationallizenzen  (14)
  • 1980-1984  (5)
  • 1975-1979  (9)
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  • Artikel: DFG Deutsche Nationallizenzen  (14)
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  • 1
    ISSN: 1520-4995
    Quelle: ACS Legacy Archives
    Thema: Biologie , Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Analytical chemistry 49 (1977), S. 13-17 
    ISSN: 1520-6882
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 88 (1984), S. 2812-2817 
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of organic chemistry 47 (1982), S. 5339-5353 
    ISSN: 1520-6904
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Environmental science & technology 17 (1983), S. 721-730 
    ISSN: 1520-5851
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Energietechnik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 10 (1978), S. 41-66 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Tertiary-amyl amine has been decomposed in single-pulse shock-tube experiments. Rate expressions for several of the important primary steps are \documentclass{article}\pagestyle{empty}\begin{document}$$ k(t{\rm C}_5 {\rm H}_{11 - {\rm NH}_2} \to t{\rm C}_5 {\rm H}_{11}\!\!\cdot + {\rm NH}_2\cdot) = 10^{15.9} \exp (-39,700/T)\sec ^{- 1} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k({\rm C}_2 {\rm H}_5- {\rm C}({\rm CH}_3)_2{\rm NH}_2 \to {\rm C}_2 {\rm H}_5 \cdot + \cdot{\rm C}({\rm CH}_3)_2{\rm NH}_2) = 10^{16.5} \exp (- 38,500/T)\sec ^{- 1} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k(t{\rm C}_5 {\rm H}_{11} {\rm NH}_2 \to {\rm C}_5 {\rm H}_{10} + {\rm NH}_3) 〈10^{14.5} \exp (- 37,200/T)\sec ^{- 1} $$\end{document}This leads to D(CH3—H) - D(NH2—H) = -10.5 kJ and D[(CH3)3C—H] - D[(CH3)2NH2C—H] = + 6 kJ.The present and earlier comparative rate single-pulse shock-tube data when combined with high-pressure hydrazine decomposition results-(after correcting for fall off effects through RRKM calculations) gives \documentclass{article}\pagestyle{empty}\begin{document}$$ [k_r^2 (t{\rm C}_5 {\rm H}_{11} \cdot,{\rm NH}_2 \cdot)/k_r (t{\rm C}_5 {\rm H}_{11} \cdot,t{\rm C}_5 {\rm H}_{11} \cdot)k_r ({\rm NH}_2 \cdot,{\rm NH}_2 \cdot)]^{1/2} \sim 2\,{\rm at}\,1100^o {\rm K} $$\end{document} where kr(…) is the recombination rate involving the appropriate radicals. This suggests that in this context amino radical behavior is analogous to that of alkyl radicals. If this agreement is exact, then \documentclass{article}\pagestyle{empty}\begin{document}$$ k_\infty ({\rm N}_2 {\rm H}_4 \to 2{\rm NH}_2 \cdot) = 10^{16.25} \exp (- 32,300/T)\sec ^{- 1} $$\end{document} Rate expressions for the primary step in the decomposition of a variety of primary amines have been computed. In the case of benzyl amine where data exist the agreement is satisfactory. The following differences in bond energies have been estimated: \documentclass{article}\pagestyle{empty}\begin{document}$$ D(i{\rm C}_3 {\rm H}_7 {-\!-} {\rm H}) {-\!-} D[{\rm CH}_3 ({\rm NH}_2){\rm CH} {-\!-} {\rm H}] = 14.3\,{\rm kJ} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ D({\rm C}_2 {\rm H}_5 {-\!-} {\rm H}) - D({\rm NH}_2 {\rm CH}_2 {-\!-} {\rm H}) = 15.9\,{\rm kJ} $$\end{document}
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 8 (1976), S. 193-203 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The life times of chemically activated alcohols have been determined using the high-pressure unimolecular rate parameters for thermal decomposition of alcohols from shocktube studies and RRKM calculations. They are compared with literature numbers (from insertion of 0(1D) into hydrocarbons). It is suggested that in some cases singlet oxygen carries excess energy into the hydrocarbon. The consequences of such an assumption are explored and discrepancies with previously published conclusions discussed.
    Zusätzliches Material: 4 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 10 (1978), S. 1119-1138 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The mechanism and initial rates of decomposition of cyclohexane and 1-hexene have been determined from single-pulse shock-tube experiments. The main initial processes involve isomerization of cyclohexane to 1-hexene, followed by decomposition of 1-hexene. From comparative rate experiments the following rate expressions have been derived: \documentclass{article}\pagestyle{empty}\begin{document}$$ k({\rm cyclohexane} \to 1 - {\rm hexene}) = 10^{16.7} \exp (- 44,400/T)\,\,\sec ^{- 1} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k_B (1 - {\rm hexene} \to {\rm C}_{\rm 3} {\rm H}_{{\rm 5}} \cdot {\rm + nC}_{\rm 3} {\rm H}_{{\rm 7}} \cdot) = 10^{15.9} \exp (- 35,600/T)\,\,\sec ^{- 1} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k_{\rm M} (1 - {\rm hexene} \to 2{\rm C}_{\rm 3} {\rm H}_6) = 10^{12.6} \exp (- 28,900/T)\,\,\sec ^{- 1} $$\end{document} The 1-hexene bond-braking reaction leads to an allylic resonance energy of 42.7 kJ and a heat of formation of allyl radicals of 176.6 kJ (300°K). There appear to be general relations relating the rate expressions for the decomposition of alkynes, alkanes, and alkenes. Studies on the induced decomposition of cyclohexane have also been carried out.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 16 (1984), S. 1543-1556 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 5-Methyl-hexanone-2, 3-methyl-pentanone-2, and hexanone-2 have been decomposed in comparative rate single pulse shock tube experiments. The mechanism of decomposition involves the breaking of carbon-carbon bonds as well as molecular processes involving 6-center complexes. The following rate expressions at 1100 K have been obtained: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{rcl} k(3{\rm - methyl - pentanone - 2} \to {\rm CH}_{\rm 3} {\rm \dot CO} + {\rm sC}_4 {\rm H}_9 .) = 10^{16.4} \exp (- 38,300/T)/{\rm s} \\ k(5{\rm - methyl - hexanone - 2} \to {\rm CH}_{\rm 3} {\rm \dot CO} + {\rm iC}_4 {\rm H}_9 .) = 10^{16.6} \exp (- 40,600/T)/{\rm s} \\ k(5{\rm - methyl - hexanone - 2} \to {\rm CH}_{\rm 3} {\rm COCH}_{\rm 3} + {\rm iC}_4 {\rm H}_8) = 10^{12.56} \exp (- 31,600/T)/{\rm s} \\ k({\rm hexanone - 2} \to {\rm CH}_{\rm 3} {\rm COCH}_{\rm 3} + {\rm C}_3 {\rm H}_6) = 10^{13.28} \exp (- 32,400/T)/{\rm s} \\ \end{array} $$\end{document} These results lead to ΔHf(CH3ĊO) = - 13.8 kJ and ΔHf(CH3COCH2·) = - 12.6 kJ at 300 K. They are compared with existing literature values and some generalizations are made with regard to the stability of carbonyl compounds.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 10 (1978), S. 599-617 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Cyclopentane has been decomposed in comparative-rate single-pulse shock-tube experiments. The pyrolytic mechanism involves isomerization to 1-pentene and also a minor pathway leading to cyclopropane and ethylene. This is followed by the decomposition of 1-pentene and cyclopropane. The rate expressions over the temperature range of 1000°-1200° K are \documentclass{article}\pagestyle{empty}\begin{document}$$ k(c-{\rm C}_{\rm 5} {\rm H}_{{\rm 10}} \to 1-{\rm C}_{\rm 5} {\rm H}_{{\rm 10}}) = 10^{16.1} \exp (- 42,700/T)\sec ^{- 1} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k(c-{\rm C}_{\rm 5} {\rm H}_{\rm 10} \to (c-{\rm C}_{\rm 3} {\rm H}_{\rm 6} + {\rm C}_{\rm 2} {\rm H}_{\rm 4}) = 10^{16.25} \exp (- 47,840/T)\sec ^{- 1} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k(1 - {\rm pentene} \to {\rm C}_{\rm 3} {\rm H}_{\rm 6} + {\rm C}_{\rm 2} {\rm H}_{\rm 5}) \sim 10^{16} \exp (- 35,900/T)\sec ^{- 1} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k(1 - {\rm pentene} \to {\rm C}_{\rm 3} {\rm H}_{\rm 6} + {\rm C}_{\rm 2} {\rm H}_{\rm 4}) \sim 10^{12.5} \exp (- 28,900/T)\sec ^{- 1} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k(c-{\rm C}_{\rm 3} {\rm H}_{\rm 6} \to {\rm C}_{\rm 3} {\rm H}_{\rm 6}) = 10^{14.3} \exp (- 31,100/T)\sec ^{- 1} {\rm at}\ {\rm 5}\ {\rm atm} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k(c-{\rm C}_{\rm 3} {\rm H}_{\rm 6} \to {\rm C}_{\rm 3} {\rm H}_{\rm 6}) = 10^{14.1} \exp (- 31,100/T)\sec ^{- 1} {\rm at}\ {\rm 1.7}\ {\rm atm} $$\end{document}Details of the cyclopentane decomposition processes are considered, and it appears that if the trimethylene radical is an intermediate, then ΔHf(trimethylene) ≤ 280 kJ/mol at 300°K.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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