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  • Dioxygen trapping  (3)
  • Calculations, force-field  (2)
  • 1
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 217-224 
    ISSN: 0009-2940
    Schlagwort(e): Homoaromaticity ; Resonance energy ; Calculations, force-field ; Heats of hydrogenation ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Heats of Hydrogenation, IV.  -  Homoaromaticity in Norcaradiene and CycloheptatrieneBy comparison of the heats of hydrogenation of fixed norcaradienes with analogous cyclobutane derivatives and from the difference of experimental heats of formation with values calculated by force-field methods the homoaromatic stabilization of norcaradienes and cycloheptatrienes are calculated and compared with the equilibrium position of the respective valence isomers.
    Zusätzliches Material: 9 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 2499-2521 
    ISSN: 0009-2940
    Schlagwort(e): Calculations, force-field ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Resonance Energy Calculation; the MM2ERW Force Field*The additivity of the thermochemical conjugation energy in acyclic systems allows one to extend force-field calculations to conjugated π systems without embarking on quantum-mechanical methods. The approach fails with cyclic delocalized systems, where resonance effects become important. Here the method provides the reference value needed to calculate resonance energies.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1998 (1998), S. 961-967 
    ISSN: 1434-193X
    Schlagwort(e): Diradicals ; Dioxygen trapping ; Diradical well ; Heat of formation ; Ab initio calculations ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The observation of practically identical activation parameters for the Cope rearrangement 2 → 6 and its “frustrated” counterpart 1 → 5 indicates a two-step mechanism for the reaction 2 → 6. Direct proof of this interpretation comes from trapping experiments, which demonstrate the intermediate formation of the diradicals 5 and 9. From the temperature and oxygen dependences of the trapping rates, recombination barriers of ΔH≠ = 11.5 and 6.5 kcal · mol-1 have been derived for 5 → 1 and 9 → 6, respectively. These results agree well with ab initio calculations (CASPT2).
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1997 (1997), S. 1323-1327 
    ISSN: 0947-3440
    Schlagwort(e): Diradicals ; Dioxygen trapping ; Diradical well ; Supercritical fluids ; Radicals ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: From the O2-dependence of the trapping rate of 1,1-difluoro-2,3-diphenylcyclopropane in supercritical CO2 in the temperature range 110-180°C and the rates of its geometrical isomerization and racemization of the trans-isomer, the energy profile for the geometrical isomerization is derived. Assuming that 7 is a common intermediate, the temperature dependence of the ratio of the rates of isomerization/racemization leads to a lowering of 1.2 kcal · mol-1 for the activation energy for the disrotatory cyclization of the intermediate diradical compared to the conrotatory mode. The energy barriers associated with cyclization of the diradical amount to 2.1 and 0.9 kcal · mol-1, respectively.
    Zusätzliches Material: 7 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 2000 (2000), S. 1983-1986 
    ISSN: 1434-193X
    Schlagwort(e): Radicals ; Dioxygen trapping ; Radical reactions ; Singlet-triplet splitting ; Thermochemistry ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: ---From the oxygen and temperature dependence of the trapping rate of 7,7-difluorobenzocyclopropene (1) in the range 180-240 °C, the energy profile of the equilibrium 1 →←2 has been obtained. From the heat of hydrogenation of 1, its heat of formation is derived (ΔHof = +3.8 kcal·mol-1), as a result of which the heat of formation of the singlet state of the diradical 2 is estimated as 25.7 kcal·mol-1. Whereas the trapping experiments demonstrate unambiguously a triplet ground state for 2, only a lower limit for the singlet-triplet splitting (〉 6 kcal·mol-1) can be given.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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