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  • 1
    ISSN: 1572-9001
    Keywords: Antiaromaticity ; aromaticity ; enthalpy of formation ; imides ; organic thermochemistry ; phenalene derivatives
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract In order to understand the aromaticity of 1,8-naphthalimides, the enthalpies of combustion and sublimation of N-methyl-1,8-naphthalimide were determined. The numerical values are −6095.8 ± 3.5 and 109.7 ± 0.8 kJ · mol−1. The enthalpies of formation of condensed and gas phase N-methyl-1,8-naphthalimide are accordingly −306.1 ± 3.9 and −196.4 ± 4.0 kJ · mol−1. It is deduced that naphthalimides enjoy some 40 kJ · mol−1 of aromatic stabilization over that of the maleimides, shown to be nominally destabilized and modestly antiaromatic in our recently published thermochemical study.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Structural chemistry 7 (1996), S. 307-308 
    ISSN: 1572-9001
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1572-9001
    Keywords: Thermochemistry ; combustion calorimetry ; enthalpies of combustion, of sublimation, of formation ; dimethoxybenzoic acids ; additive relationship ; substituent effect
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The energy of combustion of 2,5-dimethoxybenzoic acid has been determined using a static bomb calorimeter. The vapor pressures of the compound have been measured over a 18 K temperature interval by the Knudsen effusion technique. Heat capacity measurements betweenT=270 K andT=338 K were carried out by DSC. From these experimental results the standard molar enthalpies of combustion, sublimation, and formation in the crystalline and gaseous state at the temperature 298.15 K have been derived. With this compound, the series of mono- and dimethoxy-benzoic acids have been completed. Theirδf H m o values were expressed by an additive relationship, taking into account the number of methoxy groups and the number of all 1,2 interactions: an accuracy of 3.3 kJ·mol−1 was achieved. In an alternative approach the substituent effect of the methoxy groups was evaluated within the framework of isodesmic reactions. The effect of disubstitution was referred to mono derivatives and the excess energy—the so-called buttressing effect—was evaluated (2–24 kJ· mol−1 for individual bis derivatives). These values were explained in terms of the conformation of the methoxy group around the Car-O bond.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1434-193X
    Keywords: Resonance ; Hindered resonance ; Steric hindrance ; Conformation analysis ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Substituent effects of the tert-butyl group in isomeric tert-butylbenzoic acids have been investigated on the basis of enthalpies of formation, gas-phase acidities, acidities in methanol and in dimethyl sulfoxide, and the IR spectra in tetrachloromethane. In contrast to 2-methylbenzoic acid, 2-tert-butylbenzoic acid must adopt a non-planar conformation, as is confirmed by its IR spectrum. Enhanced acidity in the gas phase has been found for all isomers and attributed to a pole-induced dipole interaction in the anion (polarizability effect); in the ortho isomer the steric inhibition of resonance is only responsible for a minor part of the observed effect. In solution, the electrostatic interaction is attenuated, but remains strong in the case of the ortho isomer.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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