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The Elusive Antiaromaticity of Maleimides and Maleic Anhydride: Enthalpies of Formation of <i>N</i>-Methylmaleimide, <i>N</i>-Methylsuccinimide, <i>N</i>-Methylphthalimide, and <i>N</i>-Benzoyl-<i>N</i>-methylbenzamide
58
Citations
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References
1997
Year
EngineeringOrganic ChemistryNumerical ValuesExperimental ThermodynamicsComputational ChemistryChemistryPharmaceutical ChemistryGaseous StateSolid StateElusive AntiaromaticityThermoanalytical MethodMaterials ScienceDerivative (Chemistry)Chemical ThermodynamicsBiochemistryMaleic AnhydridePhysical ChemistryQuantum ChemistryPharmacologyNatural SciencesChemical KineticsSynthetic Chemistry
In order to understand the antiaromaticity of maleimides, the enthalpies of formation and sublimation of N-methylmaleimide, N-methylsuccinimide, N-methylphthalimide, and N-benzoyl-N-methylbenzamide were measured. The numerical values of enthalpies of formation for these compounds in the solid state are -329.3 +/- 1.4, -469.8 +/- 1.6, -325.0 +/- 2.1, and -239.6 +/- 3.8 kJ mol(-)(1), respectively, while the corresponding values in the gaseous state are -256.0 +/- 1.5, -389.7 +/- 1.6, -233.9 +/- 2.2, and -119.5 +/- 3.8 kJ mol(-)(1), respectively. The values of enthalpies of sublimation for the same compounds are 73.3 +/- 0.5, 80.1 +/- 0.3, 91.1 +/- 0.5, and 120.1 +/- 0.4 kJ mol(-)(1), respectively. We find that the antiaromaticity of maleimides is only modest.
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