Publication | Open Access
Hydrogen Bonding in the Gas-Phase: The Molecular Structures of 2-Hydroxybenzamide (C<sub>7</sub>H<sub>7</sub>NO<sub>2</sub>) and 2-Methoxybenzamide (C<sub>8</sub>H<sub>9</sub>NO<sub>2</sub>), Obtained by Gas-Phase Electron Diffraction and Theoretical Calculations
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2013
Year
EngineeringGas-phase Electron DiffractionOrganic ChemistryElectron DiffractionComputational ChemistryChemistrySpectra-structure CorrelationBiophysicsTheoretical CalculationsBiochemistryChemical BondStable ConformersHydrogenQuantum ChemistryHydrogen BondingMolecular ChemistryNatural SciencesHydrogen BondHydrogen-bonded LiquidIntramolecular Hydrogen Bonding
The structures of 2-hydroxybenzamide (C7H7NO2) and 2-methoxybenzamide (C8H9NO2) have been determined in the gas-phase by electron diffraction using results from quantum chemical calculations to inform restraints used on the structural parameters. Theoretical methods (HF and MP2/6-311+G(d,p)) predict four stable conformers for both 2-hydroxybenzamide and 2-methoxybenzamide. For both compounds, evidence for intramolecular hydrogen bonding is presented. In 2-hydroxybenzamide, the observed hydrogen bonded fragment is between the hydroxyl and carbonyl groups, while in 2-methoxybenzamide, the hydrogen bonded fragment is between one of the hydrogen atoms of the amide group and the methoxy oxygen atom.
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