Hydrogen Bonding in the Gas-Phase – The Molecular Structures of 2-Hydroxybenzamide (C7H7NO2) and 2-Methoxybenzamide (C8H9NO2), obtained by Gas-Phase Electron Diffraction and Theoretical Calculations.
Journal article, Peer reviewed
Postprint version of published article
Åpne
Permanent lenke
https://hdl.handle.net/10642/2039Utgivelsesdato
2013-03-13Metadata
Vis full innførselSamlinger
Originalversjon
Aarset, K., Page, E. M., & Rice, D. A. (2013). Hydrogen Bonding in the Gas-Phase: The Molecular Structures of 2-Hydroxybenzamide (C7H7NO2) and 2-Methoxybenzamide (C8H9NO2), Obtained by Gas-Phase Electron Diffraction and Theoretical Calculations. The Journal of Physical Chemistry A, 117(14), 3034-3040. http://dx.doi.org/10.1021/jp311003dSammendrag
The structures of 2-hydroxybenzamide (C
7
H
7
NO
2
) and 2-methoxybenzamide (C
8
H
9
NO
2) 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.