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- Title
Effect of stepwise microhydration on the methylammonium···phenol and ammonium···phenol interaction.
- Authors
Rodríguez-Sanz, Ana; Carrazana-García, J.; Cabaleiro-Lago, Enrique; Rodríguez-Otero, Jesús
- Abstract
A computational study has been performed for studying the characteristics of the interaction of phenol with ammonium and methylammonium cations. The effect of the presence of water molecules has also been considered by microhydrating the clusters with up to three water molecules. Clusters of phenol with ammonium and methylammonium cations present similar characteristics, though ammonium complexes have been found to be more stable than the methylammonium ones. The first water molecule included in the complexes interacts with a N-H group of ammoniun cations and simultaneously with the hydroxyl oxygen atom of phenol (or the aromatic ring). This first water molecule is more tightly bound in the complex, so the stability gain as more water molecules are included drops significantly by 2-3 kcal mol with respect to the first one. As more water molecules are included, the differences between favorable coordination sites (the cation, the hydroxyl group or a previous water molecule) decrease. As a consequence, several of the most stable complexes located including three water molecules already exhibit hydrogen bonds between the hydroxyl group and one water molecule. The results indicate that a cyclic pattern formed by a series of hydrogen bonds: π···H-N-H···O-H···O-ϕ, is characteristic of the most stable minima, being kept as more water molecules are included in the system. Therefore, this pattern can be expected to be crucial in ammonium cations···phenol interaction if exposed to the solvent to any degree.
- Subjects
METHYLAMMONIUM; HYDRATION; PHENOLS; ORGANIC solvents; HYDROGEN bonding; HYDROXYL group
- Publication
Journal of Molecular Modeling, 2013, Vol 19, Issue 5, p1985
- ISSN
1610-2940
- Publication type
Article
- DOI
10.1007/s00894-012-1579-9