Abstract
Using a wide panel of quantum mechanical approaches, we have computed the structures and properties of protonated glycine-water complexes. It turns out that (1) MP2 is the minimum theoretical level to get accurate hydration energies; (2) anharmonicity strongly influences the vibrational spectra but has no impact on the complexation energy; (3) the correction of basis set superposition error significantly modifies both the energetic and entropic terms; and (4) 6-31+G(d) is the necessary minimal basis set. Using our best level of theory, we have obtained theoretical hydration enthalpies that are in perfect agreement with the most recent experimental investigations.
Original language | English |
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Pages (from-to) | 57-61 |
Number of pages | 5 |
Journal | Chemical Physics Letters |
Volume | 445 |
Issue number | 1-3 |
DOIs | |
Publication status | Published - 4 Sept 2007 |