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Title: THEORETICAL CHARACTERIZATION OF FREE N-(METHOXYCARBONYL)GLYCINE AND ITS INTERACTION WITH WATER
Authors: Nguyen, Minh Tho ×
DEWAEL, K
ZEEGERSHUYSKENS, T #
Issue Date: 1995
Publisher: AMER CHEMICAL SOC
Series Title: Journal of physical chemistry vol:99 issue:24 pages:9739-9746
Conference: date:CATHOLIC UNIV LEUVEN,DEPT CHEM,B-3001 HEVERLEE,BELGIUM
Abstract: N-(methoxycarbonyl)glycine (NMG) has been characterized by ab initio molecular orbital methods. HF/6-31G* geometry optimizations have been performed to mimic the C-5 and C-7 conformations of model dipeptides. The C-7 conformation is characterized by an intramolecular hydrogen bond between the OH group and the oxygen atom of the methane function. In the C-5 conformation, the NH group is not involved in an intramolecular hydrogen bond and the nitrogen atom is more pyramidal than in the dipeptides (pseudo C-5 conformation). The C-7 conformer is about 8 kJ . mol(-1) higher in energy than the C-5 conformer (MP2/6-31G**). The differences between the normal modes of the two conformers and their OD and ND isotopomers are discussed. Interaction of NMG with a water molecule induces only small changes in geometry. The most stable structure is obtained for a cyclic COOH ... OH2 system with a shorter O-W ... HO and a longer OWHW ... O=C hydrogen bond. A second stable monohydrate is obtained for a cyclic structure involving the NH bond and the carboxylic oxygen atom. The energies of association are about -41 and -33 kJ . mol(-1), respectively. These results are discussed as a function of the experimental gas-phase acidities of biological NH and COOH proton donors. Some infrared shifts induced by the association with water are discussed. A linear relationship is found between computed frequency shifts of the OH stretching mode and the elongations of the corresponding bond. This relation is very similar to the empirical correlation for OH ... O hydrogen bonded systems in the solid state.
ISSN: 0022-3654
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Quantum Chemistry and Physical Chemistry Section
× corresponding author
# (joint) last author

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