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Proton and sodium ion affinities of glycine and its sodium salt in the gas phase. Ab initio calculations
Author(s) -
Bouchonnet S.,
Hoppilliard Y.
Publication year - 1992
Publication title -
organic mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.475
H-Index - 121
eISSN - 1096-9888
pISSN - 0030-493X
DOI - 10.1002/oms.1210270202
Subject(s) - protonation , proton affinity , affinities , chemistry , ab initio , proton , ion , crystallography , glycine , ab initio quantum chemistry methods , ring (chemistry) , computational chemistry , sodium , gas phase , stereochemistry , molecule , amino acid , organic chemistry , biochemistry , physics , quantum mechanics
The energies of protonation and Na + cationization of glycine (GLY) and its (GLY − H + Na) salt in the gas phase were calculated using ab inltio calculations. The proton affinity of GLY, valued at the MP2/6–31G*//3‐21G level, is 937 kJ mol −1 . The amino function is confirmed to be the most favourable site of protonation: ‘proton affinities’ of the carbonyl and hydroxyl functions are calculated to be 75 and 180 kJ mol −1 , respectively, lower than that of NH 2 at the MP2/6‐31G*//3–21G level. Calculations performed up to the MP2/6–31G*//3–21G level give the Na + affinity of GLY as 189 kJ mol −1 and the H + and Na + affinities of (GLY – H + Na) as 1079 and 298 kJ mol −1 , respectively. The geometries of all neutral and protonated species optimized with the 3–21G basis set are described. Both H* and Na + cations complex preferably between the nitrogen atom and the carbonyl oxygen atom, leading to pseudo‐five‐membered ring structures in which NaO and NaN bonds lengths are greater than 2 Å.