The ionization effects on 28 conformations of N-glycylglycine are analyzed by means of the hybrid B3LYP and the hybrid meta-MPWB1K density functionals and by single-point calculations at the CCSD(T) level of theory. The most favorable process observed corresponds to the ionization of the only neutral conformation that presents a OH⋯NH2 intramolecular hydrogen bond, which leads to CO2 elimination after a spontaneous proton transfer from –COOH to NH2. The remaining neutral structures evolve to 20 different conformations of N-glycylglycine radical cation, which lie about 25–40kcal∕mol higher than the decarboxylated [NH3CH2CONHCH2]+̇⋯[CO2] complex. Structural changes induced by ionization depend on the intramolecular hydrogen bonds of the initial conformation, since they determine the nature of the electron hole formed. In most cases, ionization takes place at the terminal –NH2 and –CO of the amide bond, which produces a strengthening of the peptide bond and the formation of new –NH2⋯OCamide and –NH2⋯OCOH hydrogen bonds. However, if –NH2 and –COamide simultaneously act as proton acceptor in the neutral conformation, ionization is mainly localized at the carboxylic group, which produces a strengthening of the –COOH⋯OCamide bond. Both functionals lead to similar trends and compare well with CCSD(T) results except for a few cases for which B3LYP provides a too delocalized picture of the electron hole and consequently leads to artificial geometry reorganization.
The ionization effects on 28 conformations of N-glycylglycine are analyzed by means of the hybrid B3LYP and the hybrid meta-MPWB1K density functionals and by single-point calculations at the CCSD(T) level of theory. The most favorable process observed corresponds to the ionization of the only neutral conformation that presents a OH⋯NH2 intramolecular hydrogen bond, which leads to CO2 elimination after a spontaneous proton transfer from –COOH to NH2. The remaining neutral structures evolve to 20 different conformations of N-glycylglycine radical cation, which lie about 25–40kcal∕mol higher than the decarboxylated [NH3CH2CONHCH2]+̇⋯[CO2] complex. Structural changes induced by ionization depend on the intramolecular hydrogen bonds of the initial conformation, since they determine the nature of the electron hole formed. In most cases, ionization takes place at the terminal –NH2 and –CO of the amide bond, which produces a strengthening of the peptide bond and the formation of new –NH2⋯OCamide and –NH2⋯OCOH hydrogen bonds. However, if –NH2 and –COamide simultaneously act as proton acceptor in the neutral conformation, ionization is mainly localized at the carboxylic group, which produces a strengthening of the –COOH⋯OCamide bond. Both functionals lead to similar trends and compare well with CCSD(T) results except for a few cases for which B3LYP provides a too delocalized picture of the electron hole and consequently leads to artificial geometry reorganization.