The thermochemistry of gas-phase ion molecule interactions and the structures of various clusters between protonated glycine (GlyH+), glycine, and ammonia have been studied by high pressure mass spectrometry (HP-MS) and ab initio calculations. For the association reactions of GlyH+ with NH3, Gly(NH3)H+ with NH3, and (Gly)2H+ with NH3, the enthalpy changes experimentally determined are 23.2, 18.3, and 19.1 kcal mol1 (1 cal = 4.184 J), respectively. For all clusters investigated, the measured binding enthalpies are in excellent agreement with those obtained from ab initio calculations at the B3LYP/6-311+G(d,p) level of theory. Different isomers of each of these clusters have been obtained and the corresponding binding energies have been computed. The potential energy surface for isomerization of the clusters of protonated glycine with ammonia has also been computed at the same level. For this cluster, the three most stable isomers all involve a proton transfer from protonated glycine to ammonia. According to the calculated potential energy surface, the barrier between GN4, the least stable isomer, and the most stable isomer (GN1) is 11.5 kcal mol1 at 298 K. Thus, this isomerization will be facile given the exothermicity of the association reaction. Therefore, a statistical distribution of isomers will be present under thermal equilibrium conditions. Single point energy calculations at the MP2(full)/6-311++G(2d,2p)//B3LYP/6-311+G(d,p) level of theory reveal that the isomer GN2 in which glycine has a zwitterionic structure has the same energy as the most stable non-zwitterionic isomer GN1. NH4+ evidently may stabilize the zwitterionic structure of glycine. In contrast, N2H7+ and GlyH+ are not as effective in stabilizing the zwitterionic structure of glycine. This likely results from the more localized charge in NH4+ giving rise to stronger hydrogen bonds with the carboxylate moiety of zwitterionic glycine. This conjecture is supported by the computational results.Key words: high pressure mass spectrometry, glycine, gas-phase ion thermochemistry, ab initio calculations, cluster structure.
Reaction Roulette: Utilizing Elemental MS/MS for the Characterization of Gas Phase Ion-Molecule Interactions
