Proton Migration in Clusters Consisting of Protonated Pyridine Solvated by Water Molecules

被引:11
作者
Berthias, Francis [1 ]
Feketeova, Linda [1 ]
Chermette, Henry [2 ]
Forquet, Valerian [2 ]
Morell, Christophe [2 ]
Abdoul-Carime, Hassan [1 ]
Farizon, Bernadette [1 ]
Farizon, Michel [1 ]
Maerk, Tilmann D. [3 ]
机构
[1] Univ Lyon 1, Inst Phys Nucl Lyon, CNRS, IN2P3 UMR 5822, F-69622 Villeurbanne, France
[2] Univ Lyon 1, Inst Sci Analyt, CNRS UMR 5280, F-69622 Villeurbanne, France
[3] Leopold Franzens Univ Innsbruck, Inst Ionenphys & Angew Phys, A-6020 Innsbruck, Austria
关键词
biomolecular clusters; density functional calculations; mass spectrometry; protonated pyridine-water clusters; proton transfer; GAS-PHASE; ENERGY; AFFINITIES; MULTIPHOTON; IONIZATION; IONS;
D O I
10.1002/cphc.201500465
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Proton transfer (PT) from protonated pyridine to water molecules is observed after excitation of microhydrated protonated pyridine (Py) clusters PyH+(H2O)(n) (n=0-5) is induced by a single collision with an Ar atom at high incident velocity (95x10(3)ms(-1)). Besides the fragmentation channel associated with the evaporation of water molecules, the charged-fragment mass spectrum shows competition between the production of the PyH+ ion (or its corresponding charged fragments) and the production of H+(H2O) or H+(H2O)(2) ions. The increase in the production of protonated water fragments as a function of the number of H2O molecules in the parent cluster ion as well sd the observation of a stable H+(H2O)(2) fragment, even in the case of the dissociation of PyH+(H2O)(2), are evidence of the crucial role of PT in the relaxation process, even for a small number of solvating water molecules.
引用
收藏
页码:3151 / 3155
页数:5
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