TY - JOUR
T1 - Reactions of V4O10+ cluster ions with simple inorganic and organic molecules
AU - Yuan, Zhen
AU - Zhao, Yan Xia
AU - Li, Xiao Na
AU - He, Sheng Gui
PY - 2013
Y1 - 2013
N2 - The reactivity of mass-selected V4O10+ cluster ions toward hydrocarbon molecules including CH4, C 2H4, and C2H6 was explored in the references case by case. Herein, further systematic studies on the reactions of V4O10+ with simple inorganic and organic molecules (H2, CO, CH4, C2H2, C 2H4, and C2H6) are presented. The vanadium oxide cluster ions are prepared by laser ablation and the V 4O10+ clusters are selected by a quadrupole mass filter and interacted with the simple molecules in a hexapole reaction cell. The reactant and product ions are detected by a reflectron time-of-flight mass spectrometer. Hydrogen and oxygen atom transfer reactions are observed. Density functional theory calculations are carried out for the reaction mechanism of V4O10+ + H2. The oxygen atom transfer (OAT) channel V4O10+ + H 2 → V4O9+ + H2O is much more exothermic than the hydrogen atom transfer (HAT) channel V 4O10+ + H2 → V 4O10H+ + H whereas the former is less favorable than the later in terms of the reaction kinetics. The computational result is in good agreement with the experiment that the HAT (H2 splitting) rather than the OAT (water formation) is observed for V4O 10+ + H2.
AB - The reactivity of mass-selected V4O10+ cluster ions toward hydrocarbon molecules including CH4, C 2H4, and C2H6 was explored in the references case by case. Herein, further systematic studies on the reactions of V4O10+ with simple inorganic and organic molecules (H2, CO, CH4, C2H2, C 2H4, and C2H6) are presented. The vanadium oxide cluster ions are prepared by laser ablation and the V 4O10+ clusters are selected by a quadrupole mass filter and interacted with the simple molecules in a hexapole reaction cell. The reactant and product ions are detected by a reflectron time-of-flight mass spectrometer. Hydrogen and oxygen atom transfer reactions are observed. Density functional theory calculations are carried out for the reaction mechanism of V4O10+ + H2. The oxygen atom transfer (OAT) channel V4O10+ + H 2 → V4O9+ + H2O is much more exothermic than the hydrogen atom transfer (HAT) channel V 4O10+ + H2 → V 4O10H+ + H whereas the former is less favorable than the later in terms of the reaction kinetics. The computational result is in good agreement with the experiment that the HAT (H2 splitting) rather than the OAT (water formation) is observed for V4O 10+ + H2.
KW - Density functional computations
KW - Hydrogen atom transfer
KW - Mass spectrometry
KW - Oxygen-centered radicals
KW - Reaction mechanisms
KW - Vanadium oxide
UR - http://www.scopus.com/inward/record.url?scp=84888298766&partnerID=8YFLogxK
U2 - 10.1016/j.ijms.2013.06.004
DO - 10.1016/j.ijms.2013.06.004
M3 - Article
AN - SCOPUS:84888298766
SN - 1387-3806
VL - 354-355
SP - 105
EP - 112
JO - International Journal of Mass Spectrometry
JF - International Journal of Mass Spectrometry
ER -