Gas‐Phase Reaction of CeV2O7+ with C2H4: Activation of CC and CH Bonds |
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| Authors: | Dr. Jia‐Bi Ma Zhen Yuan Jing‐Heng Meng Qing‐Yu Liu Prof. Dr. Sheng‐Gui He |
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| Affiliation: | 1. The Institute for Chemical Physics, Key Laboratory of Cluster Science, School of Chemistry, Beijing Institute of Technology, 100081, Beijing (P.R. China);2. State Key Laboratory for Structural Chemistry of Unstable and Stable Species, Institute of Chemistry, Chinese Academy of Sciences, 100190 Beijing (P.R. China) |
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| Abstract: | The reactivity of metal oxide clusters toward hydrocarbon molecules can be changed, tuned, or controlled by doping. Cerium‐doped vanadium cluster cations CeV2O7+ are generated by laser ablation, mass‐selected by a quadrupole mass filter, and then reacted with C2H4 in a linear ion trap reactor. The reaction is characterized by a reflectron time‐of‐flight mass spectrometer. Three types of reaction channels are observed: 1) single oxygen‐atom transfer , 2) double oxygen‐atom transfer , and 3) C?C bond cleavage. This study provides the first bimetallic oxide cluster ion, CeV2O7+, which gives rise to C?C bond cleavage of ethene. Neither CexOy± nor VxOy± alone possess the necessary topological and electronic properties to bring about such a reaction. |
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| Keywords: | cluster compounds density functional calculations gas‐phase reactions mass spectrometry reaction mechanisms |
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