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Gas‐Phase Reaction of CeV 2 O 7 + with C 2 H 4 : Activation of CC and CH Bonds
Author(s) -
Ma JiaBi,
Yuan Zhen,
Meng JingHeng,
Liu QingYu,
He ShengGui
Publication year - 2014
Publication title -
chemphyschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.016
H-Index - 140
eISSN - 1439-7641
pISSN - 1439-4235
DOI - 10.1002/cphc.201402347
Subject(s) - chemistry , bond cleavage , oxide , mass spectrometry , reactivity (psychology) , molecule , crystallography , cluster (spacecraft) , analytical chemistry (journal) , inorganic chemistry , photochemistry , catalysis , organic chemistry , chromatography , computer science , programming language , medicine , alternative medicine , pathology
The reactivity of metal oxide clusters toward hydrocarbon molecules can be changed, tuned, or controlled by doping. Cerium‐doped vanadium cluster cations CeV 2 O 7 + are generated by laser ablation, mass‐selected by a quadrupole mass filter, and then reacted with C 2 H 4 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) CC bond cleavage. This study provides the first bimetallic oxide cluster ion, CeV 2 O 7 + , which gives rise to CC bond cleavage of ethene. Neither Ce x O y ± nor V x O y ± alone possess the necessary topological and electronic properties to bring about such a reaction.
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