Reactions of Group V Transition Metal Oxide Cluster Ions with Ethane and Ethylene

作者
K. A. Zemski,Dina R. Justes,A. Welford Castleman
出处
期刊:Journal of Physical Chemistry A [American Chemical Society]
卷期号:105 (45): 10237-10245 被引量:116
标识
DOI:10.1021/jp012319r
摘要

Reactions of mass-selected group V transition metal oxide cluster ions (V x O y ±, Nb x O y ±, and Ta x O y ± ) with ethane (C 2 H 6 ) and ethylene (C 2 H 4 ) were investigated. The major reaction channels observed during the reactions of C 2 hydrocarbons with M x O y + were association and oxygen transfer. The association channel, M x O y C 2 H n +, where n = 4 or 6, was common to most of the group V transition metal oxide cluster cations examined. However, a reaction channel corresponding to the loss of an oxygen atom from the mass-selected metal oxide cluster, producing M x O y - 1 +, was only observed during the reactions of (V 2 O 5 ) n +, where n = 1, 2, or 3, with ethane and ethylene and during the reactions of ethylene with Nb 2 O 5 + . It is proposed that this reaction pathway is oxygen transfer from the mass-selected metal oxide cluster cation to the neutral hydrocarbon. This oxygen transfer channel is the major pathway observed during the course of reactions of V 2 O 5 +, V 4 O 10 +, and V 6 O 15 + with ethane and ethylene, but this reaction pathway is minor or nonexistent in the case of reactions of C 2 H 6 and C 2 H 4 with stoichiometrically equivalent niobium and tantalum oxide cluster cations. Additionally, the reactions of M x O y - with C 2 hydrocarbons were also examined. In contrast to the cation results, no reaction products were observed in studies of the interaction of group V transition metal oxide cluster anions with ethane and ethylene. The studies reveal that the identity of the metal, charge state, cluster stoichiometry, and geometric structure strongly influence the ability of the metal oxide cluster to transfer an oxygen atom to the neutral C 2 hydrocarbon.

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