O-atom transport catalysis by atomic cations in the gas phase:: Reduction of N2O by CO

被引:138
作者
Blagojevic, V
Orlova, G
Bohme, DK [1 ]
机构
[1] York Univ, Dept Chem, Ctr Res Mass Spectrometry, Toronto, ON M3J 1P3, Canada
[2] York Univ, Ctr Res Earth & Space Sci, Toronto, ON M3J 1P3, Canada
关键词
D O I
10.1021/ja044950m
中图分类号
O6 [化学];
学科分类号
0703 [化学];
摘要
Atomic cations (26), M+, have been shown to lie within a thermodynamic window for O-atom transport catalysis of the reduction of N2O by CO and have been checked for catalytic activity at room temperature with kinetic measurements using an inductively-coupled plasma/selected-ion flow tube (ICP/SIFT) tandem mass spectrometer. Only 10 of these 26 atomic cations were seen to be catalytic: Ca+, Fe+, Ge+, Sr+, Ba+, Os+, Ir+, Pt+, Eu+, and Yb+. The remaining 16 cations that lie in the thermodynamic window (Cr+, Mn+, Co+, Ni+, Cu+, Se+, Mo+, Ru+, Rh+, Sn+, Te+, Re+, Pb+, Bi+, Tm+, and Lu+) react too slowly at room temperature either in the formation of MO+ or in its reduction by CO. Many of these reactions are known to be spin forbidden and a few actually may lie outside the thermodynamic window. A new measure of efficiency is introduced for catalytic cycles that allows the discrimination between catalytic cations on the basis of the efficiencies of the two legs of the catalytic cycle. Also, a potential-energy landscape is computed for the reduction of N2O by CO catalyzed by Fe+(D-6) that vividly illustrates the operation of an ionic catalyst.
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收藏
页码:3545 / 3555
页数:11
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