Oxidation of NO• by small oxygen species HO2- and O2•-: the role of negative charge, electronic spin and water solvation

被引:6
|
作者
Ryding, Mauritz Johan [1 ,2 ]
Fernandez, Israel [3 ]
Uggerud, Einar [1 ,2 ]
机构
[1] Univ Oslo, Mass Spectrometry Lab, POB 1033, NO-0315 Oslo, Norway
[2] Univ Oslo, Ctr Theoret & Computat Chem, Dept Chem, POB 1033, NO-0315 Oslo, Norway
[3] Univ Complutense Madrid, Fac Ciencias Quim, Dept Quim Organ 1, E-28040 Madrid, Spain
关键词
GAS-PHASE REACTIONS; PEROXYNITROUS ACID; NITRIC-OXIDE; HYDROGEN-PEROXIDE; STRUCTURAL REARRANGEMENTS; CORONA DISCHARGE; DIPOLE-MOMENT; IONS; CLUSTERS; CHEMISTRY;
D O I
10.1039/c6cp00290k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The reactions of HO2-(H2O)(n) and O-2(center dot-) (H2O)(n) clusters (n = 0-4) with NO center dot were studied experimentally using mass spectrometry; the experimental work was supported by quantum chemical computations for the case n = 0, 1. It was found that HO2- (H2O)(n) clusters were efficient in oxidizing NO center dot into NO2-, although the reaction rate decreases rapidly with hydration above n = 1. Superoxide-water clusters did not oxidize NO center dot into NO2- under the present experimental conditions (low pressure): instead a reaction occurred in which peroxynitrite, ONOO, was formed as a new cluster core ion. The latter reaction was found to need at least one water molecule present on the reactant cluster in order to enable the product to stabilize itself by evaporation of H2O.
引用
收藏
页码:9524 / 9536
页数:13
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