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Author:

Liu, Y.-D. (Liu, Y.-D..) (Scholars:刘永东) | Zhong, R.-G. (Zhong, R.-G..) (Scholars:钟儒刚)

Indexed by:

Scopus CSCD

Abstract:

The conversion of peroxynitrite (ONOO-) to nitrate (NO 3-) mediated by peroxynitrous acid (ONOOH) has been investigated at the CCSD/6-311G(d)//B3LYP/6-311+G(d,p) level. Two kinds of pathways for the title reaction were found. The results show that the energy barrier of isomerization through pathway 1 is around 25 kcal/mol in the gas phase. This value is significantly lower than that of isomerization without any catalysts. Thus, it indicates that ONOOH definitely makes the conversion from ONOO- to NO3- feasible. Although pathway 2 does not decrease the energy barrier of this isomerization, peroxynitric acid (O2NOOH) was obtained; moreover, this is a new pathway for this formation. In view of the results that peroxynitrate anion can decompose into nitrite and dioxygen, we conclude that our results are consistent with the experimental observation that nitrate, nitrite, and dioxygen are the main final products of the decay of peroxynitrite around pH 7.

Keyword:

DFT; Isomerization; Peroxynitrite; Peroxynitrous acid

Author Community:

  • [ 1 ] [Liu, Y.-D.]College of Life Science and Bioengineering, Beijing University of Technology, Beijing 100022, China
  • [ 2 ] [Zhong, R.-G.]College of Life Science and Bioengineering, Beijing University of Technology, Beijing 100022, China

Reprint Author's Address:

  • 刘永东

    [Liu, Y.-D.]College of Life Science and Bioengineering, Beijing University of Technology, Beijing 100022, China

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Source :

Jiegou Huaxue

ISSN: 0254-5861

Year: 2008

Issue: 2

Volume: 27

Page: 171-176

2 . 2 0 0

JCR@2022

ESI Discipline: CHEMISTRY;

JCR Journal Grade:3

Cited Count:

WoS CC Cited Count: 0

SCOPUS Cited Count:

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 6

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