Please use this identifier to cite or link to this item: http://hdl.handle.net/1843/50318
Type: Artigo de Periódico
Title: HNO is produced by the reaction of NO with thiols
Authors: Sebastián Angel Suárez
Martina Muñoz
Lucia Alvarez
Mateus Fernandes Venâncio
Willian Ricardo Rocha
Damian Ezequiel Bikiel
Marcelo A. Marti
Fabio Doctorovich
Abstract: Azanone (nitroxyl, HNO) is a highly reactive compound whose biological role is still a matter of debate. One possible route for its formation is NO reduction by biological reductants. These reactions have been historically discarded due to the negative redox potential for the NO,H+/HNO couple. However, the NO to HNO conversion mediated by vitamins C, E, and aromatic alcohols has been recently shown to be feasible from a chemical standpoint. Based on these precedents, we decided to study the reaction of NO with thiols as potential sources of HNO. Using two complementary approaches, trapping by a Mn porphyrin and an HNO electrochemical sensor, we found that under anaerobic conditions aliphatic and aromatic thiols (as well as selenols) are able to convert NO to HNO, albeit at different rates. Further mechanistic analysis using ab initio methods shows that the reaction between NO and the thiol produces a free radical adduct RSNOH•, which reacts with a second NO molecule to produce HNO and a nitrosothiol. The nitrosothiol intermediate reacts further with RSH to produce a second molecule of HNO and RSSR, as previously reported.
Subject: Compostos aromáticos
Moléculas
Monômeros
Peptídeos
Proteínas
Tióis
Mecânica quântica
Método de Monte Carlo
language: eng
metadata.dc.publisher.country: Brasil
Publisher: Universidade Federal de Minas Gerais
Publisher Initials: UFMG
metadata.dc.publisher.department: ICX - DEPARTAMENTO DE QUÍMICA
Rights: Acesso Restrito
metadata.dc.identifier.doi: https://doi.org/10.1021/jacs.7b06968
URI: http://hdl.handle.net/1843/50318
Issue Date: 2017
metadata.dc.url.externa: https://pubs.acs.org/doi/10.1021/jacs.7b06968
Appears in Collections:Artigo de Periódico

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.