Energies, Stability and Structure Properties of Radicals Derived from Organic Sulfides Containing an Acetyl Group after the •OH Attack: ab Initio and DFT Calculations vs Experiment-Reference-Cited by-同舟云学术

Energies, Stability and Structure Properties of Radicals Derived from Organic Sulfides Containing an Acetyl Group after the •OH Attack: ab Initio and DFT Calculations vs Experiment

Published:2008-07-01 Issue:30 Volume:112 Page:7015-7026
ISSN:1089-5639
Container-title:The Journal of Physical Chemistry A
language:en
Short-container-title:J. Phys. Chem. A

Author:

Bergès Jacqueline¹,Varmenot Nicolas¹,Scemama Anthony¹,Abedinzadeh Zohreh¹,Bobrowski Krzysztof¹

Affiliation:

1. LCT, UMR 7616, Université Pierre et Marie Curie, 4 Place Jussieu, 75230 Paris Cedex 5 France, Université René Descartes, 45, rue des Saints Pères, 75006 Paris, France, Laboratoire de Chimie Physique, UMR 8601 CNRS, Université Paris Descartes, 45, rue des Saints Pères, 75006 Paris, France, and Institute of Nuclear Chemistry and Technology, Dorodna 16, 03-195 Warsaw, Poland

Publisher

American Chemical Society (ACS)

Subject

Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jp711944v

Reference51 articles.

1. Sulfur-Centered Three-Electron Bonded Radical Species

2. Free radical oxidation of organic sulphur compounds in aqueous solution

3. Formation of positive ions and other primary species in the oxidation of sulphides by hydroxyl radicals

4. Formation of a sulphur-sulphur bridged radical cation during the oxidation of 1,4-dithian by hydroxyl radicals

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