Title Electron-induced reductive debromination of 2,3,4-tribromodiphenyl ether: a computational study
Authors Luo, Jin
Hu, Jiwei
Zhuang, Yuan
Wei, Xionghui
Huang, Xianfei
Affiliation Guizhou Normal Univ, Guizhou Prov Key Lab Informat Syst Mountainous Ar, Guiyang 550001, Peoples R China.
Stanford Univ, Dept Civil & Environm Engn, Stanford, CA 94305 USA.
Peking Univ, Dept Appl Chem, Coll Chem & Mol Engn, Beijing 100871, Peoples R China.
Keywords Anions
Debromination
DFT
2,3,4-Tribromodiphenyl Ether
POLYBROMINATED DIPHENYL ETHERS
BROMINATED FLAME RETARDANTS
NANOSCALE ZEROVALENT IRON
DENSITY-FUNCTIONAL THEORY
DIBENZO-P-DIOXINS
DECABROMODIPHENYL ETHER
DECHLORINATION
PBDES
AFFINITIES
REACTIVITY
Issue Date 2013
Publisher journal of molecular modeling
Citation JOURNAL OF MOLECULAR MODELING.2013,19,(8),3333-3338.
Abstract To better understand the mechanism of the electron induced elimination of the bromide anion, we examined at the B3LYP/6-31+G(d) level electron capture by 2,3,4-tribromodiphenyl ether (BDE-21) followed by the release of the bromide anion and a radical. Both the geometry and energy of the BDE-21 neutral and its possible anionic states were studied. A significant relationship was found between the total energy and the length of the C-Br bonds by the analysis of the potential energy surface for the anionic states. Debromination preference for the bromine substituted positions was theoretically evaluated as meta-Br > ortho-Br > para-Br. The reaction profiles of the electron-induced debromination of BDE-21 demonstrated that, in general, the presence of a solvent makes the electron induced reductive debromination of BDE-21 significantly more advantageous, and the stabilization effect of the solvent on the reaction intermediates would make the electron attachment and dissociation relatively effective in comparison with the results from the gas-phase calculations.
URI http://hdl.handle.net/20.500.11897/221462
ISSN 1610-2940
DOI 10.1007/s00894-013-1868-y
Indexed SCI(E)
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