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Theoretical investigation on photodechlorination mechanism of polychlorinated biphenyls

Author:
Wang, Se, Hao, Ce, Gao, Zhanxian, Chen, Jingwen, Qiu, Jieshan
Source:
Chemosphere 2014 v.95 pp. 200-205
ISSN:
0045-6535
Subject:
activation energy, benzene, dechlorination, deformation, dissociation, environmental fate, hydrogen, methanol, pollutants, polychlorinated biphenyls
Abstract:
Photodechlorination is a key process affecting the fate and effect of polychlorinated biphenyls (PCBs) in the environment. However, there are still numerous gaps in our knowledge, which become apparent in photodechlorination mechanism of PCBs. We investigated the conformations of 35 PCB congeners in the ground state and the first triplet excited state (T1), and predicted the photodechlorination pathway of the PCBs by calculating bond dissociation energies of the C−Cl bonds and activation energies of the C−Cl bond dissociation in the excited T1 state. Results show that the torsional degree of the two benzene rings of the PCBs depends on the number of ortho chlorines because of steric effect in the ground state. The two benzene rings of the PCBs with low photoreactivity tend to be coplanar and their torsional degree becomes lower in the excited T1 state compared with those in the ground state. The serious deformation and non-coplane of the benzene rings of some PCBs (e.g. PCB138) in the excited T1 state reduces the conjugation between the two benzene rings, implying that these PCBs have high photoreactivity. The dissociation of the C−Cl bond is the rate-determining step in the photodechlorination reactions of PCBs when the hydrogen donor is methanol. The main photodechlorination pathways predicted in this study are in good agreement with previous experimental results. Our results have provided new insights into mechanism of PCBs photodechlorination, which could be useful in the future in utilizing quantum chemistry calculation in investigating the environmental behavior and fate of organic pollutants.
Agid:
5452693