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Article Dans Une Revue International Journal of Quantum Chemistry Symposium Année : 2010

Electronic effects and ring strain influences on the electron uptake by selenium-containing bonds

Résumé

The gas-phase electron attachment of thiaselena and diselena derivatives is investigated on model organic systems by ab initio calculations (level of theory MP2/DZP++). Electronic contributions favor the one-electron addition on selenium-containing compounds, with adiabatic electron affinities of 0.03, 0.24, and 0.43 eV, respectively, for dimethyldisulfide, dimethylselenenylsulfide, and dimethyldiselenide. This ensures the possibility of an excess electron binding on [BOND]Se[BOND]S[BOND] and [BOND]Se[BOND]Se[BOND] linkages. The so-formed radical anionic intermediates present a three-electrons two-centers 2c[BOND]3e bond, whose nature is confirmed by Mulliken spin densities and NBO analysis. They are stable towards dissociation, with a low barrier evaluated between about 25–60 kJ/mol. Cyclization strongly enhances dichalcogen propensity to fix an excess electron. Adiabatic electron affinities of a series of 1,2-thiaselena-cycloalkanes and 1,2-diselena-cycloalkanes are positive and range from 0.24 to 1.30 eV. This can be traced back to the release of ring strain energy upon one-electron addition: this geometrical effect is nevertheless less marked than for disulfide analogs. © 2009 Wiley Periodicals, Inc. Int J Quantum Chem, 2010

Dates et versions

hal-01116181 , version 1 (12-02-2015)

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Elise Dumont, Pierre-Francois Loos, Adele D. Laurent, Xavier Assfeld. Electronic effects and ring strain influences on the electron uptake by selenium-containing bonds. International Journal of Quantum Chemistry Symposium, 2010, 110 (3), pp.513-523. ⟨10.1002/qua.22072⟩. ⟨hal-01116181⟩
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