Naslov
Time-resolved study on the reactions of organic selenides with hydroxyl and oxide radicals, hydrated electrons, and H-atoms in aqueous solution, and DFT calculations of transients in comparison with sulfur analogues

Autori
Tobien, Thomas ; Bonifačić, Marija ; Naumov, Sergej ; Asmus, Klaus-Dieter

Izvornik
Physical Chemistry Chemical Physics (1463-9076) 12 (2010), 25; 6750-6758

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
radicals; selenides

Sažetak
A complementary experimental and quantum mechanical study has been undertaken on the reactivity, formation and properties of transients generated in the reaction of selected organic selenides with hydroxyl radicals, oxide radical ions, hydrated electrons and hydrogen atoms in aqueous solution. A detailed study of the •OH and O• reactions with Me2Se revealed the formation of the respective adduct-radicals as precursors of (Me2SeSeMe2)+ radical cations. In case of the neutral Me2Se•(OH) the conversion into the three-electron bonded species proceeds, in part, via the molecular (Me2SeOH2)+ radical cation. Absolute rate constants have been determined for all the underlying processes. The respective reactions with hydrated electrons and hydrogen atoms indicate that selenides exhibit a higher reactivity towards redox-active species than sulfides. A most interesting finding is that the reaction of Me2Se with H• atoms is faster (k = 4.1  109 M1 s1) than the reduction by hydrated electrons (k = 2.1  108 M1 s1), precluding an electron transfer as mechanistic background. The rationale is rather an effective dissociative attack of the hydrogen atom on the selenium. Both, the eaq and H• induced reductions of Me2Se and Me2S lead, under cleavage of •CH3 radicals, to the direct formation of selenol and thiol, respectively. Complementary quantum mechanical studies, performed with Density Functional Theory (DFT) Hybrid B3LYP and BHandHLYP methods, confirm this mechanism. They also reveal a generally higher thermodynamic stability of the Se-centered radicals relative to the S-centered ones, e.g., for the molecular radical anions (Me2Se)• (H 27 kJ mol1) and (Me2S)• (H 16 kJ mol1). Despite of these stabilization energies the calculations indicate an instantaneous Se/SCH3 bond lengthening in the respective molecular radical anions. The same applies for the reaction of Me2S and Me2Se with H• atoms. Here the calculations indicate, in fact, no thermodynamic stability of a tentative H-adduct which, therefore, is only a fictional transition state in the H•-induced •CH3-displacement process.

Izvorni jezik
Engleski

Znanstvena područja
Kemija

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