Impact of lanthanide ion complexation and temperature on the chemical reactivity of ,,','-tetraoctyl diglycolamide (TODGA) with the dodecane radical cation.

The impact of trivalent lanthanide ion complexation and temperature on the chemical reactivity of ,,','-tetraoctyl diglycolamide (TODGA) with the -dodecane radical cation (RH˙) has been measured by electron pulse radiolysis and evaluated by quantum mechanical calculations. Additionally, Arrhenius parameters were determined for the reaction of the non-complexed TODGA ligand with the RH˙ from 10-40 °C, giving the activation energy ( = 17.43 ± 1.64 kJ mol) and pre-exponential factor ( = (2.36 ± 0.05) × 10 M s). The complexation of Nd(III), Gd(III), and Yb(III) ions by TODGA yielded [Ln(TODGA)(NO)] complexes that exhibited significantly increased reactivity (up to 9.3× faster) with the RH˙, relative to the non-complexed ligand: ([Ln(TODGA)(NO)] + RH˙) = (8.99 ± 0.93) × 10, (2.88 ± 0.40) × 10, and (1.53 ± 0.34) × 10 M s, for Nd(III), Gd(III), and Yb(III) ions, respectively. The rate coefficient enhancement measured for these complexes exhibited a dependence on atomic number, decreasing as the lanthanide series was traversed. Preliminary reaction free energy calculations-based on a model [Ln(TOGDA)] complex system-indicate that both electron/hole and proton transfer reactions are energetically unfavorable for complexed TODGA. Furthermore, complementary average local ionization energy calculations showed that the most reactive region of model ,,','-tetraethyl diglycolamide (TEDGA) complexes, [Ln(TEGDA)(NO)], toward electrophilic attack is for the coordinated nitrate (NO) counter anions. Therefore, it is possible that radical reactions with the complexed NO counter anions dominate the differences in rates seen for the [Ln(TODGA)(NO)] complexes, and are likely responsible for the reported radioprotection in the presence of TODGA complexes.