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|Title: ||A density functional study of actinyl containing complexes|
|Authors: ||Berard, Joel J.|
|Supervisor: ||Schreckenbach, Georg (Chemistry)|
|Examining Committee: ||Budzelaar, Peter (Chemistry)Fayek, Mostafa Fayek (Geological Science)|
|Graduation Date: ||May 2008|
|Issue Date: ||7-May-2008|
|Citation: ||Berard, J.J., Shamov, G.A., and Schreckenbach, G., J. Phys. Chem. A, 2007. 111(42): p. 10789-10803.|
|Abstract: ||Density functional (DFT) methods are first used to study 22 of the most stable solution-phase UN4O12 isomers containing uranyl nitrate, UO2(NO3)2. Based on relative free energy calculations, 4 solution (a6, a5, a8, and a1) and 5 gas-phase isomers (a1, a2, a3, b1, and b2) are identified as the strongest candidates to exist and possibly predominate within their respective environments.
DFT is then applied to a new form of binucleating Schiff–base polypyrrolic macrocycles containing actinyl ions [AnO2]n+ (An = U, Np, Pu; n = 1, 2) and 3d transition metals (TM): Mn, Fe, Co, and Zn. Formal bond order evidence is provided for 24 TM to actinyl–endo–oxygen partial bond formations. Special structural cases are discussed. Redox potentials for AnVIO21/AnVO21– couples closely follow the Np > Pu > U trend seen for AnO2(H2O)52+/1+. Predictions of –1.10, 0.25, and 0.01 eV are made for U, Np, and Pu redox potentials.|
|Appears in Collection(s):||FGS - Electronic Theses & Dissertations (Public)|
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