No abstract

Solid-state uranyl hybrid structures are often formed through unique intermolecular interactions occurring between a molecular uranyl anion and a charge-balancing cation. In this work, solid-state structures of the uranyl tetrachloride anion engaged in uranyl–cation and uranyl–hydrogen interactions were studied using density functional theory (DFT). As most first-principles methods used for systems of this type focus primarily on the molecular structure, we present an extensive benchmarking study to understand the methods needed to accurately model the geometric properties of these systems. From there, the electronic and vibrational structures of the compounds were investigated through projected density of states and phonon analysis and compared to the experiment. Lastly, we present a DFT + thermodynamics approach to calculate the formation enthalpies (ΔH f) of these systems to directly relate to experimental values. Through this methodology, we were able to accurately capture trends observed in experimental results and saw good quantitative agreement in predicted ΔH f compared to the value calculated through referencing each structure to its standard state. Overall, results from this work will be used for future combined experimental and computational studies on both uranyl and neptunyl hybrid structures to delineate how varying intermolecular interaction strengths relates to the overall values of ΔH f.

Hydrogen bonding networks within hexavalent uranium materials are complex and may influence the overall physical and chemical properties of the system. This is particularly true if hydrogen bonding takes places between the donor and the oxo group associated with the uranyl cation (UO 2 2+ ). In the current study, we evaluate the impact of charge-assisted hydrogen bonding on the vibrational modes of the uranyl cation using uranyl tricarbonate [UO 2 (CO 3 ) 3 ] 4– interactions with [Co(NH 3 ) 6 ] 3+ as the model system. Herein, we report the synthesis and structural characterization of five novel compounds, [Co(NH 3 ) 6 ]Cl(CO 3 ) ( Co_Cl_CO 3 ), [Co(NH 3 ) 6 ] 4 [UO 2 (CO 3 ) 3 ] 3 (H 2 O) 11.67 ( Co4U3 ), [Co(NH 3 ) 6 ] 3 [UO 2 (CO 3 ) 3 ] 2 Cl (H 2 O) 7.5 ( Co3U2_Cl ), [Co(NH 3 ) 6 ] 2 [UO 2 (CO 3 ) 3 ]Cl 2 ( Co2U_Cl ), and [Co(NH 3 ) 6 ] 2 [UO 2 (CO 3 ) 3 ]CO 3 ( Co2U_CO 3 ), which contain differences in the crystalline packing and extended hydrogen bonding networks. We show that these slight changes in the supramolecular assembly and hydrogen bonding networks result in the modification of modes as observed by infrared and Raman spectroscopy. We use density functional theory calculations to assign the vibrational modes and provide an understanding about how uranyl bond perturbation and changes in hydrogen bonding interactions can impact the resulting spectroscopic signals.