Complexation of Astatine(III) with Ketones: Roles of NO<sub>3</sub><sup>–</sup>Counterion and Exploration of Possible Binding Modes
Jonathan D. Burns, E. E. Tereshatov, Bowen Zhang, G. Tăbăcaru, Lauren A. McIntosh, Steven J. Schultz, Laura A. McCann, Bryan M. Harvey, A. Hannaman, Kylie Lofton, Maxwell Sorensen, Amy L. Vonder Haar, Michael B. Hall, S. J. Yennello
Abstract
Ketones have been proven effective in extracting astatine(III) from aqueous solvents. Previous theoretical studies suggested a mechanism where the “sp2” lone pair on the carbonyl oxygen donates electron density into the π system of the AtO+ molecular cation to form a dative-type bond. In this study, co-extraction of NO3– as AtO(NO3)·(O═CR1R2) species into the organic phase appears to be a key factor. Adjusting the electronic properties of the ketone, by having an aryl group instead of an alkyl group in the alpha position of the ketone, increased the electron density on C═O, increased the bond strength between the ketone and AtO+, and in turn increased the extraction of 211At into the organic phase. Extraction with diketones shows dependence on the bridging distance between the two carbonyl moieties, where a C3 or longer bridge results in a 10-fold increase in extraction into the organic phase. DFT calculations show the longer bridge allows for the chelation of AtO(NO3) by either the second carbonyl or the phenyl ring.