Engaging the terminal. Promoting halogen bonding interactions with uranyl oxo atoms

Engaging the nominally terminal oxo atoms of the linear uranyl (UO${}_2$${}^{2+}$) cation in non-covalent interactions represents both a significant challenge and opportunity within the field of actinide hybrid materials. An approach has been developed for promoting oxo atom participation in a range of non-covalent interactions, through judicious choice of electron donating equatorial ligands and appropriately polarizable halogen-donor atoms. As such, a family of uranyl hybrid materials was generated based on a combination of 2,5-dihalobenzoic acid and aromatic, chelating N-donor ligands. Delineation of criteria for oxo participation in halogen bonding interactions has been achieved by preparing materials containing 2,5-dichloro- (25diClBA) and 2,5-dibromobenzoic acid (25diBrBA) coupled with 2,2${}^{\prime }$-bipyridine (bipy) (1 and 2), 1,10-phenanthroline (phen) (3-5), 2,2${}^{\prime }$:6${}^{\prime }$,2${}^{\prime \prime }$-terpyridine (terpy) (6-8), or 4${}^{\prime }$-chloro-2,2${}^{\prime }$:6${}^{\prime }$,2${}^{\prime \prime }$-terpyridine (Cl-terpy) (9-10), which have been characterized through single crystal X-ray diffraction, Raman, Infrared (IR), and luminescence spectroscopy, as well as through density functional calculations of electrostatic potentials. Looking comprehensively, these results are compared with recently published analogues featuring 2,5-diiodobenzoic acid which indicate that although inclusion of a capping ligand in the uranyl first coordination sphere is important, it is the polarizability of the selected halogen atom that ultimately drives halogen bonding interactions with the uranyl oxo atoms. (© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim)