LAUSR

Across the actinide period, the stability of the trivalent oxidation state predominates in the heavy actinides, making their chemical nature close to that of rare earth elements. The resemblance in their chemistry poses difficulties in separating heavy actinides from lanthanides, which is a vital separation in the minor actinide partitioning process. Actinide contraction has conventionally implied electrostatic actinide-ligand interactions among the heavy actinides. The present study challenges this conventional understanding and reveals increasing covalency in the actinide-ligand bond across Am to Cf. Complexes of Am, Cm, Bk, and Cf have been examined for their electronic structure with a focus on the nature of their interactions with different ligands within the framework of density functional theory, where the relativistic effects have been incorporated by using zero-order regular approximation and spin-orbit coupling. The choice of ligands selected for this study facilitates the effect of the donor atom as well as denticity to be accounted for. Hence, heavy actinide complexes of the N- and O-donor ligand dipicolinic acid, S and O mixed donor ligands of the Cyanex type, and an octadentate ligand N, N, N' N'-tetrakis[(6-carboxypyridin-2-yl)methyl]ethylenediamine have been optimized and evaluated. In each case energy decomposition analysis has been used to explicitly decompose the metal-ligand interaction energy into components which have then been analyzed. Irrespective of the hard-soft characteristics of donor atoms or the denticity of the ligands, steadily increased covalency has been observed across Am to Cf. Inspection of the ligand highest energy occupied molecular orbitals and metal orbitals sheds light on the origin of the unexpected covalency. An overall increase in bonding and also the orbital contribution along the Am-Cf series is clearly due to the enhancement in covalency, which is complementary to the orbital degeneracy induced covalency proposed very recently by Batista and co-workers.