Americium Oxalate: An Experimental and Computational Investigation of Metal–Ligand Bonding

• Published in: Inorganic chemistry 2023-03, Vol.62 (12), p.4814-4822
• Main Authors: Arteaga, Ana, Nicholas, Aaron D., Ducati, Lucas C., Autschbach, Jochen
• Format: Article
• Language: English
• Subjects: actinide; americium; coordination polymer; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; transplutonium
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/acs.inorgchem.2c03976

A novel actinide-containing coordination polymer, [Am­(C2O4)­(H2O)3Cl] (Am-1), has been synthesized and structurally characterized. The crystallographic analysis reveals that the structure is two-dimensional and comprised of pseudo-dimeric Am3+ nodes that are bridged by oxalate ligands to form sheets. Each metal center is nine-coordinate, forming a distorted capped square antiprism geometry with a C 1 symmetry, and features bound oxalate, aqua, and chloro ligands. The Am3+–ligand bonds were probed computationally using the quantum theory of atoms in molecules nd natural localized molecular orbital approaches to investigate the underlying mechanisms and hybrid atomic orbital contributions therein. The analyses indicate that the bonds within Am-1 are predominantly ionic and the 5f shell of the Am3+ metal centers does not add a significant covalent contribution to the bonds. Our bonding assessment is supported by measurements on the optical properties of Am-1 using diffuse reflectance and photoluminescence spectroscopies. The position of the principal absorption band at 507 nm (5L6′ ← 7F0′) is notable because it is consistent with previously reported americium oxalate complexes in solution, indicating similarities in the electronic structure and ionic bonding. Compound Am-1 is an active phosphor, featuring strong bright-blue oxalate-based luminescence with no evidence of metal-centered emission.