The electronic structure and various molecular properties of the actinide (An) dicarbides ThC2 and UC2 were investigated by relativistic quantum chemical calculations. We probe five possible geometrical arrangements: two triangular structures including an acetylide (C2) moiety, as well as the linear AnCC, CAnC and bent CAnC geometries. Our calculations at various levels of theory indicate that the triangular species are energetically more favorable, while the latter three arrangements proved to be higher-energy structures. Our SO-CASPT2 calculations give the ground-state molecular geometry for both ThC2 and UC2 as the symmetric (C2v) triangular structure. The similar and, also very close in energy, asymmetric (Cs) triangular geometry belongs to a different electronic state. DFT and single-determinant ab initio methods failed to distinguish between these two similar electronic states demonstrating the power of multiconfiguration ab initio methods to deal with such subtle and delicate problems. We report detailed data on the electronic structure and bonding properties of the most relevant structures.

POGANY Peter;  KOVACS Attila;  VARGA Z.;  BICKELHAUPT Matthias;  KONINGS Rudy; 

2012-02-07

AMER CHEMICAL SOC

JRC67136

1089-5639,   

http://pubs.acs.org/toc/jpcafh/116/1,    https://publications.jrc.ec.europa.eu/repository/handle/JRC67136,   

10.1021/jp210190m,