Abstract
The crystal structures of the rare-earth (RE) trirhodium diborides praseo-dymium trirhodium diboride, PrRh(3)B(2), neodymium trirhodium diboride, NdRh(3)B(2), and samarium trirhodium diboride, SmRh(3)B(2), were refined on the basis of single-crystal X-ray diffraction data. The crystal chemistry of RERh(3)B(2) (RE: Pr, Nd, and Sm) compounds has previously been analyzed mainly on the basis of powder samples [Ku et al. (1980 ▸). Solid State Commun. 35, 91-96], and no structural investigation by single-crystal X-ray diffraction has been reported so far. The crystal structures of the three hexa-gonal RERh(3)B(2) compounds are isotypic with that of CeRh(3)B(2); RE, Rh and B sites are situated on special positions with site symmetry 6/mmm (Wyckoff position 1a), mmm (3g) and m2 (2c), respectively. In comparison with the previous powder X-ray study of hexa-gonal RERh(3)B(2), the present redetermination against single-crystal X-ray data has allowed for the modeling of all atoms with anisotropic displacement parameters (ADPs). The ADPs of the Rh atom in each of the structures result in an elongated displacement ellipsoid in the direction of the stacking of the Rh kagomé-type layer. The features of obtained ADPs of atoms are discussed in relation to RERh(3)B(2)-type and analogous structures.