Spontaneous enantiomorphism in poly-phased alkaline salts of tris(oxalato)ferrate(III): Crystal structure of cubic NaRb5[Fe(C2O4)3]2

PIRO, O.E.; ECHEVERRÍA, G.A.; BARAN, E.J.

Acta Crystallographica Section E: Crystallographic Communications

International Union of Crystallography

Año: 2018 vol. 74 p. 905 - 909

We show here that the phenomenon of spontaneous resolution of enantiomers occurs during the crystallization of the sodium and rubidium double salts of the transition metal complex tris(oxalato)ferrate(III), namely sodium pentarubidium bis[tris(oxalato)ferrate(III)], NaRb5[Fe(C2O4)3]2. One enantiomer of the salt crystallizes in the cubic space group P4332 with Z = 4 and a Flack absolute structure parameter x = -0.01 (1) and its chiral counterpart in the space group P4132 with x = -0.00 (1). All metal ions are at crystallographic special positions: the iron(III) ion is on a threefold axis, coordinated by three oxalate dianions in a propeller-like conformation. One of the two independent rubidium ions is on a twofold axis in an eightfold coordination with neighbouring oxalate oxygen atoms, and the other one on a threefold axis in a sixfold RbO6 coordination. The sodium ion is at a site of D3 point group symmetry in a trigonal-antiprismatic NaO6 coordination.