The crystal structure of the complex Li-3[Fe(C2O4)(3)]. 5H(2)O has bee
n determined by X-ray diffraction analysis. The coordination of the ir
on atom is a distorted octahedron composed of the oxygen atoms of thre
e oxalate ions. Two of the lithium ions are octrahedral and the third
one is tetrahedral. Infinite chains appear along the b-axis, with alte
rnation of Fe3+ and Li+ cations separated by oxalate anions. In agreem
ent with this, the Mossbauer spectrum consists of an asymmetric and st
rongly broadened absorption pattern, indicating the presence of both p
aramagnetic relaxation effects and quadrupolar interaction which resul
t from an Fe3+ interionic shortest distance of 6.559 Angstrom and from
a non-cubic iron environment, respectively.