Abstract
A new general synthetic procedure for preparation of Na3[Fe(C2O4)3]·5H2O (1), Rb3[Fe(C2O4)3]·3H2O (2), and Cs3[Fe(C2O4)3]·2H2O (3) was developed. The crystal structures of these salts have been determined by single crystal X-ray diffraction. Salt 1 crystallizes in the monoclinic space group C2/c with Z = 8, salt 2 in P21/c with Z = 4, and salt 3 in P21/n with Z = 4. The three new salts and K3[Fe(C2O4)3]·3H2O, prepared for comparative purposes, were further characterized by infrared and 57Fe-Mössbauer spectroscopy. These spectra are discussed in comparison with those of related oxalato complexes.
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