Abstract
From Mössbauer spectra of Fe (O2PF2)3 and Fe (O2PCl2) follows a distortion of the symmetric octahedral environment of Fe (III). Whereas in Fe (O2PCl2)3 only O-Atoms are ligands of Fe (III) in Fe (O2PF2) 3 both O- and F-Atoms have ligand-functions. Simple ionic forces between Fe (III) and the Dihalogenphosphatogroups are excluded as a result of Raman spectra.

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