Abstract
A series of europium(III) complexes with cyanoxime ligands were prepared. The IR spectroscopic data revealed that the ambidentate ligands were coordinated to the central europium(III) atom in either a tridentate or a bidentate manner. The Mössbauer isomer shift ( IS) values showed a correlation with the quadrupole splitting ( QS) values in all complexes. A plot of the IS values versus the QS values showed that with increasing electron density of the Eu(III) nucleus the symmetry of the electronic shell around the Eu(III) atom decreases.
Published Version
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