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.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
