Molecular Lanthanide Switches for Magnetism and Photoluminescence

Solvation of [(CNT)Ln(η${}^8$-COT)] (Ln=La, Ce, Nd, Tb, Er; CNT=cyclononatetraenyl, i.e., C${}_9$H${}_9$−; COT=cyclooctatetraendiid, i.e., C${}_8$H${}_8$${}^2-$) complexes with tetrahydrofuran (THF) gives rise to neutral [(η${}^4$-CNT)Ln(thf)${}_2$(η${}^8$-COT)] (Ln=La, Ce) and ionic [Ln(thf)${}_x$(η${}^8$-COT)][CNT] (x=4 (Ce, Nd, Tb), 3 (Er)) species in a solid-to-solid transformation. Due to the severe distortion of the ligand sphere upon solvation, these species act as switchable luminophores and single-molecule magnets. The desolvation of the coordinated solvents can be triggered by applying a dynamic vacuum, as well as a temperature gradient stimulus. Raman spectroscopic investigations revealed fast and fully reversible solvation and desolvation processes. Moreover, we also show that a Nd:YAG laser can induce the necessary temperature gradient for a self-sufficient switching process of the Ce(III) analogue in a spatially resolved manner.