Spin dynamics phenomena of a cerium(III) double-decker complex induced by intramolecular electron transfer.

Switchable spin dynamic properties in single-molecule magnets (SMMs) via an applied stimulus have applications in single-molecule devices. Many SMMs containing heavy lanthanoid ions with strong uniaxial magnetic anisotropy have been reported to exhibit SMM characteristics in the absence of an external magnetic field. On the other hand, SMMs containing light lanthanoid cerium(III) (Ce 3+ ) ions exhibit field-induced slow magnetic relaxation. We investigated the chemical conversion of a diamagnetic Ce 4+ ion (4f 0 ) to a paramagnetic Ce 3+ ion (4f 1 ) in Ce-phthalocyaninato double-decker complexes (TBA + [Ce(obPc) 2 ] - (1) and TBA + [Ce(Pc) 2 ] - (2)) which exhibit field-induced SMM behaviour due to a 4f 1 system. The phthalocyaninato ligands with electron-donating substituents (obPc 2- = 2,3,9,10,16,17,23,24-octabutoxyphthalocyaninato) in 1 have a significant effect on the valence state of the Ce ion, which is reflected in its magnetic properties due to the mixed valence state of the Ce ion. Given that Ce double-decker complexes with π-conjugated ligands undergo intramolecular electron transfer (IET) to the Ce ion mixed valence state, characterised by a mixture of 4f 0 and 4f 1 configurations, we examined the dynamic disorder inherent in IET influencing magnetic relaxation.