Holmium(iii) molecular nanomagnets for optical thermometry exploring the luminescence re-absorption effect.

Coordination complexes of lanthanide(3+) ions can combine Single-Molecule Magnetism (SMM) with thermally modulated luminescence applicable in optical thermometry. We report an innovative approach towards high performance SMM-based optical thermometers which explores tunable anisotropy and the luminescence re-absorption effect of HoIII complexes. Our concept is shown in dinuclear cyanido-bridged molecules, {[HoIII(4-pyridone)4(H2O)2][MIII(CN)6]}·nH2O (M = Co, 1; Rh, 2; Ir, 3) and their magnetically diluted analogues, {[HoIII x YIII 1-x (4-pyridone)4(H2O)2][MIII(CN)6]}·nH2O (M = Co, x = 0.11, 1@Y; Rh, x = 0.12, 2@Y; Ir, x = 0.10, 3@Y). They are built of pentagonal bipyramidal HoIII complexes revealing the zero-dc-field SMM effect. Experimental studies and the ab initio calculations indicate an Orbach magnetic relaxation with energy barriers varying from 89.8 to 86.7 and 78.7 cm-1 K for 1, 2, and 3, respectively. 1-3 also differ in the strength of quantum tunnelling of magnetization which is suppressed by hyperfine interactions, and, further, by the magnetic dilution. The YIII-based dilution governs the optical properties as 1-3 exhibit poor emission due to the dominant re-absorption from HoIII while 1@Y-3@Y show room-temperature blue emission of 4-pyridone. Within ligand emission bands, the sharp re-absorption lines of the HoIII electronic transitions were observed. Their strong thermal variation was used in achieving highly sensitive ratiometric optical thermometers whose good performance ranges, lying between 25 and 205 K, are adjustable by using hexacyanidometallates. This work shows that HoIII complexes are great prerequisites for advanced opto-magnetic systems linking slow magnetic relaxation with unique optical thermometry exploiting a luminescence re-absorption phenomenon.