RESUMEN
Here we report on the strong magneto-chiral dichroism (MChD) detected through visible and near-infrared light absorption up to 5.0 T on {Er5Ni6} metal clusters obtained by reaction of enantiopure chiral ligands and NiII and ErIII precursors. Single-crystal diffraction analysis reveals that these compounds are 3d-4f heterometallic clusters, showing helical chirality. MChD spectroscopy reveals a high gMChD dissymmetry factor of ca. 0.24 T-1 (T = 4.0 K, B = 1.0 T) for the 4I13/2 â 4I15/2 magnetic-dipole allowed electronic transition of the ErIII centers. This record value is 1 or 2 orders of magnitude higher than that of the d-d electronic transitions of the NiII ions and the others f-f electric-dipole induced transitions of the ErIII centers. These findings clearly show the key role that magnetic-dipole allowed transitions have in the rational design of chiral lanthanide systems showing strong MChD.
RESUMEN
The magnetic interaction between the total angular momentum (J) of the 4f electrons in a lanthanide ion and the orbital angular momentum (L) of a porphyrin in the photo-excited states of 5,10,15,20-tetraphenylporphyrinato Dy(III) complexes capped with a crown ether with one of two different symmetries, 12-crown-4 or 1-aza-12-crown-4, was investigated by temperature- and magnetic dependent magnetic circular dichroism (VT-VH MCD). The analysis was conducted on the complexes with different non-aromatic ligands to investigate how different symmetries of the non-aromatic ligands have an impact on the electronic interaction causing an anti-parallel orientation of J and L. The magnitude of the J-L interaction was determined from simulation-based fitting to experimental ratios. While in both cases an antiferromagnetic-type interaction between J and L was identified, an asymmetric non-aromatic ligand resulted in an increased magnitude of the J-L interaction.
RESUMEN
Interaction between the total angular momentum (J) of 4f electrons in lanthanides and the orbital angular momentum (L) of porphyrins in the photoexcited states was investigated by temperature-dependent and magnetic circular dichroism (MCD) for 5,10,15,20-tetraphenylporphyrinato (TPP) terbium(III) complexes with two different non-aromatic ligands i.e. 12-crown-4(1,4,7,10-tetraoxacyclododecane) and 1-aza-12-crown-4(1,4,7-trioxa-10-azacyclododecane). The two cases with different ligands were examined in order to understand how magnetic interaction depends on the symmetry of the non-aromatic ligands. The three absorption bands in the visible region, B(0,0), Q(1,0), and Q(0,0) bands, showed temperature-dependent MCD A term. For each band, the J-L interaction was determined from the simulation-based fitting to experimental ratios. An increase in the magnitude of the J-L interaction was observed when the second ligand was the aza-crown with a lower symmetry. Ab initio RASSCF/RASSI calculations were performed to explore the effect of the difference in the second ligand to the ligand centred excited states and the ligand-field-splitting structure on the metal-centred ground multiplet of J = 6.
