Circularly polarized luminescence was evidence in solid state for a chiral-at-metal Dy(iii) single-molecule magnet. This CPL is opposite for the enantiomers and develops when the relaxation of the magnetization for the Dy becomes slower.

Crystal structures and crystallization behaviors of a series of heterotrinuclear ZnII–LnIII–ZnII complexes, [(L)­ZnLnZn­(L)]­NO3 (Ln = La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Yb, Lu, and Y; H3L = 1,1,1-tris­[(3-methoxysalicylideneamino)­methyl]­ethane), were examined. Because the trinuclear complex cation has two asymmetric centers (Δ and Λ) at the ZnII sites resulting from the twist of the tripodal ligand arms, it was confirmed from the single-crystal X-ray diffraction (SC-XRD) analysis that these complexes have homochiral structures (i.e., Λ,Λ- or Δ,Δ-enantiomer) in the solid state. Among the series of compounds, various types of spontaneous resolution were observed, which were classified by the SC-XRD analysis (using the Flack parameter) or solid-state circular dichroism spectroscopy. The latter technique was used to determine the chirality of every single crystal and that of an entire bulk mixture of microcrystals obtained in a particular crystallization process. It was found that the TbIII complex, [(L)­ZnTbZn­(L)]­NO3·2MeOH (Zn–Tb–Zn), exclusively deposited the left-handed Λ-conglomerate in every crystallization experiment. This phenomenon may be termed “absolute spontaneous resolution.” It was also notable that only the lanthanoid­(III) ions with an even number of 4f electrons (Eu, Tb, Ho, and Lu) exhibited this unusual phenomenon. It was also attempted to deposit the opposite-handed Zn–Tb–Zn Δ-conglomerate, which could not be isolated from the ambient crystallization. Seeding of a crashed single-crystal Δ-conglomerate of [(L)­ZnYZn­(L)]­NO3·2MeOH (Zn–Y–Zn), which was isomorphic to Zn–Tb–Zn, into a saturated methanolic solution of Zn–Tb–Zn gave, for the first time, crystals of the corresponding Δ-conglomerate.