Multifunctional single-molecule magnets (SMMs) have sparked great interest, but chiral SMMs obtained via spontaneous resolution are rarely reported. We synthesized a series of chiral trinuclear hepta-coordinate lanthanide complexes [ZnII3LnIII3] (1 for Dy, 2 for Tb, 3 for Gd, and 4 for Dy0.07Y0.93) using the achiral flexible ligand H2L (2,2'-[1,2-ethanediylbis[(ethylimino)methylene]]bis[3,5-dimethylphenol]). The complexes crystallize in the chiral P63 group space, and two enantiomers of different chirality are spontaneously resolved. Three [Zn(L)Cl]- anions utilize the two phenoxy oxygen atoms of each L2- to coordinate with three lanthanide ions, respectively, and the three hepta-coordinate D5h lanthanide ions are arranged in a triangle. The chirality comes from the propeller arrangement of the peripheral three bidentate chelate L2- ligands like octahedral [M(AA)3]n+/- (M = transition metal ions; AA = bidentate chelate ligands, e.g., 2,2'-bipyridine, 1,10-phenathroline, ethylenediamine, acac- or oxalate). Complex 1 exhibits an AC susceptibility signal and is frequency-dependent, which is typical of SMMs. Complex 4, doped with a large amount of diamagnetic Y(III) in Dy(III), exhibits Ueff = 48.3 K and τ0 = 4.4 × 10-8 s in experiments. Complex 2 shows circularly polarized luminescence and apparent photoluminescence, typical of the f-f transitions of Tb(III).