摘要: Metal-complexed chiral macrocyclic architectures have attracted increasing research interests in circularly polarized luminescence owing to their distinctive structural and functional attributes. The method of metal coordination has emerged as a robust methodology for chirality induction in many systems. In this work, we engineered two rigid and flexible chiral organic ligands (L1 and L2) by synergizing the inherent planar chirality of pillar[5]arenes with tailored metal-coordination moieties. They demonstrate versatile coordination capabilities toward both 3d- and 4f-block metals, enabling modulation of luminescent characteristics with blue, green and red emissions. Four planar chiral complexes exhibiting CPL activity were synthesized through systematic coordination of L1/L2 with Zn2+, Eu3+, and Tb3+. The coordination processes effectively rigidify molecular conformations, leading to an enhanced CPL performance. Particularly, the Tb-L2 complex displays superior lanthanide-centered emission with a fluorescence quantum yield of ∼55% and an emission dissymmetry factor glum = 5.5 × 10−3. By engineering the substitution on pillar[5]arene scaffolds, we have established a metal-coordination platform with CPL characteristics, which paves the way in the design of new metal-based luminescent materials.