Small symmetry-breaking triggering large chiroptical responses of Ag(70) nanoclusters.

The origins of the chiroptical activities of inorganic nanostructures have perplexed scientists, and deracemization of high-nuclearity metal nanoclusters (NCs) remains challenging. Here, we report a single-crystal structure of Rac-Ag(70) that contains enantiomeric pairs of 70-nuclearity silver clusters with 20 free valence electrons (Ag(70)), and each of these clusters is a doubly truncated tetrahedron with pseudo-T symmetry. A deracemization method using a chiral metal precursor not only stabilizes Ag(70) in solution but also enables monitoring of the gradual enlargement of the electronic circular dichroism (CD) responses and anisotropy factor g(abs). The chiral crystals of R/S-Ag(70) in space group P2(1) containing a pseudo-T-symmetric enantiomeric NC show significant kernel-based and shell-based CD responses. The small symmetry breaking of T(d) symmetry arising from local distortion of Ag-S motifs and rotation of the apical Ag(3) trigons results in large chiroptical responses. This work opens an avenue to construct chiral medium/large-sized NCs and nanoparticles, which are promising for asymmetric catalysis, nonlinear optics, chiral sensing, and biomedicine.