A pair of enantiopure
Au13 nanoclusters have been enantioselectively synthesized
by chiral ligands with stereogenic centers at the phosphorus atoms.
Their structures are determined by X-ray crystallography, which are
typical models with a high symmetric core and chiral surface ligand
arrangement. Correlation between the crystallographic structure, the
calculation, and the circular dichroism (CD) study indicates that
helical ligand arrangement inducing the core into chiral distortion
accounts for the chiroptical activities in the visible region. A rare
example of cocrystallization of a mixture of diastereomers has been
observed for the first time for gold nanoclusters, reflecting the
lack of chiral self-sorting of the ligands.