Abstract
Thiacalix[4]arenes as a family of promising ligands have been widely used to construct polynuclear metal clusters, but scarcely employed in silver nanoclusters. Herein, an anion-templated Ag(88) nanocluster (SD/Ag88a) built from p-tert-butylthiacalix[4]arene (H(4)TC4A) is reported. Single-crystal X-ray diffraction reveals that C(4)-symmetric SD/Ag88a resembles a metal-organic super calix comprised of eight TC4A(4-) as walls and 88 silver atoms as base, which can be deconstructed to eight [CrO(4)@Ag(11)(TC4A)(EtS)(4)(OAc)] secondary building units arranged in an annulus encircling a CrO(4)(2-) in the center. Local and global anion template effects from chromates are individually manifested in SD/Ag88a. The solution stability and hierarchical assembly mechanism of SD/Ag88a are studied by using electrospray mass spectrometry. The Ag(88) nanocluster represents the highest nuclearity metal cluster capped by TC4A(4-). This work not only exemplify the specific macrocyclic effects of TC4A(4-) in the construction of silver nanocluster but also realize the shape heredity of TC4A(4-) to overall silver super calix.