Hierarchical structural complexity in atomically precise nanocluster frameworks

The supramolecular chemistry of nanoclusters is a flourishing area of nano-research; however, the controllable assembly of cluster nano-building blocks in different arrays remains challenging. In this work, we report the hierarchical structural complexity of atomically precise nanoclusters in micrometric linear chains (1D array), grid networks (2D array) and superstructures (3D array). In the crystal lattice, the Ag(29)(SSR)(12)(PPh(3))(4) nanoclusters can be viewed as unassembled cluster dots (Ag(29)–0D). In the presence of Cs(+) cations, the Ag(29)(SSR)(12) nano-building blocks are selectively assembled into distinct arrays with different oxygen-carrying solvent molecules―Cs@Ag(29)(SSR)(12)(DMF)(x) as 1D linear chains (Ag(29)–1D), Cs@Ag(29)(SSR)(12)(NMP)(x) as 2D grid networks (Ag(29)–2D), and Cs@Ag(29)(SSR)(12)(TMS)(x) as 3D superstructures (Ag(29)–3D). Such self-assemblies of these Ag(29)(SSR)(12) units have not only been observed in their crystalline state, but also in their amorphous state. Due to the diverse surface structures and crystalline packing modes, these Ag(29)-based assemblies manifest distinguishable optical absorptions and emissions in both solutions and crystallized films. Furthermore, the surface areas of the nanocluster crystals are evaluated, the maximum value of which occurs when the cluster nano-building blocks are assembled into 2D arrays (i.e. Ag(29)–2D). Overall, this work presents an exciting example of the hierarchical assembly of atomically precise nanoclusters by simply controlling the adsorbed molecules on the cluster surface.