Trapping an octahedral Ag<sub>6</sub> kernel in a seven-fold symmetric Ag<sub>56</sub> nanowheel.

Wang, Zhi; Su, Hai-Feng; Kurmoo, Mohamedally; Tung, Chen-Ho; Sun, Di; Zheng, Lan-Sun · Nat Commun · 2018

basic_science · Level V

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Abstract

High-nuclearity silver clusters are appealing synthetic targets for their remarkable structures, but most are isolated serendipitously. We report here six giant silver-thiolate clusters mediated by solvents, which not only dictate the formation of an octahedral Ag<sub>6</sub><sup>4+</sup> kernel, but also influence the in situ-generated Mo-based anion templates. The typical sevenfold symmetric silver nanowheels show a hierarchical cluster-in-cluster structure that comprises an outermost Ag<sub>56</sub> shell and an inner Ag<sub>6</sub><sup>4+</sup> kernel in the centre with seven MoO<sub>4</sub><sup>2-</sup> anion templates around it. Electrospray ionization mass spectrometry analyses reveal the underlying rule for the formation of such unique silver nanowheels. This work establishes a solvent-intervention approach to construct high-nuclearity silver clusters in which both the formation of octahedral Ag<sub>6</sub><sup>4+</sup> kernel and in situ generation of various Mo-based anion templates can be simultaneously controlled.