Trapping an octahedral Ag<sub>6</sub> kernel in a seven-fold symmetric Ag<sub>56</sub> nanowheel.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 29844401.
- Also identified by DOI 10.1038/s41467-018-04499-9 and PMC identifier 5974400.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
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.