We report the controlled synthesis and structures of two isomeric gold nanoclusters, whose compositions are determined to be Au 23 (CCBu t ) 15 (denoted as Au 23 -1 and Au 23 -2) by single-crystal X-ray diffraction and matrixassisted laser desorption ionization time-of-flight mass spectrometry. This is the first time isomerism is discovered in alkynyl-protected gold nanoclusters. The metal-toligand ratios in these two clusters are different from known Au n (SR) m systems and have not been observed in the Au x (CCPh) y family. This pair of isomers exhibits different optical properties, although they have similar structures and identical components. For both Au 23 clusters, time-dependent density functional theory calculations revealed the frontier orbitals highest occupied molecular orbital (HOMO)−1, HOMO, and lowest unoccupied molecular orbital (LUMO) are mainly constructed from the Au 15 kernel and V-shaped alkynyl−gold motifs. The HOMO → LUMO transition of Au 23 -1 is optically forbidden, whereas it is allowed in Au 23 -2. It is also found that Au 23 -2 cluster can be transformed to Au 23 -1 spontaneously under ambient conditions. This work offers further insight into the synthesis and isomerism of all-alkynyl-protected gold nanoclusters and will stimulate more investigation of isomeric metal nanoclusters.

Two homoleptic alkynyl‐protected gold clusters with compositions of Na[Au25(C≡CAr)18] and (Ph4P)[Au25(C≡CAr)18] (Na⋅1 and Ph4P⋅1, Ar=3,5‐bis(trifluoromethyl)phenyl) were synthesized via a direct reduction method. 1 is a magic cluster analogous to [Au25(SR)18]− in terms of electron counts and metal‐to‐ligand ratio. Single‐crystal structure analysis reveals that 1 has an identical Au13 kernel to [Au25(SR)18]−, but adopts a distinctly different arrangement of the six peripheral dimer staple motifs. The steric hindrance of alkynyl ligands is responsible for the D3 arrangement of Au25. The introduction of alkynyl also significantly changes the optical absorption features of the nanocluster as supported by DFT calculations. This magic cluster confirms that there is a similar but quite different parallel alkynyl‐protected metal cluster universe in comparison to the thiolated one.

Atomically precise gold nanoclusters provide great opportunities to explore the relationship between the structure and properties of nanogold catalysts. A nanocluster consists of a metal core and a surface ligand shell, and both the core and shell have significant effects on the catalytic properties. Thanks to their precise structures, the active metal site of the clusters can be readily identified and the effects of ligands on catalysis can be disclosed. In this Minireview, we summarize recent advances in catalytic research of gold nanoclusters, emphasizing four strategies for constructing open metal sites, including by post‐treatment, the bulky ligands strategy, the surface geometric mismatch method, and heteroatom doping procedures. We also discuss the effects of ligands on the catalytic activity, selectivity, and stability of gold cluster catalysts. Finally, we present future challenges relating to gold cluster catalysis.

By directly reducing alkynyl–silver precursors, we successfully obtained a large alkynyl‐protected silver nanocluster, (C7H17ClN)3[Ag112Cl6(C≡CAr)51], which is hitherto the largest structurally characterized silver nanocluster in the alkynyl family. The cluster exhibits four concentric core–shell structures (Ag13@Ag42@Ag48@Ag9), and four types of alkynyl–silver binding modes are observed. Chloride was found to be critical for the stabilization and formation of the silver nanocluster. The release of chloride ions in situ from CH2Cl2 solvent has been confirmed by mass spectrometry. This study suggests that the combination of alkynyl and halide ligands will pave a new way for the synthesis of large silver nanoclusters.

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