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A gold(I)‐cluster‐based twin‐cage has been constructed by post‐clustering covalent modification of a hexa‐aldehyde cluster precursor with triaminotriethylamines. The cages‐on‐cluster structure has double cavities and four binding sites, which show site‐discriminative binding for silver(I) and copper(I) guests. The guests in the tripodal hats affect the luminescence of the cluster: the tetra‐silver(I) host–guest complex is weakly red‐emissive, while the bis‐copper(I)‐bis‐silver(I) one is non‐emissive but is a stimuli‐responsive supramolecule. The copper(I) ion inside the tri‐imine cavity is oxidation sensitive, which enables the release of the bright emissive precursor cluster triggered by H2O2 solution. The hybridization of a cluster with cavities to construct a cluster‐based cage presents an innovative concept for functional cluster design, and the post‐clustering covalent modification opens up new avenues for finely tuning the properties of clusters. [ABSTRACT FROM AUTHOR]

The reduction of alkynyl‐silver and phosphine‐silver precursors with a weak reducing reagent Ph2SiH2 led to the formation of a novel silver nanocluster [Ag93(PPh3)6(C≡CR)50]3+ (R=4‐CH3OC6H4), which is the largest structurally characterized cluster of clusters. This disc‐shaped cluster has a Ag69 kernel consisting of a bicapped hexagonal prismatic Ag15 unit wrapped by six Ino decahedra through edge‐sharing. This is the first time that Ino decahedra are used as a building block to assemble a cluster of clusters. Moreover, the central silver atom has a coordination number of 14, which is the highest in metal nanoclusters. This work provides a diverse metal packing pattern in metal nanoclusters, which is helpful for understanding metal cluster assembling mechanisms. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

Anions have been used to regulate the structures and luminescence of heterometallic clusters. Introducing ClO4− into orange‐emissive, butterfly‐like [(C)(Au‐PPhpy2)6Ag4](BF4)6 (1, PPhpy2=bis(2‐pyridyl)phenylphosphine) leads to the formation of red‐emissive [(C)(Au‐PPhpy2)6Ag5(ClO4)3](ClO4)4 (2) with a novel trigonal bipyramidal structure; employing PhCO2− gives yellow‐emissive, hexagram‐like [(C)(Au‐PPhpy2)6Ag6(PhCO2)3](BF4)5 (3). Notably, 1 exhibits weak luminescence in CH2Cl2/CH3OH=1 : 1 (v : v) with a quantum yield (QY) of 0.05, whereas it was dramatically increased to 0.49 and 0.83 for 2 and 3, respectively. Theoretical calculation confirms that the involvement of anions in the electronic structures is responsible for the shifts of emission. The high QYs of 2 and 3 are attributed to the protection provided by ligands and anions. This work demonstrates that anions may serve as an extra designable factor beyond just counterions for functional metal clusters. [ABSTRACT FROM AUTHOR]

We report the structures, stability and catalysis properties of two Ag21 nanoclusters, namely [Ag21(H2BTCA)3(O2PPh2)6]SbF6 (1) and [Ag21(C≡CC6H3‐3,5‐R2)6(O2PPh2)10]SbF6 (2) (H4BTCA=p‐tert‐butylthiacalix[4]arene, R=OMe). Both Ag21 structures possess an identical icosahedral kernel that is surrounded by eight peripheral Ag atoms. Single‐crystal structural analysis and ESI‐MS revealed that 1 is an 8‐electron cluster and 2 has four free electrons. Theoretical results show that the P‐symmetry orbitals are found as HOMO‐1 and HOMO states in 1, and the frontier unoccupied molecular orbitals (LUMO, LUMO+1 and LUMO+2) show D‐character, indicating 1 is a superatomic cluster with an electronically closed shell 1S21P6, while 2 has an incomplete shell configuration 1S21P2. These two Ag21 clusters show superior stability under ambient conditions, and 1 is robust even at 90 °C in toluene and under oxidative conditions (30 % H2O2). Significantly, 2 exhibits much higher activity than 1 as catalyst in the reduction of 4‐nitrophenol. This work demonstrates that ligands can influence the electronic structures of silver clusters, and further affect their stability and catalytic performance. [ABSTRACT FROM AUTHOR]

A Au55 nanocluster with the composition of [Au55(p‐MBT)24(Ph3P)6](SbF6)3 (p‐MBT=4‐methylbenzenethiolate) is synthesized via direct reduction of gold‐phosphine and gold‐thiolate precursors. Single‐crystal X‐ray diffraction reveals that this Au55 nanocluster features a face‐centered cubic (fcc) Au55 kernel, different from the well‐known two‐shell cuboctahedral arrangement in Au55(Ph3P)12Cl6. The Au55 cluster shows a wide optical absorption band with optical energy gap (Eg=1.28 eV). It is found that the exclusion of chloride is crucial for the formation of the title cluster, otherwise rod‐like [Au25(SR)5(PPh3)10Cl2]2+ is obtained. The strategy to run synthetic reaction in the absence of halide leads to new members of phosphine/thiolate co‐protected metal nanoclusters. The Au55 nanocluster exhibits high catalytic activity and selectivity for electrochemical reduction of CO2 to CO; the Faradaic efficiency (FE) reaches 94.1 % at −0.6 V vs. reversible hydrogen electrode (RHE). [ABSTRACT FROM AUTHOR]

Acetelyenediide (C22−) species have been encapsulated in bimetallic and trimetallic clusters: [(AuL)6Ag7(C≡C)3](BF4)7 (2) and [(AuL)6AgCu6(C≡C)3](BF4)7 (3), L=phenylbis(2‐pyridyl)phosphine (PPhpy2). Single‐crystal X‐ray diffraction analysis revealed that they are isostructural and six silver atoms in 2 are replaced with copper in 3. Both clusters have a trefoil skeleton, which can be viewed as three trigonal bipyramidal (LAu‐C≡C‐AuL)M2Ag (M=Ag/Cu) motifs sharing a common silver atom. TDDFT calculations showed Cu‐doping significantly increases the energy level of (C2‐Cu)‐involved occupied orbital, thus inducing interesting transition coupling of dual‐emission at low temperature. This work not only provides a strategy for constructing heterometallic clusters, but also shows the prospect for pursuing novel thermochromic luminescent materials by incorporating multi‐congeneric metal components. [ABSTRACT FROM AUTHOR]

High‐yield and large‐scale synthesis are highly demanded for the studies of gold nanoclusters. We developed a "cluster from cluster" approach to assemble gold nanoclusters with preformed atomically precise Au13 precursors. This facile approach has proved to be very effective in the synthesis of the well‐known magic cluster [Au25(SR)18]−, which could prepare the target cluster in high yield (overall yield up to ≈100 %) at large scale (gram‐scale based on gold). This method can be applied in the synthesis of 10 Au25 clusters with different R groups. This work presents an important approach that may be extended to high‐yield and large‐scale synthesis of other metal nanoclusters. [ABSTRACT FROM AUTHOR]

The first all‐amidinate‐protected gold nanocluster [Au28(Ph−form)12](OTf)2 (Ph‐form=N,N′‐diphenylformamidinate) (Au28) has been synthesized and structurally resolved. Single crystal X‐ray diffraction reveals that Au28 has a compact Au4@Au24 tetrahedral core–shell structure of T symmetry, which is fully protected by 12 bridging formamidinate ligands. This cluster is quite robust as indicated by the fact that it can stay intact in solution at 80 °C for 6 d. It exhibits excellent catalytic performance for the electroreduction of CO2 with 96.5 % Faradaic efficiency (FE) at −0.57 V and a maximum TOF of 1731 h−1 at −0.87 V. Its superior stability is also manifested in the fact that the supported catalyst Au28/CNTs maintains stable potentials at ca. −0.69 V for 40 h with FE(CO)s>91 %. A superatomic electron configuration of 1S21P62S21D4 has been clarified by DFT computations, and the strong gold–ligand binding and geometric shell closure account for the superior stability of Au28. [ABSTRACT FROM AUTHOR]

Silver nanoclusters containing Ag0 atoms protected by amino acids were synthesized and characterized. Chiral superatomic silver nanoclusters [Ag47L12(C≡CtBu)16]BF4 (L=l‐/d‐valine or l‐/d‐isoleucine) have been prepared by reducing AgC≡CtBu and amino acids (AAs) with NaBH4. Single crystal X‐ray diffraction revealed that these clusters have T symmetry, and the Ag47 metal kernel can be viewed as a tetracapped truncated tetrahedron (Ag17) surrounded with six W‐shaped Ag5 units. The clusters are homochiral as evidenced by CD measurements. As for the strong CD signals, large contributions are found from the occupied Ag s,p states (superatomic D states) near the Fermi level. Electron counting revealed that these clusters are 18‐electron systems, suggesting they are superatomic clusters. The superatomic nature with a 1S21P61D10 configuration was supported by DFT calculations. This work paves the way of taking AAs as facile chiral induction agents for the synthesis of metal nanoclusters. [ABSTRACT FROM AUTHOR]

The synthesis and isolation of alkynyl/chloride‐protected gold nanoclusters is described. Silica gel column chromatography is effective in isolating gold nanoclusters from the as‐synthesized cluster mixture to give the clusters Na[Au25L18] (Au25), [HNEt3]3[Au67L32Cl4] (Au67), [HNEt3]4[Au106L40Cl12] (Au106), L=3,5‐bis(trifluoromethyl)‐phenylacetylide. Au67 and Au106 are new clusters; the structures were determined by X‐ray single‐crystal diffraction. Au67 contains a distorted Au18 Marks decahedron shelled by an irregular Au32 and further protected with two V‐shaped Au2L3, 13 linear AuL2 staples and 4 chlorides. Au67 is the first structurally determined 34e superatomic gold nanocluster. Au106 is composed of 106 Au atoms co‐protected by alkynyls and chlorides. It has a Au79 kernel, like in Au102(p‐MBA)44. The surface structure of Au106 includes 20 linear Au‐alkynyl staples, 5 Cl‐Au‐Cl and 2 Cl‐Au motifs. These three gold nanoclusters show size‐dependent electrochemical properties. [ABSTRACT FROM AUTHOR]

Gold nanoclusters with surface open sites are crucial for practical applications in catalysis. We have developed a surface geometric mismatch strategy by using mixed ligands of different type of hindrance. When bulky phosphine Ph3P and planar dipyridyl amine (Hdpa) are simultaneously used, steric repulsion between the ligands will reduce the ligand coverage of gold clusters. A well‐defined access granted gold nanocluster [Au23(Ph3P)10(dpa)2Cl](SO3CF3)2 (Au23, dpa=dipyridylamido) has been successfully synthesized. Single crystal structural determination reveals that Au23 has eight uncoordinated gold atoms in the shape of a distorted bicapped triangular prism. The accessibility of the exposed Au atoms has been confirmed quantitatively by luminescent titration with 2‐naphthalenethiol. This cluster has excellent performance toward selective oxidation of benzyl alcohol to benzaldehyde and demonstrates excellent stability due to the protection of negatively charged multidentate ligand dpa. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

An alkynyl‐protected gold nanocluster, Au22(tBuC≡C)18 (1), has been synthesized and its structure has been determined by single‐crystal X‐ray diffraction. The molecular structure consists of a Au13 cuboctahedron kernel and three [Au3(tBuC≡C)4] trimeric staples. The cluster 1 has strong luminescence in the solid state with a 15 % quantum yield, and it displays interesting thermochromic luminescence as revealed by temperature‐dependent emission spectra. The enhanced room‐temperature emission is characterized as thermally activated delayed fluorescence. [ABSTRACT FROM AUTHOR]

A golden fullerene Au32 cluster has been synthesized with amido and phosphine ligands as the protecting agents. Single‐crystal X‐ray structural analysis revealed that this gold nanocluster, [Au32(Ph3P)8(dpa)6] (SbF6)2 (Hdpa=2,2′‐dipyridylamine), has a stable pseudo‐Ih Au328+ core with S6 symmetry, which features an Au12@Au20 Keplerate cage co‐protected by Ph3P and dpa ligands. Quantum‐chemical studies were conducted to elucidate the origin of the special stability of this cluster, and suggest that it is electronically stabilized through metal–ligand interactions. Golden opportunity: A golden fullerene Au32 cluster has been synthesized through protection with amido and phosphine ligands. The stable pseudo‐Ih Au328+ core, which features an Au12@Au20 Keplerate cage, was confirmed to be electronically stabilized through metal–ligand interactions. [ABSTRACT FROM AUTHOR]

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. Magic clusters Na[Au25(C≡CAr)18] and (Ph4P)[Au25(C≡CAr)18] (Ar=3,5‐bis(trifluoromethyl)phenyl) exhibit novel connection between staples and the Au13 core. Steric hindrance caused by rigid ligand coordination preference accounts for the different geometric and electronic structures. [ABSTRACT FROM AUTHOR]

Abstract: Total structure determination of a ligand‐protected gold nanocluster, Au144, has been successfully carried out. The composition of title nanocluster is Au144(C≡CAr)60 (1; Ar=2‐FC6H4‐). The cluster 1 exhibits a quasi‐spherical Russian doll‐like architecture, comprising a Au54 two‐shelled Mackay icosahedron (Au12@Au42), which is further enclosed by a Au60 anti‐Mackay icosahedral shell. The Au114 kernel is enwrapped by thirty linear ArC≡C‐Au‐C≡CAr staple motifs. The absorption spectrum of 1 shows two bands at 560 and 620 nm. This spectrum is distinctly different from that of thiolated Au144, which was predicted to have an almost identical metal kernel and very similar ligands arrangement in 1. These facts indicate the molecule‐like behavior of 1 and significant involvement of ligands in the electronic structure of 1. The cluster 1 is hitherto the largest coinage metal nanocluster with atomically precise molecular structure in the alkynyl family. The work not only addresses the concern of structural information of Au144, which had been long‐pursued, but also provides an interesting example showing ligand effects on the optical properties of ligand protected metal nanoclusters. [ABSTRACT FROM AUTHOR]

Abstract: The controlled synthesis and structure determination of a bimetallic nanocluster Au57Ag53(C≡CPh)40Br12 (Au57Ag53) is presented. The metal core has a four‐shell Au2M3@Au34@Ag51 @Au20 (M=1/3 Au+2/3 Ag) architecture. In contrast to the previously reported large nanoclusters that have highly symmetric kernel structures, the metal atoms in Au57Ag53 are arranged in an irregular manner with C1 symmetry. This cluster exhibits excellent thermal stability and is robust under oxidative or basic conditions. The silver precursors play a key role in dictating the structures of the nanoclusters, which suggests the importance of the counteranions used. [ABSTRACT FROM AUTHOR]

For the first time total structure determination of homoleptic alkynyl-protected gold nanoclusters is reported. The nanoclusters are synthesized by direct reduction of PhC≡CAu, to give Au44(PhC≡C)28 and Au36(PhC≡C)24. The Au44 and Au36 nanoclusters have fcc-type Au36 and Au28 kernels, respectively, as well as surrounding PhC≡C-Au-C2(Ph)Au-C≡CPh dimeric 'staples' and simple PhC≡C bridges. The structures of Au44(PhC≡C)28 and Au36(PhC≡C)24 are similar to Au44(SR)28 and Au36(SR)24, but the UV/Vis spectra are different. The protecting ligands influence the electronic structures of nanoclusters significantly. The synthesis of these two alkynyl-protected gold nanoclusters indicates that a series of gold nanoclusters in the general formula Au x(RC≡C) y as counterparts to Au x(SR) y can be expected. [ABSTRACT FROM AUTHOR]

An intensely luminescent gold(I)-silver(I) cluster [(C)(AuPPhpy2)6Ag6(CF3CO2)3](BF4)5 (PPhpy2=bis(2-pyridyl)phenylphosphine) ( 3) is synthesized by the reaction of [(C)(AuPPhpy2)6Ag4](BF4)6 with AgCF3CO2. All eight faces of the octahedral C@Au6 core in 3 are capped, that is, six faces are capped by silver ions and two by tetrafluoroborates. Cluster 3 is intensely luminescent in solution with a quantum yield of 92 %. Ligation of CF3CO2− ions is vital for the construction and emission properties of 3, as confirmed by DFT calculations. BF4− ions are involved in the protecting sphere of the metal core, as evidenced by 19F NMR data. The participation of phosphines, CF3CO2−, and BF4− ions in the protection of the emissive core and the enhancement of the rigidity of the cluster result in the high emission efficiency. This is the first example of organic ligands and inorganic anions forming a rigid protecting sphere for luminescent coinage-metal clusters. [ABSTRACT FROM AUTHOR]

An alkynyl-protected gold nanocluster [Au24(CCPh)14(PPh3)4](SbF6)2 has been prepared by a direct reduction method. Single-crystal X-ray diffraction reveals that the molecular structure contains a Au22 core that is made of two Au13-centered cuboctahedra that share a square face. Two staple-like PhCCAuCCPh motifs are located around the center of the rod-like Au22 core. This Au24 nanocluster is highly emissive in the near-infrared region with λmax=925 nm and the nature of the HOMO-LUMO transition is investigated by time-dependent DFT calculations. [ABSTRACT FROM AUTHOR]

A cluster-based luminescent porous metal-organic framework has been constructed through a 'cluster linker' approach. The luminescent gold(I) cluster, prefunctionalized with pyrazinyl groups, was used as a cluster linker, similar to an organic linker, to connect silver ions in order to form a 3D framework. 1D channels with 1.1 nm diameter were observed in the framework. The cluster with its intrinsic luminescence was incorporated into a porous framework to give a luminescent bifunctional NbO net. This MOF shows solvatochromic behavior, and the interactions between solvent molecules and silver ions inside the channels account for the changes in absorption and emission spectra. [ABSTRACT FROM AUTHOR]

The chirality of a gold nanocluster can be generated from either an intrinsically chiral inorganic core or an achiral inorganic core in a chiral environment. The first structural determination of a gold nanocluster containing an intrinsic chiral inorganic core is reported. The chiral gold nanocluster [Au20(PP3)4]Cl4 (PP3=tris(2-(diphenylphosphino)ethyl)phosphine) has been prepared by the reduction of a gold(I)-tetraphosphine precursor in dichloromethane solution. Single-crystal structural determination reveals that the cluster molecular structure has C3 symmetry. It consists of a Au20 core consolidated by four peripheral tetraphosphines. The Au20 core can be viewed as the combination of an icosahedral Au13 and a helical Y-shaped Au7 motif. The identity of this Au20 cluster is confirmed by ESI-MS. The chelation of multidentate phosphines enhances the stability of this Au20 cluster. [ABSTRACT FROM AUTHOR]

Due to the stability issue, It is difficult to prepare a silver nanocluster bearing functional sites, especially at a large scale. We report the synthesis and structure of a stable silver nanocluster bearing multiple surface aldehyde groups [Ag21(Ph2PO2)10(p‐CHOPhC≡C)6]SbF6, which allows for postsynthesis modification such as surface functionalization through aldimine condensation to give homochiral clusters. Remarkably, the preparation of this cluster can be done in ~90 % high yield at gram scale, which facilitates further studies and potential applications. Through DFT calculations and geometric structure analysis, the high stability of this cluster is attributed to the geometric closure and electronic structure. This is the first time that an effective one‐pot method has been developed to synthesize functional silver nanoclusters in high yield. The title cluster will be useful in the development of a variety of cluster‐based materials. [ABSTRACT FROM AUTHOR]

Small anions play a big role in the preparation of an intensely luminescent gold(I)–silver(I) cluster. In their Communication on page 7117 ff. Q.‐M. Wang and co‐workers show that the stepwise addition of silver ions to the gold‐cluster precursor enhances the rigidity of the cluster. The emissive core is fully protected by organic ligands and inorganic anions, which results in high emission efficiency. [ABSTRACT FROM AUTHOR]

For the first time total structure determination of homoleptic alkynyl-protected gold nanoclusters is reported. The nanoclusters are synthesized by direct reduction of PhC≡CAu, to give Au44(PhC≡C)28 and Au36(PhC≡C)24. The Au44 and Au36 nanoclusters have fcc-type Au36 and Au28 kernels, respectively, as well as surrounding PhC≡C-Au-C2(Ph)Au-C≡CPh dimeric 'staples' and simple PhC≡C bridges. The structures of Au44(PhC≡C)28 and Au36(PhC≡C)24 are similar to Au44(SR)28 and Au36(SR)24, but the UV/Vis spectra are different. The protecting ligands influence the electronic structures of nanoclusters significantly. The synthesis of these two alkynyl-protected gold nanoclusters indicates that a series of gold nanoclusters in the general formula Au x(RC≡C) y as counterparts to Au x(SR) y can be expected. [ABSTRACT FROM AUTHOR]

High‐yield and large‐scale synthesis are highly demanded for the studies of gold nanoclusters. We developed a "cluster from cluster" approach to assemble gold nanoclusters with preformed atomically precise Au13 precursors. This facile approach has proved to be very effective in the synthesis of the well‐known magic cluster [Au25(SR)18]−, which could prepare the target cluster in high yield (overall yield up to ≈100 %) at large scale (gram‐scale based on gold). This method can be applied in the synthesis of 10 Au25 clusters with different R groups. This work presents an important approach that may be extended to high‐yield and large‐scale synthesis of other metal nanoclusters. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

Abstract: Total structure determination of a ligand‐protected gold nanocluster, Au144, has been successfully carried out. The composition of title nanocluster is Au144(C≡CAr)60 (1; Ar=2‐FC6H4‐). The cluster 1 exhibits a quasi‐spherical Russian doll‐like architecture, comprising a Au54 two‐shelled Mackay icosahedron (Au12@Au42), which is further enclosed by a Au60 anti‐Mackay icosahedral shell. The Au114 kernel is enwrapped by thirty linear ArC≡C‐Au‐C≡CAr staple motifs. The absorption spectrum of 1 shows two bands at 560 and 620 nm. This spectrum is distinctly different from that of thiolated Au144, which was predicted to have an almost identical metal kernel and very similar ligands arrangement in 1. These facts indicate the molecule‐like behavior of 1 and significant involvement of ligands in the electronic structure of 1. The cluster 1 is hitherto the largest coinage metal nanocluster with atomically precise molecular structure in the alkynyl family. The work not only addresses the concern of structural information of Au144, which had been long‐pursued, but also provides an interesting example showing ligand effects on the optical properties of ligand protected metal nanoclusters. [ABSTRACT FROM AUTHOR]