Search

A 'passivated precursor' approach is developed for the efficient synthesis and isolation of all-alkynyl-protected gold nanoclusters. Direct reduction of dpa-passivated precursor Au-dpa (Hdpa=2,2'-dipyridylamine) in one-pot under ambient conditions gives a series of clusters including Au 22 (C≡CR) 18 (R=-C 6 H 4 -2-F), Au 36 (C≡CR) 24 , Au 44 (C≡CR) 28 , Au 130 (C≡CR) 50 , and Au 144 (C≡CR) 60 . These clusters can be well separated via column chromatography. The overall isolation yield of this series of clusters is 40 % (based on gold), which is much improved in comparison with previous approaches. It is notable that the molecular structure of the giant cluster Au 130 (C≡CR) 50 is revealed, which presents important information for understanding the structure of the mysterious Au 130 nanoclusters. Theoretical calculations indicated Au 130 (C≡CR) 50 has a smaller HOMO-LUMO gap than Au 130 (S-C 6 H 4 -4-CH 3 ) 50 . This facile and reliable synthetic approach will greatly accelerate further studies on all-alkynyl-protected gold nanoclusters., (© 2024 Wiley-VCH GmbH.)

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 H 2 O 2 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., (© 2024 Wiley-VCH GmbH.)

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 [Ag 21 (Ph 2 PO 2 ) 10 (p-CHOPhC≡C) 6 ]SbF 6 , 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., (© 2024 Wiley-VCH GmbH.)

The application of supramolecular templates in aligning atomically precise heterometal arrays is important for pursuing functional materials. Herein, we report that a bilayered supramolecular tri-deprotonated melamine dimer functions as an effective template in the construction of a heterometallic gold(I)-silver(I) macrocyclic cluster [μ 6 -(C 3 N 6 H 3 ) 3- ] 2 -Au I 6 Ag I 6 . X-ray single crystal structural analysis showed that a crown-like Au I 6 Ag I 6 macrocycle is aligned around two parallelly stacked μ 6 -(C 3 N 6 H 3 ) 3- moieties hold together with π-π interactions. Theoretical calculations revealed that the [μ 6 -(C 3 N 6 H 3 ) 3- ] 2 motif dominantly contributes to the near-occupied orbitals in the electronic structure, which is closely related to its luminescence properties. This work demonstrates that the supramolecular templates containing multiple symmetric binding sites may present a facile approach in the construction of functional metal clusters., (© 2023 Wiley-VCH GmbH.)

A facile strategy that directly reduces alkynyl-silver precursors and copper salts for the synthesis of bimetallic nanoclusters using the weak reducing agent Ph 2 SiH 2 is demonstrated. Two alkynyl-protected concentric-shell nanoclusters, (Ph 4 P) 2 [Ag 22 Cu 12 (C≡CR) 28 ] and (Ph 4 P) 3 [Ag 42 Cu 12 Cl(C≡CR) 36 ] (Ag 22 Cu 12 and Ag 42 Cu 12 Cl, R=bis(trifluoromethyl)phenyl), were successfully obtained and characterized by single-crystal X-ray diffraction and electro-spray ionization mass spectrometry. For the first time, a hybrid 55-atom two-shell Mackay icosahedron was found in Ag 42 Cu 12 Cl, which is icosahedral M 54 Cl instead of M 55 . The incorporation of a chloride in the metal icosahedron contributes to the stability of the cluster from both electronic and geometric aspects. Alkynyl ligands show various binding-modes including linear "RC≡C-Cu-C≡CR" staple motifs., (© 2023 Wiley-VCH GmbH.)

The reduction of alkynyl-silver and phosphine-silver precursors with a weak reducing reagent Ph 2 SiH 2 led to the formation of a novel silver nanocluster [Ag 93 (PPh 3 ) 6 (C≡CR) 50 ] 3+ (R=4-CH 3 OC 6 H 4 ), which is the largest structurally characterized cluster of clusters. This disc-shaped cluster has a Ag 69 kernel consisting of a bicapped hexagonal prismatic Ag 15 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., (© 2023 Wiley-VCH GmbH.)

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., (© 2022 Wiley-VCH GmbH.)

Anions have been used to regulate the structures and luminescence of heterometallic clusters. Introducing ClO 4 - into orange-emissive, butterfly-like [(C)(Au-PPhpy 2 ) 6 Ag 4 ](BF 4 ) 6 (1, PPhpy 2 =bis(2-pyridyl)phenylphosphine) leads to the formation of red-emissive [(C)(Au-PPhpy 2 ) 6 Ag 5 (ClO 4 ) 3 ](ClO 4 ) 4 (2) with a novel trigonal bipyramidal structure; employing PhCO 2 - gives yellow-emissive, hexagram-like [(C)(Au-PPhpy 2 ) 6 Ag 6 (PhCO 2 ) 3 ](BF 4 ) 5 (3). Notably, 1 exhibits weak luminescence in CH 2 Cl 2 /CH 3 OH=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., (© 2022 Wiley-VCH GmbH.)

Surface organic ligands are critical in dictating the structures and properties of atomically precise metal nanoclusters. In contrast to the conventionally used thiolate, phosphine and alkynyl ligands, nitrogen donor ligands have not been used in the protection for well-defined metal nanoclusters until recently. This review focuses on recent developments in atomically precise metal nanoclusters stabilized by different types of nitrogen donor ligands, in which the synthesis, total structure determination and various properties are covered. We hope that this review will provide insights into the rational design of N donor-protected metal nanoclusters in terms of structural and functional modulation., (© 2022 Wiley-VCH GmbH.)

We report the structures, stability and catalysis properties of two Ag 21 nanoclusters, namely [Ag 21 (H 2 BTCA) 3 (O 2 PPh 2 ) 6 ]SbF 6 (1) and [Ag 21 (C≡CC 6 H 3 -3,5-R 2 ) 6 (O 2 PPh 2 ) 10 ]SbF 6 (2) (H 4 BTCA=p-tert-butylthiacalix[4]arene, R=OMe). Both Ag 21 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 1S 2 1P 6 , while 2 has an incomplete shell configuration 1S 2 1P 2 . These two Ag 21 clusters show superior stability under ambient conditions, and 1 is robust even at 90 °C in toluene and under oxidative conditions (30 % H 2 O 2 ). 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., (© 2022 Wiley-VCH GmbH.)

A Au 55 nanocluster with the composition of [Au 55 (p-MBT) 24 (Ph 3 P) 6 ](SbF 6 ) 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 Au 55 nanocluster features a face-centered cubic (fcc) Au 55 kernel, different from the well-known two-shell cuboctahedral arrangement in Au 55 (Ph 3 P) 12 Cl 6 . The Au 55 cluster shows a wide optical absorption band with optical energy gap (E g =1.28 eV). It is found that the exclusion of chloride is crucial for the formation of the title cluster, otherwise rod-like [Au 25 (SR) 5 (PPh 3 ) 10 Cl 2 ] 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 Au 55 nanocluster exhibits high catalytic activity and selectivity for electrochemical reduction of CO 2 to CO; the Faradaic efficiency (FE) reaches 94.1 % at -0.6 V vs. reversible hydrogen electrode (RHE)., (© 2021 Wiley-VCH GmbH.)

Acetelyenediide (C 2 2- ) species have been encapsulated in bimetallic and trimetallic clusters: [(AuL) 6 Ag 7 (C≡C) 3 ](BF 4 ) 7 (2) and [(AuL) 6 AgCu 6 (C≡C) 3 ](BF 4 ) 7 (3), L=phenylbis(2-pyridyl)phosphine (PPhpy 2 ). 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)M 2 Ag (M=Ag/Cu) motifs sharing a common silver atom. TDDFT calculations showed Cu-doping significantly increases the energy level of (C 2 -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., (© 2021 Wiley-VCH GmbH.)

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 Au 13 precursors. This facile approach has proved to be very effective in the synthesis of the well-known magic cluster [Au 25 (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 Au 25 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., (© 2021 Wiley-VCH GmbH.)

The first all-amidinate-protected gold nanocluster [Au 28 (Ph-form) 12 ](OTf) 2 (Ph-form=N,N'-diphenylformamidinate) (Au 28 ) has been synthesized and structurally resolved. Single crystal X-ray diffraction reveals that Au 28 has a compact Au 4 @Au 24 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 CO 2 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 Au 28 /CNTs maintains stable potentials at ca. -0.69 V for 40 h with FE(CO)s>91 %. A superatomic electron configuration of 1S 2 1P 6 2S 2 1D 4 has been clarified by DFT computations, and the strong gold-ligand binding and geometric shell closure account for the superior stability of Au 28 ., (© 2021 Wiley-VCH GmbH.)

Silver nanoclusters containing Ag 0 atoms protected by amino acids were synthesized and characterized. Chiral superatomic silver nanoclusters [Ag 47 L 12 (C≡C t Bu) 16 ]BF 4 (L=l-/d-valine or l-/d-isoleucine) have been prepared by reducing AgC≡C t Bu and amino acids (AAs) with NaBH 4 . Single crystal X-ray diffraction revealed that these clusters have T symmetry, and the Ag 47 metal kernel can be viewed as a tetracapped truncated tetrahedron (Ag 17 ) surrounded with six W-shaped Ag 5 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 1S 2 1P 6 1D 10 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., (© 2021 Wiley-VCH GmbH.)

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[Au 25 L 18 ] (Au 25 ), [HNEt 3 ] 3 [Au 67 L 32 Cl 4 ] (Au 67 ), [HNEt 3 ] 4 [Au 106 L 40 Cl 12 ] (Au 106 ), L=3,5-bis(trifluoromethyl)-phenylacetylide. Au 67 and Au 106 are new clusters; the structures were determined by X-ray single-crystal diffraction. Au 67 contains a distorted Au 18 Marks decahedron shelled by an irregular Au 32 and further protected with two V-shaped Au 2 L 3 , 13 linear AuL 2 staples and 4 chlorides. Au 67 is the first structurally determined 34e superatomic gold nanocluster. Au 106 is composed of 106 Au atoms co-protected by alkynyls and chlorides. It has a Au 79 kernel, like in Au 102 (p-MBA) 44 . The surface structure of Au 106 includes 20 linear Au-alkynyl staples, 5 Cl-Au-Cl and 2 Cl-Au motifs. These three gold nanoclusters show size-dependent electrochemical properties., (© 2020 Wiley-VCH GmbH.)

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 Ph 3 P 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 [Au 23 (Ph 3 P) 10 (dpa) 2 Cl](SO 3 CF 3 ) 2 (Au 23 , dpa=dipyridylamido) has been successfully synthesized. Single crystal structural determination reveals that Au 23 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., (© 2020 Wiley-VCH GmbH.)

By directly reducing alkynyl-silver precursors, we successfully obtained a large alkynyl-protected silver nanocluster, (C 7 H 17 ClN) 3 [Ag 112 Cl 6 (C≡CAr) 51 ], which is hitherto the largest structurally characterized silver nanocluster in the alkynyl family. The cluster exhibits four concentric core-shell structures (Ag 13 @Ag 42 @Ag 48 @Ag 9 ), 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 CH 2 Cl 2 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., (© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

An alkynyl-protected gold nanocluster, Au 22 ( t BuC≡C) 18 (1), has been synthesized and its structure has been determined by single-crystal X-ray diffraction. The molecular structure consists of a Au 13 cuboctahedron kernel and three [Au 3 ( t BuC≡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., (© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

A golden fullerene Au 32 cluster has been synthesized with amido and phosphine ligands as the protecting agents. Single-crystal X-ray structural analysis revealed that this gold nanocluster, [Au 32 (Ph 3 P) 8 (dpa) 6 ] (SbF 6 ) 2 (Hdpa=2,2'-dipyridylamine), has a stable pseudo-I h Au 32 8+ core with S 6 symmetry, which features an Au 12 @Au 20 Keplerate cage co-protected by Ph 3 P 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., (© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Two homoleptic alkynyl-protected gold clusters with compositions of Na[Au 25 (C≡CAr) 18 ] and (Ph 4 P)[Au 25 (C≡CAr) 18 ] (Na⋅1 and Ph 4 P⋅1, Ar=3,5-bis(trifluoromethyl)phenyl) were synthesized via a direct reduction method. 1 is a magic cluster analogous to [Au 25 (SR) 18 ] - in terms of electron counts and metal-to-ligand ratio. Single-crystal structure analysis reveals that 1 has an identical Au 13 kernel to [Au 25 (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 D 3 arrangement of Au 25 . 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., (© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

The syntheses and properties of two bimetallic nanoclusters [Au 4 Ag 23 (C≡CtBu) 10 (dppf) 4 Cl 7 ](PF 6 ) 2 and [Au 5 Ag 24 (C≡CC 6 H 4 -p-tBu) 16 (dppf) 4 Cl 4 ](PF 6 ) 3 are reported. The Au atoms distributed in both the cores and the surface motifs are clearly determined. The two nanoclusters show distinctly different geometric structures and electronic properties, which are attributed to the subtle changes in the surface alkynyl structures., (© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Total structure determination of a ligand-protected gold nanocluster, Au 144 , has been successfully carried out. The composition of title nanocluster is Au 144 (C≡CAr) 60 (1; Ar=2-FC 6 H 4 -). The cluster 1 exhibits a quasi-spherical Russian doll-like architecture, comprising a Au 54 two-shelled Mackay icosahedron (Au 12 @Au 42 ), which is further enclosed by a Au 60 anti-Mackay icosahedral shell. The Au 114 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 Au 144 , 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 Au 144 , which had been long-pursued, but also provides an interesting example showing ligand effects on the optical properties of ligand protected metal nanoclusters., (© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

The controlled synthesis and structure determination of a bimetallic nanocluster Au 57 Ag 53 (C≡CPh) 40 Br 12 (Au 57 Ag 53 ) is presented. The metal core has a four-shell Au 2 M 3 @Au 34 @Ag 51 @Au 20 (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 Au 57 Ag 53 are arranged in an irregular manner with C 1 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., (© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

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 Au 44 (PhC≡C) 28 and Au 36 (PhC≡C) 24 . The Au 44 and Au 36 nanoclusters have fcc-type Au 36 and Au 28 kernels, respectively, as well as surrounding PhC≡C-Au-C 2 (Ph)Au-C≡CPh dimeric "staples" and simple PhC≡C bridges. The structures of Au 44 (PhC≡C) 28 and Au 36 (PhC≡C) 24 are similar to Au 44 (SR) 28 and Au 36 (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., (© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

An intensely luminescent gold(I)-silver(I) cluster [(C)(AuPPhpy 2 ) 6 Ag 6 (CF 3 CO 2 ) 3 ](BF 4 ) 5 (PPhpy 2 =bis(2-pyridyl)phenylphosphine) (3) is synthesized by the reaction of [(C)(AuPPhpy 2 ) 6 Ag 4 ](BF 4 ) 6 with AgCF 3 CO 2 . All eight faces of the octahedral C@Au 6 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 CF 3 CO 2 - ions is vital for the construction and emission properties of 3, as confirmed by DFT calculations. BF 4 - ions are involved in the protecting sphere of the metal core, as evidenced by 19 F NMR data. The participation of phosphines, CF 3 CO 2 - , and BF 4 - 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., (© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

A red-near-IR dual-emissive nanocluster with the composition [Au10 Ag2 (2-py-C≡C)3 (dppy)6 ](BF4 )5 (1; 2-py-C≡C is 2-pyridylethynyl, dppy=2-pyridyldiphenylphosphine) has been synthesized. Single-crystal X-ray structural analysis reveals that 1 has a trigonal bipyramidal Au10 Ag2 core that contains a planar Au4 (2-py-C≡C)3 unit sandwiched by two Au3 Ag(dppy)3 motifs. Cluster 1 shows intense red-NIR dual emission in solution. The visible emission originates from metal-to-ligand charge transfer (MLCT) from silver atoms to phosphine ligands in the Au3 Ag(dppy)3 motifs, and the intense NIR emission is associated with the participation of 2-pyridylethynyl in the frontier orbitals of the cluster, which is confirmed by a time-dependent density functional theory (TD-DFT) calculation., (© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

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 λ(max)=925 nm and the nature of the HOMO-LUMO transition is investigated by time-dependent DFT calculations., (© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

A 23-gold-atom nanocluster was prepared by NaBH4-mediated reduction of a solution of PhC≡CAu and Ph3PAuSbF6 in CH2Cl2. The cluster composition was determined to be [Au23(PhC≡C)9(Ph3P)6](2+) and single-crystal X-ray diffraction revealed that the cluster has an unprecedented Au17 kernel protected by three PhC2-Au-C2 (Ph)-Au-C2 Ph motifs and six Ph3P groups. The Au17 core can be viewed as the fusion of two Au10 units sharing a Au3 triangle. Electronic structure analysis from DFT calculations suggests that the stability of this unusual 12-electron cluster is a result of the splitting of the superatomic 1D orbitals under D3h symmetry of the Au17 kernel. The discovery and determination of the structure of the Au23 cluster demonstrates the versatility of the alkynyl ligand in leading to the formation of new cluster compounds., (© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

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., (© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

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., (© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Peanut clusters: Anion templates are used in a facile approach for the synthesis of high-nuclearity silver clusters. The cluster nuclearity can be controlled by adjusting the size of the templating anions and by using different alkynyl ligands. The largest silver alkynyl cluster, which consists of 35 silver(I) centers in the shape of a peanut, has been prepared by using chromate anions as templates (see picture).

Ten polymeric silver(I) double salts containing embedded acetylenediide: [(Ag2C2)2(AgCF3CO2)9(L1)3] (1), [(Ag2C2)2(AgCF3CO2)10(L2)3]H2O (2), [(Ag2C2)(AgCF3CO2)4(L3)(H2O)]0.75 H2O (3), [(Ag2C2)(1.5)(AgCF3CO2)7(L4)2] (4), [(Ag2C2)(AgCF3CO2)7(L5)2(H2O)] (5), [(Ag2C2) (AgC2F5CO2)7(L1)3(H2O)] (6), [(Ag2C2)(AgCF3CO2)7(L1)3(H2O)]2 H2O (7), [(Ag2C2)(AgC2F5CO2)6(L3)2] (8), [(Ag2C2)2(AgC2F5CO2)12(L4)2(H2O)4]H2O (9), and [(Ag2C2)(AgCF3CO2)6(L3)2(H2O)]H2O (10) have been isolated by varying the types of betaines, the perfluorocarboxylate ligands employed, and the reaction conditions. Single-crystal X-ray analysis has shown that 1-4 all have a columnar structure composed of fused silver(I) double cages, with C2(2-) species embedded in its stem and an exterior coat comprising anionic and zwitterionic carboxylates. For 5 and 6, single silver(I) cages are linked into a beaded chain through both types of carboxylate ligands. In 7, two different coordination modes of L1 connect the silver(I) polyhedra into a chain. For 8, the mu(2)-O,O' coordination mode of L3 connects the silver(I) double cages into a chain. Compound 9 exhibits a two-dimensional architecture generated from the cross-linkage of double cages by C2F5CO2-, L4, and [Ag2(C2F5CO2)2] units. Similar to 9, 10 is also a two-dimensional structure, which is formed by connecting the chains of linked double cages through [Ag2(CF3CO2)2] bridging.

Five silver(I) double salts containing embedded acetylenediide, [Ag([12]crown-4)(2)][Ag(10)(C(2))(CF(3)CO(2))(9)([12]crown-4)(2)(H(2)O)(3)] x H(2)O (2), [Ag(2)C(2) x 5 AgCF(3)CO(2) x (benzo[15]crown-5) x 2 H(2)O] x 0.5 H(2)O (3), [Ag(4)([18]crown-6)(4)(H(2)O)(3)][Ag(18)(C(2))(3)(CF(3)CO(2))(16)(H(2)O)(2.5)] x 2.5 H(2)O (4), [Ag(2)C(2) x 6 AgC(2)F(5)CO(2) x 2([15]crown-5)](2) (5), and [(Ag(2)C(2))(2) x (AgC(2)F(5)CO(2))(9) x ([18]crown-6)(2) x (H(2)O)(3.5)] x H(2)O (6), have been isolated by varying the types of crown ethers and anions employed. Single-crystal X-ray analysis has shown that complex 2 is composed of winding anionic chains with sandwiched [Ag([12]crown-4)(2)](+) ions accommodated in the concave cavities between them. In 3, silver(I) double cages each sandwiched by a couple of benzo[15]crown-5 ligands are linked by [Ag(2)(CF(3)CO(2))(2)] bridges to form a one-dimensional structure. For 4, an anionic silver column is generated through fusion of two kinds of silver polyhedra (triangulated dodecahedron and bicapped trigonal antiprism), and the charge balance is provided by aqua-ligated [Ag([18]crown-6)](+) ions. Complex 5 is a centrosymmetric hexadecanuclear supermolecule composed of two [(eta(5)-[15]crown-5)(2)(C(2)@Ag(7))(mu-C(2)F(5)CO(2))(5)] moieties connected through a [Ag(2)(C(2)F(5)CO(2))(2)] bridge. Compound 6 is a discrete supermolecule containing an asymmetric (C(2))(2)@Ag(13) cluster core capped by two [18]crown-6 ligands in mu(3)-eta(5) and mu(4)-eta(6) ligation modes.