Cocrystallization of Two Negatively Charged Dimercaptomaleonitrile-Stabilized Silver Nanoclusters.

Studies on the assembly of atomically precise metal nanoclusters (NCs) are of great significance in the nanomaterial field, which has attracted increasing interest in the last few decades. Herein, we report the cocrystallization of two negatively charged atom-precise silver nanoclusters, the octahedral [Ag62(MNT)24(TPP)6]8- (Ag62) and the truncated-tetrahedral [Ag22(MNT)12(TPP)4]4- (Ag22) in a 1:2 ratio (MNT2- = dimercaptomaleonitrile, TPP = triphenylphosphine). As far as we know, a cocrystal containing two negatively charged NCs has seldom been reported. Single-crystal structure determinations reveal that the component Ag22 and Ag62 NCs both adopt core-shell structures. In addition, the component NCs were separately obtained by adjusting the synthetic conditions. This work enriches the structural diversity of silver NCs and extends the family of cluster-based cocrystals.

Stepwise Amplification of Circularly Polarized Luminescence in Chiral Metal Cluster Ensembles.

Chiral metal-organic frameworks (MOFs) are usually endowed by chiral linkers and/or guests. The strategy using chiral secondary building units in MOFs for solving the trade-off of circularly polarized luminescence (CPL)-active materials, high photoluminescence quantum yields (PLQYs) and high dissymmetry factors (|glum |) has not been demonstrated. This work directionally assembles predesigned chiral silver clusters with ACQ linkers through reticular chemistry. The nanoscale chirality of the cluster transmits through MOF's framework, where the linkers are arranged in a quasi-parallel manner and are efficiently isolated and rigidified. Consequently, this backbone of chiral cluster-based MOFs demonstrates superb CPL, high PLQYs of 50.3%, and |glum | of 1.2 × 10-2 . Crystallographic analyses and DFT calculations show the quasi-parallel arrangement manners of emitting linkers leading to a large angle between the electric and magnetic transition dipole moments, boosting CPL response. As compared, an ion-pair-direct assembly without interactions between linkers induces one-ninth |glum | and one-sixth PLQY values, further highlighting the merits of directional arrangement in reticular nets. In addition, a prototype CPL switching fabricated by a chiral framework is controlled through alternating ultraviolet and visible light. This work is expected to inspire the development of reticular chemistry for high-performance chiroptical materials.

Platonic and Archimedean solids in discrete metal-containing clusters.

Metal-containing clusters have attracted increasing attention over the past 2-3 decades. This intense interest can be attributed to the fact that these discrete metal aggregates, whose atomically precise structures are resolved by single-crystal X-ray diffraction (SCXRD), often possess intriguing geometrical features (high symmetry, aesthetically pleasing shapes and architectures) and fascinating physical properties, providing invaluable opportunities for the intersection of different disciplines including chemistry, physics, mathematical geometry and materials science. In this review, we attempt to reinterpret and connect these fascinating clusters from the perspective of Platonic and Archimedean solid characteristics, focusing on highly symmetrical and complex metal-containing (metal = Al, Ti, V, Mo, W, U, Mn, Fe, Co, Ni, Pd, Pt, Cu, Ag, Au, lanthanoids (Ln), and actinoids) high-nuclearity clusters, including metal-oxo/hydroxide/chalcogenide clusters and metal clusters (with metal-metal binding) protected by surface organic ligands, such as thiolate, phosphine, alkynyl, carbonyl and nitrogen/oxygen donor ligands. Furthermore, we present the symmetrical beauty of metal cluster structures and the geometrical similarity of different types of clusters and provide a large number of examples to show how to accurately describe the metal clusters from the perspective of highly symmetrical polyhedra. Finally, knowledge and further insights into the design and synthesis of unknown metal clusters are put forward by summarizing these "star" molecules.

Snapshots of key intermediates unveiling the growth from silver ions to Ag70 nanoclusters.

Nanoclusters (NCs) are considered as initial states of condensed matter, and unveiling their formation mechanism is of great importance for directional synthesis of nanomaterials. Here, we initiate the reaction of Ag(i) ions under weak reducing conditions. The prolonged reaction period provides a unique opportunity for revealing the five stages of the growth mechanism of 20-electron superatomic Ag70 NCs by a time-dependent mass technique, that is, aggregate (I) → reduction (II) → decomposition and recombination (III) → fusion (IV) → surface recombination and motif enrichment (V), which is different from the formation process applicable to the gold clusters. More importantly, the key intermediates, Ag14 without free electrons (0e) in the first (stage I) and Ag24 (4e) in the second (stage II), were crystallized and structurally resolved, and the later transformation rate towards Ag70 was further controlled by modulating solvents for easy identification of more intermediates. In a word, we establish a reasonable path of gradual expansion in size and electrons from Ag(i) ions to medium-sized 20e Ag70. This work provides new insights into the formation and evolution of silver NCs, and unveils the corresponding optical properties along with the process.

Achiral-Core-Metal Change in Isomorphic Enantiomeric Ag12Ag32 and Au12Ag32 Clusters Triggers Circularly Polarized Phosphorescence.

Understanding how the chiral or achiral section in chiral nanostructures contributes to circularly polarized light emission (CPLE) at the atomic level is of fundamental importance. Here, we report two pairs of atomically precise enantiomers of homosilver (R/S-Ag12Ag32) and heterometal (R/S-Au12Ag32) clusters. The geometrical chirality of R/S-Ag12Ag32 arises from the chiral ligand and interface consisting of positive moieties of Ag32(R/S-PS)24. The circular dichroism of R/S-Ag12Ag32 is active, but CPLE-silent. A complete metal change from Ag12 to Au12 in the achiral core section of S2-@M12@S8 engenders isomorphous heterometal R/S-Au12Ag32, which activates CPLE. We further quantify the contributions of achiral and chiral sections and for the first time unveil that heterometal bonding (Au12-Ag32) at the linkage varies the delocalization of orbitals and proportion of achiral and chiral section in electron transition-involved orbitals, thus activating CPLE. Based on these unique atomically precise homochiral metal clusters, our work provides a new insight into the contributions of achiral and chiral sections to the origin of chiroptical response of chiral metal clusters, paving the way to advance the development of CPLE nanoparticles.

Stepwise structure evolution from 2D cluster-based frameworks to silver(I) clusters.

A pair of 2D chiral frameworks, R-Ag5-1 and S-Ag5-1, with orange fluorescence were successfully synthesized. They were transformed to a thermodynamically favored denser stacking, R-Ag5-3 and S-Ag5-3, accompanied by a change in the luminescence and activating the CPL signal. The capture and structural determination of the intermediates (R-Ag5-2 and S-Ag5-2) reveal that the coordination instability of Na+ ions is the main cause of this transition.

Atomically Precise Enantiopure Bimetallic Janus Clusters.

Asymmetric bimetallic Janus nanocrystals with a side-by-side interface have unique properties and important applications. However, understanding their fundamental issues, including their formation mechanism, interfacial linkage, and related properties, remains challenging, as does the preparation of enantiopure samples. Atomically precise Janus bimetal nanoclusters would unequivocally resolve these issues, yet they have not been realized. Here, based on Au and transition metals (Cu/Cd), and employing an S/P biligand strategy, we prepare and structurally resolve four Janus nanoclusters, including racemate 6e Au 8 /Cu 4 , 6e R -/ S-Au 8 /Cu 4 enantiomers, and 2e racemate Au 3 /Cd. Their interfacial linkage is unambiguously resolved at the atomic level, superatomic orbital splitting emerges, and unique molecule-like electronic transitions and chiroptical properties are present; more importantly, the dipolar distribution of bicomponents leads to a maximum dipole moment of up to 45 D, which drives the formation of 1D nanowires through self-assembly. This work provides a fundamental knowledge of intermetallic nanomaterials and an avenue for the synthesis of Janus nanoclusters.

Phosphate anion-induced silver-chalcogenide cluster-based metal organic frameworks as dual-functional catalysts for detoxifying chemical warfare agent simulants.

Two porphyrinic silver-chalcogenide cluster-based MOFs were achieved using a phosphate anionic template strategy, and the highly photoactive organic building modules combined with Lewis acidic silver clusters allow both SCC-MOFs to be used as versatile catalysts for the simultaneous degradation of sulfur mustard and nerve agent simulants.

Composition-Dependent Enzyme Mimicking Activity and Radiosensitizing Effect of Bimetallic Clusters to Modulate Tumor Hypoxia for Enhanced Cancer Therapy.

Alloying is an efficient chemistry to tailor the properties of metal clusters. As a class of promising radiosensitizers, most previously reported metal clusters exhibit unitary function and cannot overcome radioresistance of hypoxic tumors. Here, atomically precise alloy clusters Pt2 M4 (M = Au, Ag, Cu) are synthesized with bright luminescence and adequate biocompatibility, and their composition-dependent enzyme mimicking activity and radiosensitizing effect is explored. Specifically, only the Pt2 Au4 cluster displays catalase-like activity, while the others do not have clusterzyme properties, and its radiosensitizing effect is the highest among all the alloy clusters tested. By taking advantage of the sustainable production of O2 via the decomposition of endogenous H2 O2 , the Pt2 Au4 cluster modulates tumor hypoxia as well as increases the efficacy of radiotherapy. This work thus advances the cluster alloying strategy to produce multifunctional therapeutic agents for improving hypoxic tumor therapy.

Small symmetry-breaking triggering large chiroptical responses of Ag70 nanoclusters.

The origins of the chiroptical activities of inorganic nanostructures have perplexed scientists, and deracemization of high-nuclearity metal nanoclusters (NCs) remains challenging. Here, we report a single-crystal structure of Rac-Ag70 that contains enantiomeric pairs of 70-nuclearity silver clusters with 20 free valence electrons (Ag70), and each of these clusters is a doubly truncated tetrahedron with pseudo-T symmetry. A deracemization method using a chiral metal precursor not only stabilizes Ag70 in solution but also enables monitoring of the gradual enlargement of the electronic circular dichroism (CD) responses and anisotropy factor gabs. The chiral crystals of R/S-Ag70 in space group P21 containing a pseudo-T-symmetric enantiomeric NC show significant kernel-based and shell-based CD responses. The small symmetry breaking of Td symmetry arising from local distortion of Ag-S motifs and rotation of the apical Ag3 trigons results in large chiroptical responses. This work opens an avenue to construct chiral medium/large-sized NCs and nanoparticles, which are promising for asymmetric catalysis, nonlinear optics, chiral sensing, and biomedicine.

Alkynyl-Stabilized Superatomic Silver Clusters Showing Circularly Polarized Luminescence.

We report a new enantiomeric pair of superatomic silver clusters, R/S-Ag17, prepared from chiral alkynyl ligands. R-Ag17 and S-Ag17 possess C3 symmetry and emit near-infrared (NIR) light with a quantum yield (QY) of 8.0% under ambient condition as well as NIR circularly polarized luminescence (CPL) as a result of the chirality of the excited states. Both experiments and theoretical calculations indicate for the first time that the CPL originates from transitions between superatomic 1Pz (along the C3 axis) and 1S orbitals. This work opens a new avenue for CPL-active metal nanoclusters by utilizing chiral alkynyl ligands and enlightens the chirality transfer from chiral protecting ligands to superatomic states in metal clusters.

Bacterial community in saline farmland soil on the Tibetan plateau: responding to salinization while resisting extreme environments.

BACKGROUND: Salinization damages the health of soil systems and reduces crop yields. Responses of microbial communities to salinized soils and their functional maintenance under high salt stress are valuable scientific problems. Meanwhile, the microbial community of the salinized soil in the plateau environment is less understood. Here, we applied metagenomics technology to reveal the structure and function of microorganisms in salinized soil of the Tibetan Plateau. RESULTS: The diversity of composition and function of microbial community in saline soil have changed significantly. The abundances of chemoautotrophic and acidophilic bacteria comprising Rhodanobacter, Acidobacterium, Candidatus Nitrosotalea, and Candidatus Koribacter were significantly higher in saline soil. The potential degradation of organic carbon in the saline soil, as well as the production of NO and N2O via denitrification, and the production of sulfate by sulfur oxidation were significantly higher than the non-saline soil. Both types of soils were rich in genes encoding resistance to environmental stresses (i.e., cold, ultraviolet light, and hypoxia in Tibetan Plateau). The resistance of the soil microbial communities to the saline environment is based on the absorption of K+ as the main mechanism, with cross-protection proteins and absorption buffer molecules as auxiliary mechanisms in our study area. Network analysis showed that functional group comprising chemoautotrophic and acidophilic bacteria had significant positive correlations with electrical conductivity and total sulfur, and significant negative correlations with the total organic carbon, pH, and available nitrogen. The soil moisture, pH, and electrical conductivity are likely to affect the bacterial carbon, nitrogen, and sulfur cycles. CONCLUSIONS: These results indicate that the specific environment of the Tibetan Plateau and salinization jointly shape the structure and function of the soil bacterial community, and that the bacterial communities respond to complex and harsh living conditions. In addition, environmental feedback probably exacerbates greenhouse gas emissions and accelerates the reduction in the soil pH. This study will provide insights into the microbial responses to soil salinization and the potential ecological risks in the special plateau environment.

An Unprecedented Bird Nest Molybdenum(V) Cobalto-Phosphate Nanosized Wheel Constructed from the [H55 (Mo24 O48 )(Co4 O)2 Co16 (PO4 )42 (py)6 (EtOH)2 (H2 O)11 ]3- Anion.

An unprecedented bird-nest high-nuclear molybdenum(V) cobalto-phosphate nanosized wheel modified by imidazole (im) and pyridine (py), {[H55 (Mo24 O48 )(Co4 O)2 Co16 (PO4 )42 (py)6 (EtOH)2 (H2 O)11 ]- @[(Him)2 (Hpy)]}(N-Et-py)(H2 PO4 )(py)7 (EtOH)⋅12 H2 O (1), has been successfully synthesized by self-assembly. The anionic huge wheel consists of two rare {Co4 O} squares, four {Co4 } tetramers, four {Mo4 } tetramers and four {Mo2 } dimers, linked by bridging oxygen atoms and [PO4 ] groups and encloses two imidazolium cations and a protonated pyridium for charge balance. Surprisingly, 1 represents the first twisted wheel-shaped cluster with a record high-nuclear molybdenum(V) cobalto-phosphate. The delocalized electron effects of the cluster are enhanced with the help of coordinated py ligands, which endows 1 with an excellent third-order nonlinear optical (NLO) response. Additionally, 1 also shows a better photocatalytic water oxidation activity than Co(NO3 )2 with the O2 production of 205 µmol during 6 h in the absence of the [Ru(bpy)3 ]2+ photosensitizer.

Multifunctional Polymolybdate-Based Metal-Organic Framework as an Efficient Catalyst for the CO2 Cycloaddition and as the Anode of a Lithium-Ion Battery.

A three-dimensional polymolybdate-based metal-organic framework (POMOF) consisting of Zn-ε-Keggin unit and organic linker, {[PMo8VMo4VIO37(OH)3Zn4][BPE]2}·[BPE] (1), was successfully obtained by the hydrothermal method. Compound 1 is composed of Zn-ε-Keggin units and BPE ligands, featuring a fascinating 5-fold interpenetrating framework with dia topology. The catalytic performance of compound 1 was investigated, and experiments showed that 1 could effectively facilitate the cycloaddition reaction of CO2 with epoxides as Lewis acid heterogeneous catalyst. Moreover, compound 1 also was studied as LIBs anode material, and it showed reversible capacity of 546 mA h g-1 at 100th cycle.

Cl--Templated Assembly of Novel Peanut-like Ln40Ni44 Heterometallic Clusters Exhibiting a Large Magnetocaloric Effect.

Two novel and fascinating high-nuclearity lanthanide-transition (4f-3d) heterometallic clusters were obtained based on an anion-template (Cl-) and ligand-controlled approach, formulated as [Gd40Ni44(CO3)12(CH3COO)4(IDA)44(C2O4)(µ2-O)4(µ3-OH)60(µ3-O)6(H2O)12]·Cl10·20H2O (abbreviated as Gd40Ni44, 1) and [Eu40Ni44(CO3)12(CH3COO)6(IDA)44(C2O4)(µ2-O)4(µ3-OH)62(µ3-O)4(H2O)12]·Cl10·23H2O (abbreviated as Eu40Ni44, 2), where H2IDA = iminodiacetic acid and H2C2O4 = oxalic acid. Structural analysis exhibits that the compounds 1 and 2 were both constructed by two enticing bowl-like anion units Ln20Ni22, featuring peanut-like structures. Besides, the assembly of Ln20Ni22 was templated by five Cl- ions. Magnetically, compound 1 shows a significant magnetocaloric effect, with -ΔSm = 36.05 J kg-1 K-1 at 3 K for ΔH = 7 T.

A huge novel polyoxometalate-based cluster Fe10P4W32 exhibiting prominent electrocatalytic activity for the oxygen evolution reaction and third-order NLO properties.

Two novel POM-based huge clusters modified by conjugated organic ligands (DAPSC), {Fe10P4W32} and {Fe8MoW18}, have been successfully isolated. Compound 1 consists of a novel huge inorganic building block {Fe10P4W32} and four organic groups DAPSC linked by ten iron ions and four sodium ions. The DAPSC ligands enhance the electric delocalization effects of polyoxoanions, leading to strengthening of the third-order nonlinear optical (NLO) responses of compounds 1-2. Additionally, the oxygen evolution reaction (OER) electrocatalytic activity and the magnetic properties of compound 1 have also been investigated.

Exploring the Magnetic Interaction of Asymmetric Structures Based on Chiral VIII8 Clusters.

Polyoxovanadates (III) are important class of polyoxometalates in molecular magnetism field, and particularly the systems which contain vanadium(III) centers. To date, only very few highly reduced vanadium polynuclear complexes were reported, which remains a significant challenge to synthesize novel polyoxovanadates, owing to the characteristics of easily oxidized vanadium(III). Herein, two unprecedented petaloid chiral octanuclear polyoxovanadates, l- and d-[H2N(CH3)2]12.5(H3N(CH2)2NH3)(H3O)1.5(VIIIµ2-OH)8(SO4)16·2H2O (L-, D-V8), have been successfully obtained by solvothermal method without any chiral auxiliary. Both L- and D-V8 compounds contain the motif eight-membered ring (Vµ2-O)8(SO4)16 constituted of three different chiral entangled loops with the V atoms as nodes. Bond valence calculation (BVC) analysis indicates that all the V ions existed in L, D-V8 are +3 value. The magnetic behavior of compounds indicated ferromagnetic coupling between vanadium(III) ions. To our knowledge, it is the first chiral highly reduced polyoxovanadates that exhibit excellent ferromagnetism.

Polyoxometalate-Based Well-Defined Rodlike Structural Multifunctional Materials: Synthesis, Structure, and Properties.

The unpredictability of the polyoxometalate (POM) coordination model and the diversity of organic ligands provide more possibilities for the exploration and fabrication of various novel POM-based materials. In this work, a series of POM-based lanthanide (Ln)-Schiff base nanoclusters, [Ln(H2O)2(DAPSC)]2[Ln(H2O)3(DAPSC)]2[(SiW12O40)]3·15H2O (Ln = Sm, 1; Eu, 2; Tb, 3), have been successfully isolated by the reaction of classical Keggin POMs, a Ln3+ ion, and a Schiff-base ligand [2,6-diacetylpyridine bis(semicarbazone), abbreviated as DAPSC]. Both the hindrance effect of the organic ligand and charge balance endow the cluster with fascinating structural features of discrete and linear arrangement. The title compounds with dimensions of ca. 4 × 1 × 1 nm3 are first trimeric polyoxometalate-based nanosized compounds, constructed by saturated POM anions (SiW12O404-, denoted as SiW12). Moreover, the properties (stability, electrochemistry, third-order nonlinear optics, and magnetism) of the compounds have also been studied.

Two new POM-based compounds modified by lanthanide-Schiff base complexes with interesting NLO properties.

Two POM-based lanthanide derivatives, namely {triaqua[2,6-diacetylpyridine bis(semicarbazone)-κ5O,N,N',N'',O']terbium(III)}-µ-oxido-[tricosa-µ2-oxido-dodecaoxido-µ12-phosphato-dodecamolybdenum(VI)] pentahydrate (1), [Tb(C11H15N7O2)(H2O)3][PMo12O40]·5H2O, and the dysprosium(III) analogue (2), have been isolated successfully by the reaction of Keggin-POM [PMo12O40]3- (abbreviated as PMo12), the Ln3+ ion and the Schiff base 2,6-diacetylpyridine bis(semicarbazone) (DAPSC) ligand under hydrothermal conditions. [Ln(DAPSC)(H2O)3][PMo12O40]·5H2O is a PMo12-supported cluster featuring a lanthanide-Schiff base complex [denoted Ln-L(Schiff base)]. Single-crystal X-ray diffraction analysis reveals that the LnIII ion is in a distorted tricapped trigonal prismatic arrangement, coordinated by six O atoms and three N atoms. Two O atoms and three N atoms are provided by one DAPSC ligand, while the additional O atoms originate from a PMo12 cluster and three water molecules. Hydrogen-bonding interactions between adjacent clusters form an interesting three-dimensional supramolecular structure. The identities of 1 and 2 were characterized by IR spectroscopy, thermogravimetric analysis and powder X-ray diffraction. Interestingly, both compounds possess excellent two-photon absorption (TPA) responses to the third-order nonlinear optics (NLO) (2264 GM for 1 and 941 GM for 2), suggesting that they have potential applications in the field of nonlinear optics (NLO). To our knowledge, 1 and 2 are the first POM-based Ln-L(Schiff base) complexes showing excellent two-photon responses. Meanwhile, the electrochemical properties of both compounds were studied in detail.

A rare three-dimensional POM-based inorganic metal polymer bonded by CO2 with high catalytic performance for CO2 cycloaddition.

An exceedingly rare three-dimensional CO2-coordinated inorganic polyoxoanion was prepared by a hydrothermal synthesis reaction. The CO2 ligand connects with two Zn-ε-Keggin cores in a linear and symmetrical µ2-η2o,o coordination pattern with a C[double bond, length as m-dash]O bond length of 1.099(112) Å. The new compound reported here exhibits not only appealing structures but also high catalytic activity for the cycloaddition of carbon dioxide with epoxides.