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The assembly of giant silver clusters by using macrocylic multidentate ligand remains a challenge. Here, the authors synthesize a chromate-templated 88-nuclei silver super calix and reveal the role of anion templating effects and a hierarchical assembly mechanism.

Vinyl azides generally act as 3-atom synthon through the fast release of molecular nitrogen, whereas keeping the azide group intact is more challenging. Here, the authors show a copper-catalyzed enantioselective cycloaddition of two types of vinyl azides generating a diverse pool of valuable chiral cyclic azides.

Gold nanoclusters are known to grow stepwise from gold-thiolate monomers and oligomers. Here, the authors find that the evolution of silver nanoclusters differs completely from that of gold: rather than following a bottom-up pathway, the clusters evolve from similarly-sized Ag-thiolate cluster intermediates.

Molecules exhibiting Möbius topology are fascinating but challenging synthetic targets. Here, the authors report the elegant synthesis and crystal structure of a catenane formed from two fully conjugated, interlocked Möbius nanohoops, and use theoretical calculations to understand its conformational stability and aromaticity.

Bioinspired Fe-Mo complexes are promising for the activation of small molecules, offering valuable insights into the interactions and transformations of unsaturated hydrocarbons with abundant metals. Here, the authors report the synthesis and mechanistic studies of FeMo carbyne complexes and unveil the pivotal role of H₂O as a proton shuttle.

Photoredox catalysis is an important approach for synthesizing fine chemicals from olefins, but the limited lifetime of radical cation intermediates severely restricts the efficiency. Here, the authors report that Ag3PO4 can efficiently catalyze intramolecular and intermolecular [2 + 2] and Diels–Alder cycloadditions under visible-light irradiation.

Naturally occurring hydrogenase enzymes are capable of efficient hydrogen production but low stability and high cost limits their industrial use. Here, the authors show that chitosan encapsulation improves the catalytic efficiency of a mimic of the diiron subsite of the H-cluster of [FeFe]-hydrogenase.

Exploration of molybdenum complexes as homogeneous hydrogenation catalysts has garnered significant attention, but hydrogenation of unactivated olefins under mild conditions are scarce. Here, the authors report the synthesis of a cationic Mo(II) complex, which exhibits intriguing reactivity toward C₂H₂ and H₂ under ambient pressure.

The synthesis of high-nuclearity copper(I) nanoclusters remains challenging due to their low stability. Now four high-nuclearity Cu(I) nanoclusters have been successfully isolated by introducing a bifunctional phosphoramide ligand into the Cu/RC≡CH assembly system, enhancing complex stability through cooperative bonding.

The assembly of cluster-based π-stacked porous supramolecular frameworks presents daunting challenges. Here, the authors report a dynamic and transformable supramolecular framework based on Cu12 cluster and C-H···π-stacking with permanent porosity

Metalloligands provide a potent strategy for manipulating the surface metal arrangements of metal nanoclusters (NCs), but their synthesis and subsequent installation onto metal NCs remains a significant challenge. Here, the authors demonstrate the synthesis of two atomically precise silver NCs by controlling reaction temperature and demonstrate thermal induced structure transformation between the clusters during a temperature-dependent assembly process.

Controlling the structural transformations of metal clusters is challenging. Here, the authors synthesize a silver nanocluster and study the structural changes that take place upon reaction with bipyridine derivatives.

The preparation of chiral monolayer-protected metal clusters is interesting for their potential applications in a variety of fields, including catalysis. Here, the authors synthesize chiral Ag₁₄ nanoclusters in an all-achiral environment, and decipher the origin of chirality at the molecular level; the solvent choice is key to achieve homochiral crystallization.

Understanding how one metal nanocluster transforms into another is of synthetic and fundamental importance. Here, the authors use mass spectrometry to reveal an acid-induced structural transformation between two Ag clusters that proceeds via a breakage-growth-reassembly mechanism.

High-nuclearity silver clusters are appealing synthetic targets for their remarkable structures, but most are isolated serendipitously. Here, the authors describe the rational use of solvents to form cluster-in-cluster silver nanowheels, which comprise an octahedral Ag₆⁴⁺ core surrounded by a Ag₅₆ cage of unusual seven-fold symmetry.

Controlling the partial reduction of quinolines is challenging, given the competing overreduction to tetrahydroquinolines. Here, the authors report a cobalt-amido cooperative catalyst for the selective, partial transfer hydrogenation of quinolines to 1,2-dihydroquinolines with H₃N·BH₃ as reductant.

Nested polyhedra are compelling but incredibly complex synthetic targets in cluster chemistry. Here, the authors synthesize a Ag₉₀ nanocluster comprising three concentric polyhedra with apparently incompatible octahedral (O_h) and icosahedral (I_h) symmetry, a mathematical oddity that is solved by the shells’ symmetric arrangement around rotational 2- and 3-fold axes.

A novel release mechanism of microcapsules is demonstrated, where the rate of core release can be solely controlled by magnetic field-induced deformation of microcapsules. Composite microcapsules are prepared with magnetic particles embedded in the polymer wall. It shows that the release rate is highly dependent on the strengths of the magnetic field and deformation frequency of the microcapsules.

Semiconducting quantum dots (QDs) can serve as light-absorbing components in efficient artificial photosynthetic systems for H₂ evolution. This Review describes how we can optimize QDs for H₂ evolution using sacrificial reductants, before moving on to sustainable strategies for the photolysis of biomass or H₂O.

A series of FeO-CeO₂ nanocomposite catalysts (FeCe-x) were successfully fabricated by hydrogen reduction of hydroxide precursors at temperatures (x) between 200–600 °C. A FeCe-300 catalyst with a Fe:Ce ratio of 2-1 exhibited excellent performance for photothermal CO₂ hydrogenation to CO (CO selectivity = 99.87%, CO production rate 19.61 mmol h⁻¹ g_cat⁻¹, excellent stability). The FeO phase was effective in promoting the reverse water-gas shift (RWGS, CO₂ + H₂ → CO + H₂O). Catalysts prepared at higher reduction temperatures contained both Fe⁰ and FeO, with the Fe⁰ catalyzing the Sabatier reaction (CO₂ + 4H₂ → CH₄ + 2H₂O) and thus lowering FeCe-x catalyst selectivity to CO.