Search

Atomically precise low‐nuclearity (n<10) silver nanoclusters (AgNCs) have garnered significant interest due to their size‐dependent optical properties and diverse applications. However, their synthesis has remained challenging, primarily due to their inherent instability. The present study introduces a new feasible approach for clustering silver ions utilizing highly negative and redox‐inert polyoxoniobates (PONbs) as all‐inorganic ligands. This strategy not only enables the creation of novel Ag‐PONb composite nanoclusters but also facilitates the synthesis of stable low‐nuclearity AgNCs. Using this method, we have successfully synthesized a small octanuclear rhombic [Ag8]6+ AgNC stabilized by six highly negative [LiNb27O75]14− polyoxoanions. This marks the first PONb‐protected superatomic AgNC, designated as {Ag8@(LiNb27O75)6} (Ag8@Nb162), with an aesthetically spherical core–shell structure. The crystalline Ag8@Nb162 is stable under ambient conditions, What's more, it is water‐soluble and able to maintain its molecular cluster structure intact in water. Further, the stable small [Ag8]6+ AgNC has interesting temperature‐ and pH‐dependent reversible fluorescence response, based on which a multiple optical encryption mode for anti‐counterfeit technology was demonstrated. This work offers a promising avenue for the synthesis of fascinating and stable PONb‐protected AgNCs and sheds light on the development of new‐type optical functional materials. [ABSTRACT FROM AUTHOR]

Only rarely have polyoxometalates been found to form core–shell nanoclusters. Here, we succeeded in isolating a series of rare giant and all‐inorganic core–shell cobalt polyoxoniobates (Co−PONbs) with diverse shapes, nuclearities and original topologies, including 50‐nuclearity {Co12Nb38O132}, 54‐nuclearity {Co20Nb34O128}, 62‐nuclearity {Co26Nb36O140} and 87‐nuclearity {Co33Nb54O188}. They are the largest Co−PONbs and also the polyoxometalates containing the greatest number of Co ions and the largest cobalt clusters known thus far. These molecular Co−PONbs have intriguing and atomically precise core–shell architectures comprising unique cobalt oxide cores and niobate oxide shells. In particular, the encapsulated cobalt oxide cores with different nuclearities have identical compositions, structures and mixed‐valence Co3+/Co2+ states as the different sized Co−O moieties of the bulk cubic‐spinel Co3O4, suggesting that they can serve as various molecular models of the cubic‐spinel Co3O4. The successful construction of the series of the Co−PONbs reveals a feasible and versatile synthetic method for making rare core–shell heterometallic PONbs. Further, these new‐type core–shell bimetal species are promising cluster molecular catalysts for visible‐light‐driven CO2 reduction. [ABSTRACT FROM AUTHOR]

Compounds with redox activities have appealing applications in catalytic, electronic and magnetic properties, but the redox inert of polyoxoniobates (PONbs) significantly limits their applications for a long time. In this work, we are able to integrate organophosphate and lanthanide cluster into PONb to create the first family of inorganic‐organic hybrid organophosphate‐Ln‐PONb composite clusters. These novel species not only present the first family of redox active PONbs that can be reduced to form long‐lived "heteropoly blues" under ambient conditions, but also a new photochromic system. More importantly, the analyses of the electronic configurations and photochromic properties for a series of designed proof‐of‐concept PONbs models allow us to discover a D‐f‐A electron transfer mechanism, that is, photoinduced electron is transferred from a photosensitive organophosphate electron donor (D) to the NbV electron acceptor (A) through the unoccupied 4 f‐orbitals of Ln (f). This work paves the way for developing diverse PONb‐based redox materials and expanding the possibility of the applications of PONbs in the redox chemistry. [ABSTRACT FROM AUTHOR]

Cup‐shaped molecules are of great interest due to their appealing architectures and properties. Compared with widely studied calixarenes, polyoxometalate‐based cup‐shaped molecules currently remain a virgin land waiting for exploration. In this work, we report the first discovery of two giant cup‐shaped inorganic–organic hybrid polyoxoniobates (PONbs) of {Cu12Nb120} and {Cd16Nb128}. The former integrates three tricyclic Nb24 clusters and a hexacyclic Nb48 cluster into a cup‐shaped molecule via a Cu12 metallacalixarene, while the latter unifies two tricyclic Nb24 clusters and a brand‐new pentacyclic Nb40 cluster into another cup‐shaped molecule via a hybrid Cd16 unit. With 132 and 144 metal centers, {Cu12Nb120} and {Cd16Nb128} show the largest two inorganic–organic hybrid PONbs known to date. [ABSTRACT FROM AUTHOR]