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This work reports the interesting and unique cation‐exchange behaviors of the first indium‐bridged purely inorganic 3D framework based on high‐nuclearity polyoxoniobates as building units. Each nanoscale polyoxoniobate features a fascinating near‐icosahedral core–shell structure with six pairs of unique inorganic "molecular tweezers" that have changeable openings for binding different metal cations via ion‐exchanges and exhibit unusual selective metal‐uptake behaviors. Further, the material has high chemical stability so that can undergo single‐crystal‐to‐single‐crystal metal‐exchange processes to produce a dozen new crystals with high crystallinity. Based on these crystals and time‐dependent metal‐exchange experiments, we can visually reveal the detailed metal‐exchange interactions and mechanisms of the material at the atomic precision level. This work demonstrates a rare systematic and atomic‐level study on the ion‐exchange properties of nanoclusters, which is of significance for the exploration of cluster‐based ion‐exchange materials that are still to be developed. [ABSTRACT FROM AUTHOR]

Herein, a giant Sb‐rich polyoxometalate (POM) {Sb21Tb7W56} is reported, which contains the largest number of Sb atoms in a POM so far. The Sb‐rich POM has many interesting structural features and is a rare example of a soluble and water‐stable giant POM. Biomedical studies indicate that the Sb‐rich POM exhibits broad‐spectrum antitumor activity against various cancer cell lines by reactivating the P53‐dependent apoptotic processes and disrupting the mitochondrial membrane. In addition, this Sb‐rich POM was capable of suppressing the growth and metastasis of a breast cancer in vivo. This work demonstrates that Sb‐rich POMs are promising candidates for the development of new anticancer drugs. [ABSTRACT FROM AUTHOR]

The development of new‐type memristors with special performance is of great interest. Herein, an inorganic‐organic hybrid crystalline polyoxometalate (POM) with usual dynamic structures is reported and used as active material for fabricating memristor with unique temperature‐regulated resistive switching behaviors. The hybrid POM not only exhibits tunable thermochromic properties, but also thermal‐induced reversible aggregation and disaggregation reactions, leading to reversible structural transformations in SCSC fashion. Further, the memory device using the hybrid POM as active layer exhibits uncommon performance, which can keep resistive switching silent in the low temperature range of 30–150 °C, but show nonvolatile memory behavior in the high temperature range of 150–270 °C. Particularly, the silent and working states at three special temperatures (30, 150 and 270 °C) can be monitored by chromism. The correlation between structure and resistive switching property of the material has been discussed. The work demonstrates that crystalline inorganic‐organic hybrid POMs are promising materials for making memristors with superior performance. [ABSTRACT FROM AUTHOR]

In this paper, we report a series of novel mixed‐metal‐substituted organic‐inorganic hybrid polyoxometalates (POMs) H3[(CH3)4N]14[NaLn(PW11O39)3]·18H2O (1‐Ln, Ln = Nd, Sm, Eu) via one‐pot solvothermal synthesis methods, which present the first series of polyoxometalate trimers composed of both alkali‐metal‐ and lanthanide‐substituted keggin‐type POMs. The trimeric heterometallic polyoxoanions in 1‐Ln show an interesting linear arrangement and can be further packed together to generate a packing structure with cations [(CH3)4N]+ and H3O+ filling the gaps between polyoxoanions. Compounds 1‐Ln are characterized by single‐crystal X‐ray diffraction analysis, TGA, IR and PXRD. Additionally, the luminescence and proton conductive properties of 1‐Ln are also characterized. A series of unprecedented linear mixed‐metal‐substituted organic‐inorganic hybrid polyoxometalate trimers H3[(CH3)4N]14[NaLn(PW11O39)3]·18H2O (1‐Ln, Ln = Nd, Sm, Eu), composed of both alkali‐metal‐ and lanthanide‐substituted keggin‐type POMs, show interesting luminescence and proton conductive properties. [ABSTRACT FROM AUTHOR]

This work demonstrates that the use of high‐negative and high‐symmetry lacunary polyoxometalates (POMs) for the clustering of alkali metal ions is a feasible strategy not only for the formation of rare high‐nuclearity alkali‐metal clusters but also for the construction of new‐type all‐inorganic ionic porous materials. By the strategy, an unprecedented high‐nuclearity K‐H2O cluster {K42(H2O)60} with core–shell K6@K36 configuration is stabilized by 8 C3v‐symmetry trivacant POMs [GeW9O34]10−, forming a novel giant ionic alkali‐metal‐POM composite cluster {K42Ge8W72O272(H2O)60} with more than 100 metal centers. The incorporated 42‐nuclearity K‐H2O cluster {K42(H2O)60} exhibits the highest‐nuclearity alkali‐metal‐water cluster known to date in POM chemistry. Further, the giant {K42Ge8W72O272(H2O)60} clusters can be linked by another kind of alkali metal ions Na+ to generate a fascinating three‐dimensional all‐inorganic ionic porous framework with high chemical stability, proton conductivity, and water vapor adsorption. Giant ionic cluster: The utilization of highly negative polyoxometalates for the clustering of alkali metal cations has allowed the synthesis of a rare all‐inorganic ionic porous material built from novel giant ionic clusters {K42Ge8W72O272(H2O)60} (K42W72), which exhibits high proton conductivity. The K42W72 not only is among the largest ionic clusters but also contains unprecedented core–shell K6@K36‐H2O cage. [ABSTRACT FROM AUTHOR]

Abstract: A protein‐sized (ca. 4.2×4.2×3.6 nm3) non‐biologically derived molecule {Nb288O768(OH)48(CO3)12} (Nb288) containing up to 288 niobium atoms has been obtained, which is by far the largest and the highest nuclearity polyoxoniobate (PONb). Particularly, in terms of metal nuclearity number, Nb288 is the second largest cluster so far reported in classic polyoxometalate chemistry (V, Mo, W, Nb, and Ta). Nb288 can be described as a giant windmill‐like cluster aggregate of six nanoscale high‐nuclearity PONb units {Nb47O128(OH)6(CO3)2} (Nb47) joined together by six additional Nb ions. Interestingly, the 47‐nuclearity Nb47 units generated in situ can be isolated and bridged by copper complexes to form an inorganic–organic hybrid three‐dimensional PONb framework, which exhibits effective catalytic activity for hydrolyzing nerve agent simulant of dimethyl methylphosphonate. The unique Nb47 cluster also provides a new type of topology to very limited family of Nb‐O clusters. [ABSTRACT FROM AUTHOR]

A series containing the highest nuclearity polyoxoniobate (PONb) nanoclusters, ranging from dimers to tetramers, has been obtained. They include one 114-nuclear {Li8⊂Nb114O316}, one 81-nuclear {Li3K⊂Nb81O225}, and one 52-nuclear {H4Nb52O150}. The Nb nuclearity of these PONbs is remarkably larger than those of all known high-nuclearity PONbs (≤32). Furthermore, the introduction of 3d Cu2+ ions can lead to the generation of extended inorganic-organic hybrid frameworks built from novel, high-nuclearity, nanoscale heterometallic PONb building blocks {H3Cu3Nb78O222} or {H3Cu4(en)Nb78O222}. These building blocks also contain the largest number of Nb centers of any heterometallic PONbs reported to date. The synthesis of new-type PONbs has long been a challenging subject in PONb chemistry. [ABSTRACT FROM AUTHOR]

A series of polyoxometalates (POMs) that incorporate the highest-nuclearity Ln clusters that have been observed in such structures to date (Ln26 , Ln=La and Ce) are described, which exhibit giant multishell configurations (Ln⊂W6⊂Ln26⊂W100). Their structures are remarkably different from known giant POMs that feature multiple Ln ions. In particular, the incorporated Ln-O clusters with a nuclearity of 26 are significantly larger than known high-nuclearity (≤10) Ln-O clusters in POM chemistry. Furthermore, they also contain the largest number of La and Ce centers for any POM reported to date and represent a new kind of rare giant POMs with more than 100 W atoms. Interestingly, the La26-containing POM can undergo a single-crystal to single-crystal structural transformation in the presence of various transition-metal ions, such as Cu2+, Co2+, and Ni2+, from an inorganic molecular nanocluster into an inorganic-organic hybrid extended framework that is built from POM building blocks with even higher-nuclearity La28 clusters bridged by transition-metal complexes. [ABSTRACT FROM AUTHOR]

The first series of niobium-tungsten-lanthanide (Nb-W-Ln) heterometallic polyoxometalates {Ln12W12O36(H2O)24(Nb6O19)12} (Ln=Y, La, Sm, Eu, Yb) have been obtained, which are comprised of giant cluster-in-cluster-like ({Ln12W12}-in-{Nb72}) structures built from 12 hexaniobate {Nb6O19} clusters gathered together by a rare 24-nuclearity sodalite-type heterometal-oxide cage {Ln12W12O36(H2O)24}. The Nb-W-Ln clusters present the largest multi-metal polyoxoniobates and a series of rare high-nuclearity 4d-5d-4f multicomponent clusters. Furthermore, the giant Nb-W-Ln clusters may be isolated as discrete inorganic alkali salts and can be used as building blocks to form high-dimensional inorganic-organic hybrid frameworks. [ABSTRACT FROM AUTHOR]

A series containing the highest nuclearity polyoxoniobate (PONb) nanoclusters, ranging from dimers to tetramers, has been obtained. They include one 114-nuclear {Li8⊂Nb114O316}, one 81-nuclear {Li3K⊂Nb81O225}, and one 52-nuclear {H4Nb52O150}. The Nb nuclearity of these PONbs is remarkably larger than those of all known high-nuclearity PONbs (≤32). Furthermore, the introduction of 3d Cu2+ ions can lead to the generation of extended inorganic-organic hybrid frameworks built from novel, high-nuclearity, nanoscale heterometallic PONb building blocks {H3Cu3Nb78O222} or {H3Cu4(en)Nb78O222}. These building blocks also contain the largest number of Nb centers of any heterometallic PONbs reported to date. The synthesis of new-type PONbs has long been a challenging subject in PONb chemistry. [ABSTRACT FROM AUTHOR]

A series of Nb-W-Ln heterometallic polyoxometalates {Ln12W12O36(H2O)24 (Nb6O19)12} (Ln: Y, La, Sm, Eu, Yb) is prepared by e.g. hydrothermal reaction of K7HNb6O19, Na2WO4, Cu(OAc)2, SmCl3, trimesic acid, and en in a carbonate buffer at pH 10.5 (autoclave, 160 °C, 72 h, 70% yield). [ABSTRACT FROM AUTHOR]