Structure Transformation of Methylammonium Polyoxomolybdates via In-Solution Acidification and Solid-State Heating from Methylammonium Monomolybdate and Application as Negative Staining Reagents for Coronavirus Observation.

We prepared polyoxomolybdates with methylammonium countercations from methylammonium monomolybdate, (CH3NH3)2[MoO4], through two dehydrative condensation methods, acidifying in the aqueous solution and solid-state heating. Discrete (CH3NH3)10[Mo36O112(OH)2(H2O)14], polymeric ((CH3NH3)8[Mo36O112(H2O)14])n, and polymeric ((CH3NH3)4[γ-Mo8O26])n were selectively isolated via pH control of the aqueous (CH3NH3)2[MoO4] solution. The H2SO4-acidified solution of pH < 1 produced "sulfonated α-MoO3", polymeric ((CH3NH3)2[(MoO3)3(SO4)])n. The solid-state heating of (CH3NH3)2[MoO4] in air released methylamine and water to produce several methylammonium polyoxomolybdates in the sequence of discrete (CH3NH3)8[Mo7O24-MoO4], discrete (CH3NH3)6[Mo7O24], discrete (CH3NH3)8[Mo10O34], and polymeric ((CH3NH3)4[γ-Mo8O26])n, before their transformation into molybdenum oxides such as hexagonal-MoO3 and α-MoO3. Notably, some of their polyoxomolybdate structures were different from polyoxomolybdates produced from ammonium molybdates, such as (NH4)2[MoO4] or (NH4)6[Mo7O24], indicating that countercation affected the polyoxomolybdate structure. Moreover, among the tested polyoxomolybdates, (CH3NH3)6[Mo7O24] was the best negative staining reagent for the observation of the SARS-CoV-2 virus using transmission electron microscopy.

A Cationic Metal Glue Strategy for Expanding Paramagnetic Hetero-Multinuclear Metal-Oxo Clusters within Polyoxometalate Ligands.

Precise structural design of large hetero-multinuclear metal-oxo clusters is crucial for controlling their large spin ground states and multielectron redox properties for application as a single-molecule magnet (SMM), molecular magnetic refrigeration, and efficient redox catalyst. However, it is difficult to synthesize large hetero-multinuclear metal oxo clusters as designed because the final structures are unpredictable when employing conventional one-step condensation reaction of metal cations and ligands. Herein, we report a "cationic metal glue strategy" for increasing the size and nuclearity of hetero-multinuclear metal-oxo clusters by using lacunary-type anionic molecular metal oxides (polyoxometalates, POMs) as rigid multidentate ligands. The employed method enabled the synthesis of {(FeMn4 )Mn2 Ln2 (FeMn4 )} oxo clusters (Ln=Gd, Tb, Dy, and Lu), which are the largest among previously reported paramagnetic hetero-multinuclear metal-oxo clusters in POMs and showed unique SMM properties. These clusters were synthesized by conjugating {FeMn4 } oxo clusters with Mn and Ln cations as glues in a predictable way, indicating that the "cationic metal glue strategy" would be a powerful tool to construct desired large hetero-multinuclear metal clusters precisely and effectively.

Effective Storage of Electrons in Water by the Formation of Highly Reduced Polyoxometalate Clusters.

Aqueous solutions of polyoxometalates (POMs) have been shown to have potential as high-capacity energy storage materials due to their potential for multi-electron redox processes, yet the mechanism of reduction and practical limits are currently unknown. Herein, we explore the mechanism of multi-electron redox processes that allow the highly reduced POM clusters of the form {MO3}y to absorb y electrons in aqueous solution, focusing mechanistically on the Wells-Dawson structure X6[P2W18O62], which comprises 18 metal centers and can uptake up to 18 electrons reversibly (y = 18) per cluster in aqueous solution when the countercations are lithium. This unconventional redox activity is rationalized by density functional theory, molecular dynamics simulations, UV-vis, electron paramagnetic resonance spectroscopy, and small-angle X-ray scattering spectra. These data point to a new phenomenon showing that cluster protonation and aggregation allow the formation of highly electron-rich meta-stable systems in aqueous solution, which produce H2 when the solution is diluted. Finally, we show that this understanding is transferrable to other salts of [P5W30O110]15- and [P8W48O184]40- anions, which can be charged to 23 and 27 electrons per cluster, respectively.

Robotic Stepwise Synthesis of Hetero-Multinuclear Metal Oxo Clusters as Single-Molecule Magnets.

An efficient stepwise synthesis method for discovering new heteromultinuclear metal clusters using a robotic workflow is developed where numerous reaction conditions for constructing heteromultinuclear metal oxo clusters in polyoxometalates (POMs) were explored using a custom-built automated platform. As a result, new nonanuclear tetrametallic oxo clusters {FeMn4}Lu2A2 in TBA5[(A-α-SiW9O34)2FeMn4O2{Lu(acac)2}2A2] (IIA; A = Ag, Na, K; TBA = tetra-n-butylammonium; acac = acetylacetonate) were discovered by the installation of diamagnetic metal cations A+ into a paramagnetic {FeMn4}Lu2 unit in TBA7[(A-α-SiW9O34)2FeMn4O2{Lu(acac)2}2] (I). POMs IIA exhibited single-molecule magnet properties with the higher energy barriers for magnetization reversal (IIAg, 40.0 K; IINa, 40.3 K; IIK, 26.7 K) compared with that of the parent I (19.7 K). Importantly, these clusters with unique properties were constructed as designed by a step of the predictable sequential multistep reactions with the time-efficient platform.

Effect of Heteroatoms on Field-Induced Slow Magnetic Relaxation of Mononuclear FeIII ( S = 5/2) Ions within Polyoxometalates.

In this paper, the synthesis and magnetic properties of mononuclear FeIII-containing polyoxometalates (POMs) with different types of heteroatoms, TBA7H10[(A-α-XW9O34)2Fe] (IIX, X = Ge, Si; TBA = tetra- n-butylammonium), are reported. In these POMs, mononuclear highly distorted six-coordinate octahedral [FeO6]9- units are sandwiched by two trivacant lacunary units [A-α-XW9O34]10- (X = Ge, Si). These POMs exhibit field-induced slow magnetic relaxation based on the single high-spin FeIII magnetic center ( S = 5/2). Combining experiment and ab initio calculations, we investigated the effect of heteroatoms of the lacunary units on the field-induced slow magnetic relaxation of these POMs. By changing the heteroatoms from Si (IISi) to Ge (IIGe), the coordination geometry around the FeIII ion is mildly changed. Concretely, the axial Fe-O bond length in IIGe is shortened compared with that in IISi, and consequently the distortion of the [FeO6]9- unit in IIGe from the ideal octahedral coordination geometry becomes larger than that in IISi. The effective demagnetization barrier of IIGe (11.4 K) is slightly larger than that of IISi (9.2 K). Multireference ab initio calculations predict zero-field splitting parameters in good agreement with experiment. Although the differences in the coordination geometries and magnetic properties of IIGe and IISi are quite small, ab initio calculations indicate subtle changes in the magnetic anisotropy which are in line with the observed magnetic relaxation properties.

Alkoxides of Trivacant Lacunary Polyoxometalates.

Lacunary polyoxometalates (POMs) are useful rigid multidentate inorganic ligands to construct multinuclear metal oxo clusters and inorganic-organic hybrid materials. However, the use of multivacant lacunary POMs often suffers from their undesired condensation reactions at the highly reactive vacant sites. Herein, the introduction of alkoxy protecting groups into the vacant sites of lacunary POMs in organic media is reported for the first time. By reacting organic solvent-soluble trivacant lacunary Keggin-type POMs with methanol, six methoxy groups were successfully introduced into the vacant sites, resulting in the formation of the alkoxides TBA4 [A-α-XW9 O28 (OCH3 )6 ] (Ix -OMe; X=Si, Ge). These methoxy groups could protect the reactive vacant sites and suppress the undesired dimerization reaction into the corresponding α-Dawson-type POMs. Since the introduced monodentate methoxy groups could easily be dissociated by hydrolysis, ISi -OMe could be utilized as the precursor for the synthesis of metal-substituted POMs. In addition, by using pentaerythritol as the multidentate alkoxy ligand, the monomeric alkoxide TBA4 [A-α-SiW9 O28 {(OCH2 )2 C(CH2 OH)2 }3 ] (ISi -PE) was successfully synthesized. In particular, these multidentate alkoxy groups showed high resistance against hydrolysis. Moreover, by reacting ISi -PE with trivacant lacunary Keggin-type POMs, the dimeric inorganic-organic-inorganic hybrid structures TBAn H8-n [(A-α-SiW9 O28 ){(OCH2 )2 C(CH2 O)2 }3 (A-α-XW9 O28 )] (IISiX -PE; X=Si, Ge) with the same or different heteroatoms (Si and Ge) were successfully synthesized.

Sequential Synthesis of 3d-3d'-4f Heterometallic Heptanuclear Clusters in between Lacunary Polyoxometalates.

In this work, we have successfully created several unprecedented discrete 3d-3d'-4f heterotrimetallic clusters in between lacunary polyoxometalates (POMs). By the three-step sequential introduction of metal cations into a trivacant lacunary POM TBA4H6[A-α-SiW9O34] (TBA = tetra-n-butylammonium) in organic media, five kinds of sandwich-type POMs with double-diamond-shaped 3d-3d'-4f heptanuclear clusters (IIIFeM4Ln2, TBAnHm[FeM4{Ln(L)2}2O2(A-α-SiW9O34)2], M = Mn(3+), Cu(2+); Ln = Gd(3+), Dy(3+), Lu(3+); L = acac (acetylacetonate), hfac (hexafluoroacetylacetonate)) were successfully synthesized for the first time. By introduction of two [Ln(L)2](+) units on the ends of pentanuclear clusters [FeMn4O18(OH)2](23-) and [FeCu4O18(OH)2](27-), the magnetic interactions between Mn(3+)-Mn(3+) and Cu(2+)-Cu(2+) could be modulated. Among a series of the heterometallic heptanuclear compounds, IIIFeMn4Lu2 exhibited the slow magnetic relaxation characteristic for a single-molecule magnet under the zero applied magnetic fields.

Synthesis and Disassembly/Reassembly of Giant Ring-Shaped Polyoxotungstate Oligomers.

The disassembly and reassembly of giant molecules are essential processes in controlling the structure and function of biological and artificial systems. In this work, the disassembly and reassembly of a giant ring-shaped polyoxometalate (POM) without isomerization of the monomeric units is reported. The reaction of a hexavacant lacunary POM that is soluble in organic solvents, [P2 W12 O48 ](14-) , with manganese cations gave the giant ring-shaped POM [{γ-P2 W12 O48 Mn4 (C5 H7 O2 )2 (CH3 CO2 )}6 ](42-) . This POM is a hexamer of manganese-substituted {P2 W12 O48 Mn4 } units, and its inner cavity was larger than any of those previously reported for ring-shaped polyoxotungstates. It was disassembled into monomeric units in acetonitrile, and the removal of the capping organic ligands on the manganese cations led to reassembly into a tetrameric ring-shaped POM, [{γ-P2 W12 O48 Mn4 (H2 O)6 }4 (H2 O)4 ](24-) .

Synthesis of α-Dawson-type silicotungstate [α-Si2W18O62]8- and protonation and deprotonation inside the aperture through intramolecular hydrogen bonds.

The design of structurally well-defined anionic molecular metal-oxygen clusters, polyoxometalates (POMs), leads to inorganic receptors with unique and tunable properties. Herein, an α-Dawson-type silicotungstate, TBA8[α-Si2W18O62]⋅3 H2O (II) that possesses a -8 charge was successfully synthesized by dimerization of a trivacant lacunary α-Keggin-type silicotungstate TBA4H6[α-SiW9O34]⋅2 H2O (I) in an organic solvent. POM II could be reversibly protonated (in the presence of acid) and deprotonated (in the presence of base) inside the aperture by means of intramolecular hydrogen bonds with retention of the POM structure. In contrast, the aperture of phosphorus-centered POM TBA6[α-P2W18O62]⋅H2O (III) was not protonated inside the aperture. The density functional theory (DFT) calculations revealed that the basicities and charges of internal µ3-oxygen atoms were increased by changing the central heteroatoms from P(5+) to Si(4+), thereby supporting the protonation of II. Additionally, II showed much higher catalytic performance for the Knoevenagel condensation of ethyl cyanoacetate with benzaldehyde than I and III.

Synthesis Strategies and Structures of Molecular Heterometallic Oxo Clusters.

Multinuclear heterometallic oxo clusters, composed of two or more different metal cations bridged by oxo ligands, represent an important class of molecular complexes known for their unique magnetic, catalytic, and electrochemical properties resulting from cooperative interactions between the metal cations. If three or more types of metal cations can be arranged as designed, their chemical and physical properties can be precisely and flexibly controlled, potentially creating innovative materials. However, research on hetero-trimetallic and hetero-tetrametallic oxo clusters remains limited. This review presents an interdisciplinary search of multinuclear heterometallic oxo clusters, regardless of the type of ligand, to explain and classify their synthesis strategies and structures. By cataloging crystallographically characterized heterometallic oxo clusters using ligand-per-metal values and synthesis method notations, valuable insights have been gained into effective synthesis methods for the precise arrangement of metal cations. The advantages and disadvantages of one-pot synthesis methods and synthesis strategies for achieving precise structural control of heterometallic oxo clusters are discussed with an emphasis on the prediction of their final structures. The insights from this review are expected to drive the development of synthetic and analytical techniques for the precise synthesis of heterometallic complexes in a predictable way.

Disassembly and reassembly of the non-conventional thermophilic C-phycocyanin.

C-phycocyanin (CPC), which contains open-chain tetrapyrroles, is a major light-harvesting red-fluorescent protein with an important role in aquatic photosynthesis. Recently, we reported a non-conventional CPC from Thermoleptolyngbya sp. O-77 (CPCO77) that contains two different structures, i.e., a hexameric structure and a non-conventional octameric structure. However, the assembly and disassembly mechanisms of the non-conventional octameric form of CPC remain unclear. To understand this assembly mechanism, we performed an in vitro experiment to study the disassembly and reassembly behaviors of CPC using isolated CPC subunits. The dissociation of the CPCO77 subunit was performed using a Phenyl-Sepharose column in 20 mM potassium phosphate buffer (pH 6.0) containing 7.0 M urea. For the first time, crystals of isolated CPC subunits were obtained and analyzed after separation. After the removal of urea from the purified α and ß subunits, we performed an in vitro reassembly experiment for CPC and analyzed the reconstructed CPC using spectrophotometric and X-ray crystal structure analyses. The crystal structure of the reassembled CPC was nearly identical to that of the original CPCO77. The findings of this study indicate that the octameric CPCO77 is a naturally occurring form in the thermophilic cyanobacterium Thermoleptolyngbya sp. O-77.

Selective formate production from H2 and CO2 using encapsulated whole-cells under mild reaction conditions.

Biocatalytic CO2 reduction into formate is a crucial strategy for developing clean energy because formate is considered as one of the promising hydrogen storage materials for achieving net-zero carbon emissions. Here, we developed an efficient biocatalytic system to produce formate selectively by coupling two enzymatic activities of H2 oxidation and CO2 reduction using encapsulated bacterial cells of Citrobacter sp. S-77. The encapsulated whole-cell catalyst was made by living cells depositing into polyvinyl alcohol and gellan gum cross-linked by calcium ions to form hydrogel beads. Formate production using encapsulated cells was carried out under the resting state conditions in the gas mixture of H2/CO2 (70:30, v/v%). The whole-cell biocatalyst showed highly efficient and selective catalytic production of formate, reaching the specific rate of formate production of 110 mmol L-1· gprotein-1·h-1 at 30 °C, pH 7.0, and 0.1 MPa. The encapsulated cells can be reused at least 8 times while keeping their high catalytic activities for formate production under mild reaction conditions.

Non-conventional octameric structure of C-phycocyanin.

C-phycocyanin (CPC), a blue pigment protein, is an indispensable component of giant phycobilisomes, which are light-harvesting antenna complexes in cyanobacteria that transfer energy efficiently to photosystems I and II. X-ray crystallographic and electron microscopy (EM) analyses have revealed the structure of CPC to be a closed toroidal hexamer by assembling two trimers. In this study, the structural characterization of non-conventional octameric CPC is reported for the first time. Analyses of the crystal and cryogenic EM structures of the native CPC from filamentous thermophilic cyanobacterium Thermoleptolyngbya sp. O-77 unexpectedly illustrated the coexistence of conventional hexamer and novel octamer. In addition, an unusual dimeric state, observed via analytical ultracentrifugation, was postulated to be a key intermediate structure in the assemble of the previously unobserved octamer. These observations provide new insights into the assembly processes of CPCs and the mechanism of energy transfer in the light-harvesting complexes.

Biochemical and structural characterization of a thermostable Dps protein with His-type ferroxidase centers and outer metal-binding sites.

The DNA-binding protein from starved cells (Dps) is found in a wide range of microorganisms, and it has been well characterized. However, little is known about Dps proteins from nonheterocystous filamentous cyanobacteria. In this study, a Dps protein from the thermophilic nonheterocystous filamentous cyanobacterium Thermoleptolyngbya sp. O-77 (TlDps1) was purified and characterized. PAGE and CD analyses of TlDps1 demonstrated that it had higher thermostability than previously reported Dps proteins. X-ray crystallographic analysis revealed that TlDps1 possessed His-type ferroxidase centers within the cavity and unique metal-binding sites located on the surface of the protein, which presumably contributed to its exceedingly high thermostability.

Homogeneous catalytic reduction of polyoxometalate by hydrogen gas with a hydrogenase model complex.

The homogeneous catalytic reduction of a polyoxometalate (POM) by hydrogen gas in aqueous media was investigated for the first time by using a [NiRu] hydrogenase model complex (I) under very mild conditions. By bubbling hydrogen gas into the buffer solution containing I and the Dawson-type POM (IIox), the color of the solution turned from pale yellow to dark blue, suggesting the reduction of IIox. The catalytic and kinetic studies revealed that I acted as an efficient catalyst to yield one-electron-reduced Dawson-type POM (IIred) with a low energy barrier for activating dihydrogen and reducing IIox via a hydride complex of I. The process for the one-electron reduction of IIox was confirmed by UV-vis spectroscopy, controlled potential electrolysis, and X-ray photoelectron spectroscopy. POM IIred could stably store protons and electrons and release them by addition of oxidants, demonstrating that POMs acted as redox active mediators for transporting protons and electrons from hydrogen gas to acceptors. The recycle study showed that IIox and IIred could be reduced and oxidized by hydrogen and oxygen gases, respectively, at least five times with >99% yield of reduced species, showing a durable system for extracting protons and electrons from hydrogen gas.

Hexavacant γ-Dawson-type phosphotungstates supporting an edge-sharing bis(square-pyramidal) {O2M(µ3-O)2(µ-OAc)MO2} core (M = Mn2+, Co2+, Ni2+, Cu2+, or Zn2+).

In aqueous media, the introduction of additional metal species into polyoxometalates (POMs) with multiple vacant sites, such as a hexavacant Dawson-type phosphotungstate, which is of interest for the synthesis of novel metal oxide clusters, is generally difficult because they easily undergo self-condensation and/or structural decomposition. In this study, we succeeded in developing a novel synthetic method to obtain metal-substituted γ-Dawson-type phosphotungstate monomers by introducing metal species into an organic solvent-soluble lacunary phosphotungstate, TBA4H10[α-P2W12O48] (I) (TBA = tetra-n-butylammonium), in organic media. The reaction of I, which possessed two types of vacant sites, i.e. middle and edge sites, with divalent metal species such as Mn2+, Co2+, Ni2+, Cu2+, or Zn2+ in acetonitrile afforded a series of isostructural POMs M2 (TBA5[γ-P2W12O44M2(OAc)(CH3CONH)2]·nH2O·mCH3CN; M = Mn2+, Co2+, Ni2+, Cu2+, or Zn2+; OAc = acetate) with an edge-sharing bis(square-pyramidal) {O2M(µ3-O)2(µ-OAc)MO2} core. The bis(square-pyramidal) core was selectively placed at the middle site of the hexavacant lacunary phosphotungstate, and the two metals in the core were bridged by two phosphate units and one acetate species. Meanwhile, the edge sites were capped by acetimidate ligands, which protect the reactive lacunary POM from self-condensation. To the best of our knowledge, this is the first report describing the synthesis and characterization of metal-substituted hexavacant γ-Dawson-type POM monomers.

A modular synthesis approach to multinuclear heterometallic oxo clusters in polyoxometalates.

We report a "modular synthesis approach" to multinuclear heterometallic oxo clusters in lacunary polyoxometalates (POMs). This approach allowed the synthesis of a POM containing a nonanuclear {CrMn4}Lu2Ag2 cluster with the widest variety of metals among the discrete metal oxo clusters prepared to date.

Hexanuclear tin(ii) and mixed valence tin(ii,iv) oxide clusters within polyoxometalates.

A hexanuclear mixed valence tin oxide cluster [Sn3(2+)Sn3(4+)O15](12-) was successfully synthesized by the solution-state selective oxidation of a tin oxide cluster [Sn6(2+)O12](12-) within trivacant lacunary polyoxometalates, where lone pairs on the Sn(2+) species acted as stereochemically active sites.

A cascade approach to hetero-pentanuclear manganese-oxide clusters in polyoxometalates and their single-molecule magnet properties.

Structurally well-defined hetero-pentanuclear manganese-oxide clusters {MMn4} were successfully synthesized in TBA7Hn[MMn4(OH)2(A-α-SiW9O34)2]·2H2O·C2H4Cl2 (, M = Fe(iii), Co(ii), Ni(ii), Cu(ii), Ga(iii)) by sequential introduction of metal cations into the trivacant lacunary polyoxometalates (POMs). The pentanuclear manganese-oxide cluster {Mn5} showed a small spin ground state and a low energy barrier for magnetization relaxation. In contrast, the magnetic interactions in the hetero-pentanuclear clusters could be controlled by the arrangements of metals, and the clusters showed large magnetic anisotropy and single-molecule magnet behavior. In particular, the cluster {FeMn4} in (S = 11/2) showed the slowest relaxation and the highest energy barrier among the previously reported transition metal-containing POMs.