Inorganic Clusters Research Articles

Macrocyclic Inorganic Tin-Containing Oxo Clusters: Heterometallic Strategy for Configuration and Catalytic Activity Modulation.

In this work, the first examples of inorganic macrocyclic tin-oxo clusters which are stabilized by sulfate ligands are reported. As determined by X-ray diffraction and photoelectron spectroscopy analyses, the prepared inorganic Sn10 -oxo cluster displays interesting mixed valence behaviors, with 8 Sn4+ located at the cyclic skeleton and two Sn2+ encapsulated in the center. When further introducing Ti4+ and In3+ ions to the synthetic systems, heterometallic Sn2 Ti6 and SnIn5 Ti6 complexes with Ti6 (SO4 )9 and SnIn5 (SO4 )12 macrocyclic skeletons were prepared whose configuration and packing models were affected by the ionic radius of incorporated metals. Moreover, comparative CO2 reduction experiments confirm that such heterometallic composition can significantly improve the catalytic activities of these inorganic macrocyclic oxo clusters. This work represents a milestone in constructing inorganic tin complexes and also macrocyclic metal oxo clusters with tunable configurations and properties.

Precise Construction of Stable Bimetallic Metal–Organic Frameworks with Single-Site Ti(IV) Incorporation in Nodes for Efficient Photocatalytic Oxygen Evolution

Precise Construction of Stable Bimetallic Metal–Organic Frameworks with Single-Site Ti(IV) Incorporation in Nodes for Efficient Photocatalytic Oxygen Evolution

Single-Crystal-to-Single-Crystal Cluster Transformation in a Microporous Molybdoarsenate(V)-Metalorganic Framework.

The hybrid compound [Cu(cyclam)(H2O)2]0.5[{Cu(cyclam)}1.5{B-H2As2Mo6O26(H2O)}]·9H2O (1) (cyclam = 1,4,8,11-tetraazacyclotetradecane) was synthesized in aqueous solution by reacting the {Cu(cyclam)}2+ complex with a mixture of heptamolybdate and an arsenate(V) source. Crystal packing of 1 exhibits a supramolecular open-framework built of discrete covalent molybdoarsenate/metalorganic units and additional [Cu(cyclam)(H2O)2]2+ cations, the stacking of which generates squarelike channels parallel to the z axis with an approximate cross section of 10 × 11 Å2 where all the hydration water molecules are hosted. Thermal evacuation of solvent molecules yields a new anhydrous crystalline phase, but compound 1 does not preserve its single-crystalline nature upon heating. However, when crystals are dehydrated under vacuum, they undergo a structural transformation that proceeds via a single-crystal-to-single-crystal pathway, leading to the anhydrous phase [{Cu(cyclam)}2(A-H2As2Mo6O26)] (2). Total dehydration results in important modifications within the inorganic cluster skeleton which reveals an unprecedented solid-state B to A isomerization of the polyoxoanion. This transition also involves changes in the CuII bonding scheme that lead to covalent cluster/metalorganic layers by retaining the open-framework nature of 1. Compound 2 adsorbs ambient moisture upon air exposure, but it does not revert back to 1, and the hydrated phase [{Cu(cyclam)}2(A-H2As2Mo6O26)]·6H2O (2h) is obtained instead. Structural variations between 1 and 2 are reflected in electron paramagnetic resonance spectroscopy measurements, and the permanent microporosity of 2 provides interesting functionalities to the system such as the selective adsorption of gaseous CO2 over N2.

Rhenium – A Tuneable Player in Tailored Hydrogenation Catalysis

AbstractAlthough rhenium may not be the most common choice of active species in catalysis, it has been reported as a highly active and selective catalyst over a wide range of reactions. Its applications include hydrogenation reactions of great relevance in the field of renewable materials and bio‐derived platform molecules, such as valorization of lignin, CO2, and carboxylic acids. Different from several transition metals, rhenium presents oxidation numbers varying from −3 to +7. Such diversity in the coordination chemistry of rhenium is reflected in the variety of known rhenium compounds, since this metal can form stable structures such as ligand‐bridged multinuclear and organometallic compounds as well as inorganic oxides, metal‐organic frameworks, and clusters. The exceptional flexibility in rhenium speciation yields numerous selective catalysts; however, it also makes the characterization of rhenium catalysts challenging, and its influence on the catalytic activity is not trivial. This review will outline the most established rhenium‐based materials used in hydrogenation catalysis and shed some light on the relation of rhenium species to catalyst selectivity based on advanced characterization techniques. Finally, our perspectives on the use of rhenium catalysts to produce value‐added products will be given.

Towards purely inorganic clusters in medicine: Biocompatible divalent cations as counterions of cobaltabis(dicarbollide) and its iodinated derivatives

Monovalent cations, Cs+, and alkylammonium ([NR4]+) salts have traditionally been used to precipitate the anions of boranes, carborane and metallocarborane clusters. In contrast, in the body and in living organisms in general, divalent cations have a special relevance. In this work, we isolate for the first time the cobaltabis(dicarbollide) salts of the biocompatible divalent cations of biological importance that can have application both in biology and in materials science. The preparation of Ca2+, Mg2+ and Fe2+ salts of anionic iodinated nido-[C2B9H12]− and cobaltabis(dicarbollide) as well as its di-, tetra- and octa-iodinated derivatives are reported. Ca2+ and Mg2+ are hard Lewis acids and thus forms aqua ions if water is present in the synthetic process. All solid Ca2+ and Mg2+ salts studied in this work contained water molecules coordinated that have been detected by IR and TGA/DSC. Fe2+ is a medium hard Lewis acid and Fe3+ is a hard one. In acetone they do not coordinate to cobaltabis(dicarbollide) anion, but are solvated by acetone. The studied Ca2+ salts of iodinated cobaltabis(dicarbollide) are basically inorganic small molecules that provide at once the biocompatible divalent Ca2+ cation and and iodinated anions thus simultaneously providing an X-ray contrast agent and/or bone defect repairing agent in regenerative medicine.

Constructing π-Stacked Supramolecular Cage Based Hierarchical Self-Assemblies via π···π Stacking and Hydrogen Bonding.

Constructing supramolecular cages with multiple subunits via weak intermolecular interactions is a long-standing challenge in chemistry. So far, π-stacked supramolecular cages still remain unexplored. Here, we report a series of π-stacked cage based hierarchical self-assemblies. The π-stacked cage (π-MX-cage) is assembled from 16 [MXL]+ ions (M = Mn2+, Co2+; X = Br-, SCN-, Cl-; and L = tris(2-benzimidazolylmethyl)amine) via 18 intermolecular π-stacking interactions. The tetrahedral cage, consisting of four [MXL]+ ions as the vertexes and six pairs of [MXL]+ ions as the edges, features 48 exterior N-H hydrogen bond donors for hydrogen bond formation with guest molecules. By variation of the M2+/X- pair, the π-MX-cage demonstrates unique versatility for incorporating a wide variety of species via different hydrogen-bonding modes during the assembly of hierarchical superstructures. In specific, the π-MnBr-cages encapsulate acetonitrile (CH3CN) or cis-1,3,5-cyclohexanetricarbonitrile (cis-HTN) molecules in the central voids, while a core-shell tetrahedral inorganic cluster [Mn(H2O)6]@([Mn(H2O)4]4[Br42-]6) (Mn@Mn4-cage) is captured within the interstitial regions between cages. The π-CoSCN-cages are capable of stabilizing reactive sulfur-containing species, such as S2O42-, S2O62-, and HSO3- ions, in the hierarchical superstructure. Finally, H2PO4- ions are incorporated between π-CoCl-cages, resulting in an inorganic mesoporous framework. These results provide insights into further exploring the chemistry and hierarchical assembly of supramolecular cages based on π-π stacking intermolecular interactions.

A Purely Inorganic Quasi-Keggin Polyoxometalate for Photocatalytic Conversion of Carbon Dioxide to Carbon Monoxide.

A pure inorganic cluster, H47 Na2 Co4 Mo24 (PO4 )11 O72 ⋅ 15H2 O (denoted as {Co4 Mo24 }), has been successfully synthesized by hydrothermal method. Notably, the assembly of a central {Co2 PO4 } tetrahedron and four peripheral {Co[P4 Mo6 ]} fragments gives rise to a rare "quasi-Keggin" structure of {Co4 Mo24 }, in which Co linkers continue to bridge adjacent substructures, resulting in the generation of 3D framework with large cavities. Benefitting from the combination of strong reductive {P4 Mo6 } units and Co active centers, the photocatalytic system with {Co4 Mo24 } as heterogeneous catalyst exhibits excellent activity for CO2 conversion to CO, offering the CO formation rate of 1848.3 μmol g-1 h-1 with high selectivity of 97.0 %. Besides, thermogravimetric and X-ray diffraction analysis confirm that {Co4 Mo24 } can maintain stable during the photocatalytic reaction process.

Highly Soluble Supertetrahedra upon Selective Partial Butylation of Chalcogenido Metalate Clusters in Ionic Liquids

AbstractSupertetrahedral clusters have been reported in two generally different types so far: one type possessing an organic ligand shell, no or low charges, and high solubility, while the other cluster type is ligand‐free with usually high charges and low or no solubility in common solvents. The latter is a tremendous disadvantage regarding further use of the clusters in solution. However, as organic substituents usually broaden the HOMO–LUMO gaps, which cannot be overcompensated by the (limited) cluster sizes, a full organic shielding comes along with drawbacks regarding opto‐electronic properties. We therefore sought to find a way of generating soluble clusters with a minimum number of organic substituents. Here, we present the synthesis and full characterization of two salts of [Sn10O4S16(SBu)4]4− that are high soluble in CH2Cl2 or CH3CN, which includes first NMR and mass spectra obtained from solutions of such salts with mostly inorganic supertetrahedral clusters. The optical absorption properties of this new class of compounds indicates nearly unaffected band gaps. The synthetic approach and the spectroscopic findings were rationalized and explained by means of high‐level quantum chemical studies.

Self-Assembled Polyoxometalate Nanodots as Bidirectional Cluster Catalysts for Polysulfide/Sulfide Redox Conversion in Lithium-Sulfur Batteries.

Polyoxometalates (POMs) are a class of discrete molecular inorganic metal-oxide clusters with reversible multielectron redox capability. Taking advantage of their redox properties, POMs are thus expected to be directly involved in the lithium-sulfur batteries (Li-S, LSBs) system as a bidirectional molecular catalyst. Herein, we design a three-dimensional porous structure of reduced graphene-carbon nanotube skeleton supported POM catalyst as a high-conductive and high-stability host material. Based on various spectroscopic techniques and in situ electrochemical studies together with computational methods, the catalytic mechanism of POM clusters in Li-S battery was systematically clarified at the molecular level. The constructed POM-based sulfur cathode delivers a reversible capacity 1110 mAh g-1 at 1.0 C and cycling stability up to 1000 cycles at 3.0 C. Furthermore, Li-S pouch/beaker batteries with a POM-based cathode were successfully demonstrated. This work provides essential inputs to promote molecular catalyst design and its application in LSBs.

Polyoxometalates in Extraction and Sorption Processes

ABSTRACT Polyoxometalates (POMs) represent a fascinating class of inorganic cluster compounds. Due to the almost unlimited possibilities to tailor size, shape and charge of this compound class and to perform various surface functionalization, they are discussed for different applications, especially in the fields of catalysis, material sciences, and biomedicine. In contrast, the systematic study of extraction and sorption properties of POMs has received relatively little attention so far. This review article provides a brief overview of relevant POM structures used for effective and selective phase transfer of metal ions from aqueous into organic media as well as for the development of efficient sorption processes. The use of inorganic-organic POM-based hybrid materials for extraction and sorption processes is also discussed.

Projector-Free Capped-Fragment Scheme within Density Functional Embedding Theory for Covalent and Ionic Compounds.

Quantum-mechanics-(QM)-based simulations now routinely aid in understanding and even discovering new chemistries involving molecules and materials exhibiting desired functionalities. Ab initio correlated wavefunction (CW) theories systematically improve QM methods, with many exhibiting high accuracy. However, execution of CW methods requires expensive computations that typically scale poorly with system size. Divide-and-conquer approaches partition large systems into smaller fragments; a lower level of theory treats fragment interactions while a preferred higher level of theory describes the important fragment. These methods offer ways to incorporate CWs into chemical simulations of large systems, e.g., biomolecules, surfaces, large inorganic clusters, bulk crystals, etc. Here we propose a partitioning protocol that utilizes capping atoms to saturate severed covalent bonds at fragment interfaces and density functional embedding theory (DFET) to describe fragment interactions. The capping groups in each fragment provide an ad-hoc potential that approximates the effects of the environment. An embedding potential optimized via DFET then serves as an augmentation of the capping group to simulate the effects of the environment. We concurrently use an auxiliary fragment (a separate system comprised of only the combined capping groups) to account for, and thereby correct, the electron density contributions of all the capping groups added to all of the fragments. This method depends only on the capped-subsystem and auxiliary-fragment electron densities, forgoing, as with the original DFET developed for metallic systems, orbital-based projector approaches that determine a nonlocal action of the embedding potential onto the fragment electrons. By using an auxiliary fragment, the method maintains a purely electron-density-dependent embedding potential, substantially lessening the cost and leading to simpler implementation. Here, we demonstrate the utility of our capped-DFET and ensuing capped embedded CW method in two contrasting systems, namely, an organic molecule and an ionic metal oxide cluster.

Dip Coating From Density Mismatching Mixture

Abstract Solid transfer technology from mixtures is gaining ever-increasing attention from materials scientists and production engineers due to their high potential in near-net-shaped production of cost-effective engineering components. Dip coating, a wet deposition method, is an effective and straightforward way of thin-film/layers formation. The dipping mixtures are often embedded with inorganic fillers, nanoparticles, or clusters (d < 30 nm) that produce a thin film ranging from nm to couple microns. An increase in the volume of solid transfer by the dipping process can open-up a novel three-dimensional near-net-shape production. However, adding a larger inorganic particle size (>1 μm) or adding a higher solid fraction will increase the solid transfer but may result in a multiphase heterogeneous mixture. In this work, the physical mechanism of an increased volume of solid transfer with a larger spherical particle size (>5 μm) is investigated. Polymer-based glue and evaporating solvent are mixed to construct the liquid carrier system (LCS) for large inorganic hard particles. Moderate volume fraction of inorganic particles (20% < ϕp < 50%) are added into the LCS solution as solid loading. Three levels of binder volume fraction are considered simultaneously to investigate the effect of the solid transfer. Cylindrical AISI 304 steel wire with dia 0.81 mm is used as the substrate for dipping and coating. The coating thickness, weight, and surface packing coverage by the particles are measured in our lab. The results presented the influence of volume fraction of inorganic particle and glue composition on the solid transfer from the heterogeneous mixture.

Inhibitors of CA IX Enzyme Based on Polyhedral Boron Compounds

AbstractThis review describes recent progress in the design and development of inhibitors of human carbonic anhydrase IX (CA IX) based on space‐filling carborane and cobalt bis(dicarbollide) clusters. CA IX enzyme is known to play a crucial role in cancer cell proliferation and metastases. The new class of potent and selective CA IX inhibitors combines the structural motif of a bulky inorganic cluster with an alkylsulfamido or alkylsulfonamido anchor group for Zn2+ ion in the enzyme active site. Detailed structure‐activity relationship (SAR) studies of a large series containing 50 compounds uncovered structural features of the cluster‐containing inhibitors that are important for efficient and selective inhibition of CA IX activity. Preclinical evaluation of selected compounds revealed low toxicity, favorable pharmacokinetics and ability to reduce tumor growth. Cluster‐containing inhibitors of CA IX can thus be considered as promising candidates for drug development and/or for combination therapy in boron neutron capture therapy (BNCT).

Increased in vitro Anti-HIV Activity of Caffeinium-Functionalized Polyoxometalates.

Polyoxometalates (POMs), molecular metal oxide anions, are inorganic clusters with promising antiviral activity. Herein we report increased anti‐HIV‐1 activity of a POM when electrostatically combined with organic counter‐cations. To this end, Keggin‐type cerium tungstate POMs have been combined with organic methyl‐caffeinium (Caf) cations, and their cytotoxicity, antiviral activity and mode of action have been studied. The novel compound, Caf4K[β2‐CeSiW11O39]×H2O, exhibits sub‐nanomolar antiviral activity and inhibits HIV‐1 infectivity by acting on an early step of the viral infection cycle. This work demonstrates that combination of POM anions and organic bioactive cations can be a powerful new strategy to increase antiviral activity of these inorganic compounds.

Unprecedented saturation limit achieved by inorganic polycationic cluster (Sb7Te8)5+ for light noble gases (He & Ne)

Among noble gases, Helium and Neon have smaller size, high ionization potential and low polarizability due to which these two gases exhibit weak binding affinities toward any surface. Bartlet’s discovery and subsequent similar successful discoveries of stable complexes of noble gases opened new avenues for the storage of noble gases particularly on the new surfaces and their interactions for the storage of these gases. Here, we report the adsorption of light noble gases on polycationic clusters. Our current work not only investigates the interaction behavior of He and Ne with (Sb7Te8)5+ cluster but also explores the saturation limit of the cluster for He and Ne. Stability of various complexes of He and Ne with cationic surfaces is determined by the calculation of their interaction energies which reveal that the adsorption of single and multiple atoms of noble gases at faces of double cubic cluster is comparatively more favorable than at the bond lengths. Electronic properties such as HOMO-LUMO gaps show that complexes of He and Ne are more stable electronically than that of pure cluster, because HOMO-LUMO gap of complexes are higher than the bare polycationic cluster. NCI analysis of iso-surfaces and RDG maps confirms the presence of van der Waals forces between light noble gases and polycationic clusters. Saturation studies reveal that cluster can adsorb eleven He and/or ten Ne atoms with no or minimum distortion in the geometry of cluster. The results showed that Ne has greater tendency to interact with polycationic clusters due to the large electronic cloud and polarizability value than He.

Bimetallic Coordination in Two-Dimensional Metal–Organic Framework Nanosheets Enables Highly Efficient Removal of Heavy Metal Lead (II)

Two-dimensional (2D) metal–organic frameworks (MOFs) have emerged as intriguing 2D materials because of their specific features of 2D morphology and designable skeletons, which have elicited great interest in environment remediation. In this work, 2D MOF nanosheets are fabricated via a mixed-solvent solvothermal method, and a regulation strategy of metal inorganic clusters on MOFs is used to construct two different 2D MOFs with monometallic and bimetallic coordination, that is, Ni-MOF and Ni/Cd-MOF. Binary metal coordination renders more crystal defects and vacancies in the framework; thus, compared to monometallic Ni-MOF, bimetallic Ni/Cd-MOF exhibits fewer layers (4∼5 layers), higher specific surface area, larger pore size, and higher surface electronegativity, which leads to its excellent adsorption removal for Pb2+, with higher adsorption rate and affinity, and superior adsorption capacity (950.61 mg/g, almost twice as high as that of monometallic Ni-MOF). Besides, the adsorption mechanism further confirmed that the carboxyl groups (−COO−) from organic linker on 2D MOFs serve as the main binding sites for Pb2+ coordination, and bimetallic Ni/Cd-MOF has more active −COO− sites for Pb2+ capture. Thus, the bimetallic Ni/Cd-MOF regulated by heterogeneous metal atoms shows promising application for highly efficient adsorption of heavy metal ions.

N-doped inorganic molecular clusters as a new type of hole transport material for efficient organic solar cells

<h2>Summary</h2> At present, PEDOT:PSS and MoO₃ are the most widely used hole transport layer (HTL) in organic solar cells (OSCs); however, some drawbacks still limit their practical use. In this study, we developed a facile method to enhance the conductivity of a polyoxometalate-based inorganic cluster (PIC) without sacrificing its high work function nature. An inorganic cluster HPMO:Sn with excellent hole collection ability was prepared and used as an HTL in an OSC achieving a power conversion efficiency (PCE) of 17.3%. To the best of our knowledge, the photovoltaic performances are among the best devices reported in the field. Moreover, HPMO:Sn possesses the merits of a definite and stable chemical structure and is low cost, and HPMO:Sn can be easily prepared without any post-treatment. Besides, we prove that the HPMO:Sn HTL is very compatible with blade coating, i.e., an OSC of 1.0 cm² was fabricated using a blade-coated HPMO:Sn film to attain an efficiency of 15.1%.

An Efficient ab Initio Scheme for Discovering Organic-Inorganic Hybrid Materials by Using Genetic Algorithms.

Organic-inorganic hybrid materials (OIHMs), such as methylammonium lead triiodide (MAPbI3), have a wide composition space because of the various potential combinations of organic molecules and inorganic cages. However, for unknown OHIMs, it is difficult to predict what kind of crystal structure will be stable without any experimental data. In this work, we report an efficient scheme for predicting crystal structures and phase diagrams of MA-Pb-I systems from first-principles calculations and genetic algorithms. In our scheme, OIHMs are divided into organic molecules and inorganic clusters. A pseudobinary phase diagram of MAI-PbI2 was obtained by predicting structures at each composition. These results indicated that only MAPbI3 and MA2PbI4 are stable phases, consistent with the experiments. In addition, the electronic and optical properties of the predicted structures were calculated and the solar cell performance was evaluated. Thus, our method allowed us to search for unknown OIHMs without any experimental data.

Surface Permeability of Membrane and Catalytic Performance Based on Redox-Responsive of Hybrid Hollow Polymeric Microcapsules.

“Smart” polymeric microcapsules with excellent permeability of membranes have drawn considerable attention in scientific and industrial research such as drug delivery carriers, microreactors, and artificial organelles. In this work, hybrid hollow polymeric microcapsules (HPs) containing redox-active gold-sulfide bond were prepared with bovine serum albumin, inorganic metal cluster (AuNCs), and poly(N-isopropylacrylamide) conjugates by using Pickering emulsion method. HPs were transferred from water-in-oil to water-in-water by adding PEGbis(N-succinimidylsuccinate). To achieve redox-responsive membrane, the Au-S bond units incorporated into the microcapsules’ membranes, allowed us to explore the effects of a new stimuli, that is, the redox Au-S bond breaking on the microcapsules’ membranes. The permeability of these hybrid hollow polymeric microcapsules could be sensitively tuned via adding environment-friendly hydrogen peroxide (H2O2), resulting from a fast fracture of Au-S bond. Meanwhile, AuNCs and conjugates could depart from the microcapsules, and enhance the permeability of the membrane. Based on the excellent permeability of the membrane, phosphatase was encapsuled into HPs and p-nitrophenyl phosphate as a substrate. After adding 1 × 10−2 and 1 × 10−4 M H2O2, the catalytic efficiency was nearly 4.06 and 2.22 times higher than that of HPs in the absence of H2O2, respectively. Hence, the unique redox-responsive HPs have potential applications in biocatalytic reaction, drug delivery, and materials as well as in bioscience.

From polygons to polyhedra through intermediate structures. A shape measures study of six-atom inorganic rings and clusters.

Among the wealth of well-established molecular structures, inorganic rings and clusters present an overwhelming variety of geometries that chemists try to describe with a limited assortment of regular polygons and polyhedra. In the case of six-atom structures we usually employ the hexagon, the pentagonal pyramid, the trigonal prism and the octahedron. More often than not, however, real world structures deviate from those ideal geometries, and we try to cope with non-ideality by adding adjectives such as distorted, twisted, puckered or flattened, additionally nuanced by adverbs such as slightly, significantly or severely. This contribution presents a systematic structural perspective of six-atom groups in molecules by means of a continuous shape measures (CShM) analysis. The shape of a group of N points is defined by all the sets of 3 N Cartesian coordinates that can be generated by rigid translation, rotation, or isotropic scale change. Among all possible arrangements of N points in space, we select as reference shapes the corresponding regular N-vertex polygons and polyhedra, together with univocally defined combinations thereof (e.g., two coplanar or perpendicular edge-sharing squares). The present CShM study allows us to classify most of the structures not only by their closeness to a particular regular shape, but also by quantifying their position along minimal distortion interconversion pathways between two regular shapes.