Bismuth Coordination Polymers with Fluorinated Linkers: Aqueous Stability, Bivolatility, and Adsorptive Behavior.

Bismuth metal-organic frameworks and coordination polymers (CP) are challenging to synthesize, given the poor solubility of bismuth precursors and asymmetric and labile ligation of Bi3+ due to its intrinsic lone pair. Here, we synthesize and structurally characterize three Bi3+-CPs, exploiting a tetrafluoroterephtalate (F4BDC) linker to determine the effect of high acidity on these synthesis and coordination challenges. Single-crystal X-ray diffraction characterization showed that pi-pi stacking of linkers directs framework arrangement and generally deters open porosity in the three structures, respectively featuring Bi chains (Bi chain -F 4 BDC), Bi dimers (Bi 2 -F 4 BDC) linked into chains, and Bi tetramers (Bi 4 -F 4 BDC). Powder X-ray diffraction and microscopic imaging show the high purity and stability of these compounds in water. Naphthalenedisulfonate (NDS) was used as a mineralizer in the synthesis of (Bi chain -F 4 BDC) and (Bi 4 -F 4 BDC), and studies of its role in assembly pathways yielded two additional structures featuring mixed NDS and F4BDC, respectively, linking monomer and octamer Bi nodes, and confirmed that F4BDC is the preferred (less labile) linker. Methylene blue (MB) adsorption studies show differing efficacies of the three Bi-F4BDC phases, attributed to surface characteristics of the preferential growth facets, while generally most effective adsorption is attributed to the hydrophobicity of fluorinated ligands. Finally, thermogravimetric analysis of all three Bi-F4BDC phases indicates simultaneous ligand degradation and in situ formation of volatile Bi compounds, which could be exploited in the chemical vapor deposition of Bi-containing thin films.

Bismuth-Polyoxocation Coordination Networks: Controlling Nuclearity and Dimension-Dependent Photocatalysis.

Bismuth-oxocluster nodes for metal-organic frameworks (MOFs) and coordination networks/polymers are less prolific than other families featuring zinc, zirconium, titanium, lanthanides, etc. However, Bi3+ is non-toxic, it readily forms polyoxocations, and its oxides are exploited in photocatalysis. This family of compounds provides opportunity in medicinal and energy applications. Here, we show that Bi node nuclearity depends on solvent polarity, leading to a family of Bix-sulfonate/carboxylate coordination networks with x = 1-38. Larger nuclearity-node networks were obtained from polar and strongly coordinating solvents, and we attribute the solvent's ability to stabilize larger species in solution. The strong role of the solvent and the lesser role of the linker in defining node topologies differ from other MOF syntheses, and this is due to the Bi3+ intrinsic lone pair that leads to weak node-linker interactions. We describe this family by single-crystal X-ray diffraction (eleven structures), obtained in pure forms and high yields. Ditopic linkers include NDS (1,5-naphthalenedisulfonate), DDBS (2,2'-[biphenyl-4,4'-diylchethane-2,1-diyl] dibenzenesulphonate), and NH2-benzendicarboxylate (BDC). While the BDC and NDS linkers yield more open-framework topologies that resemble those obtained by carboxylate linkers, topologies with DDBS linkers appear to be in part driven by association between DDBS molecules. An in situ small-angle X-ray scattering study of Bi38-DDBS reveals stepwise formation, including Bi38-assembly, pre-organization in solution, followed by crystallization, confirming the less important role of the linker. We demonstrate photocatalytic hydrogen (H2) generation with select members of the synthesized materials without the benefit of a co-catalyst. Band gap determination from X-ray photoelectron spectroscopy (XPS) and UV-vis data suggest the DDBS linker effectively absorbs in the visible range with ligand-to-Bi-node charge transfer. In addition, materials containing more Bi (larger Bi38-nodes or Bi6 inorganic chains) exhibit strong UV absorption, also contributing to effective photocatalysis by a different mechanism. All tested materials became black with extensive UV-vis exposure, and XPS, transmission electron microscopy, and X-ray scattering of the black Bi38-framework suggest that Bi0 is formed in situ, without phase segregation. This evolution leads to enhanced photocatalytic performance, perhaps due to increased light absorption.

Investigation of the Solution Chemistry of Hybrid Organic-Inorganic Indium Halides for New Material Discovery.

Recently, metal halide perovskites (MHPs) have emerged as a new class of materials for optical and electronic applications such as solar cells and ionizing radiation detectors. Although the solution-processability of MHPs is among their greatest advantages, the solution chemistries of most metal halide systems and their relationship with the observed structural and chemical diversity are poorly understood. In this work, we study the solution chemistry of a model indium halide system, methylammonium (MA)-In-Br, using a combination of the UV-vis spectroscopy, electrospray ionization mass spectrometry (ESI-MS) measurements, small-angle X-ray scattering (SAXS), and density functional theory (DFT) calculations. Our results show that indium could form either octahedral [InBr63-] or tetrahedral [InBr4-] anions in solution or a combination of both, depending on the loading ratios of MABr and InBr3 reactants. Understanding the solution chemistry of this system and recognizing the optical fingerprints of these polyanions allow for targeted crystallization of two novel compounds: MAInBr4 featuring tetrahedral [InBr4-] anions and MA2InBr5 containing both octahedral [InBr63-] and tetrahedral [InBr4-] anions. Further increase of the MABr content leads to the formation of previously reported MA4InBr7, containing only octahedral [InBr63-] anions separated by Br- anions. Our results suggest that understanding the solution chemistry of multinary metal halide systems could be a valuable tool for discovering functional materials for practical applications.

Oxo-Cluster-Based Zr/HfIV Separation: Shedding Light on a 70-Year-Old Process.

Zirconium and hafnium in the tetravalent oxidation state are considered the two most similar elements on the periodic table, based on their coexistence in nature and their identical solid-state chemistry. However, differentiating solution phase chemistry is crucial for their separation for nuclear applications that exploit the neutron capture of Hf and neutron transparency of Zr. Here we provide molecular level detail of the multiple factors that influence Zr/Hf separation in a long-exploited, empirically designed industrial solvent-extraction process that favors Hf extraction into an organic phase. In the aqueous solution, both Hf and Zr form an oxo-centered tetramer cluster with a core formula of [OM4(OH)6(NCS)12]4- (OM4-NCS, M = Hf, Zr). This was identified by single-crystal X-ray diffraction, as well as small-angle X-ray scattering (SAXS), of both the aqueous and organic phase. In addition to this phase, Zr also forms (1) a large oxo-cluster formulated [Zr48O30(OH)92(NCS)40(H2O)40] (Zr48) and (2) NCS adducts of OZr4-NCS. Zr48 was identified first by SAXS and then crystallized by exploiting favorable soft-metal bonding to the sulfur of NCS. While the large Zr48 likely cannot be extracted due to its larger size, the NCS adducts of OZr4-NCS are also less favorable to extraction due to the extra negative charge, which necessitates coextraction of an additional countercation (NH4+) per extra NCS ligand. Differentiating Zr and Hf coordination and hydrolysis chemistry adds to our growing understanding that these two elements, beyond simple solid-state chemistry, have notable differences in chemical reactivity.

Solvent-Driven Transformation of Zn/Cd2+-Deoxycholate Assemblies.

Deoxycholic acid (DOC) is a unique, biologically derived surfactant with facial amphiphilicity that has been exploited, albeit minimally, in supramolecular assembly of materials. Here, we present the synthesis and structural characterization of three hybrid metal (Zn2+ and Cd2+)-DOC compounds. Analysis by single-crystal X-ray diffraction reveals the many interactions that are possible between these facial surfactants and the influence of solvent molecules that drive the assembly of materials. These structures are the first metal-DOC complexes besides those obtained from alkali and alkaline earth metals. We isolated polymeric chains of both Cd and Zn (Znpoly-DOC and Cdpoly-DOC) from water. Major interactions between DOC molecules in these phases are hydrophobic in nature. Cdpoly-DOC exhibits unique P1 symmetry, with complete interdigitation of the amphiphiles between neighboring polymeric chains. Zn4-DOC, obtained from methanol dissolution of Znpoly-DOC, features the OZn4 tetrahedron, widely known in basic zinc acetate and MOF-5 (metal organic framework). We document a solvent-driven, room-temperature transition between Znpoly-DOC and Zn4-DOC (in both directions) by scanning and transmission electron microscopies in addition to small-angle X-ray scattering, powder X-ray diffraction, and infrared spectroscopy. These studies show the methanol-driven transition of Znpoly-DOC to Zn4-DOC occurs via an intermediate with no long-range order of the Zn4 clusters, indicating the strongest interactions driving assembly are intramolecular. On the contrary, water-driven solid-to-solid transformation from Zn4-DOC to Znpoly-DOC exhibits crystal-to-crystal transformation. Znpoly-DOC is robust, easy to synthesize, and comprised of biologically benign components, so we demonstrate dye absorption as a proxy for water treatment applications. It favors absorption of positively charged dyes. These studies advance molecular level knowledge of the supramolecular assembly of facial surfactants that can be exploited in the design of organic-inorganic hybrid materials. This work also highlights the potential of solvent for tuning supramolecular assembly processes, leading to new hybrid materials featuring facial surfactants.

Unraveling Nanoscale Cobalt Oxide Catalysts for the Oxygen Evolution Reaction: Maximum Performance, Minimum Effort.

The oxygen evolution reaction (OER) is a key bottleneck step of artificial photosynthesis and an essential topic in renewable energy research. Therefore, stable, efficient, and economical water oxidation catalysts (WOCs) are in high demand and cobalt-based nanomaterials are promising targets. Herein, we tackle two key open questions after decades of research into cobalt-assisted visible-light-driven water oxidation: What makes simple cobalt-based precipitates so highly active-and to what extent do we need Co-WOC design? Hence, we started from Co(NO3)2 to generate a precursor precipitate, which transforms into a highly active WOC during the photocatalytic process with a [Ru(bpy)3]2+/S2O82-/borate buffer standard assay that outperforms state of the art cobalt catalysts. The structural transformations of these nanosized Co catalysts were monitored with a wide range of characterization techniques. The results reveal that the precipitated catalyst does not fully change into an amorphous CoOx material but develops some crystalline features. The transition from the precipitate into a disordered Co3O4 material proceeds within ca. 1 min, followed by further transformation into highly active disordered CoOOH within the first 10 min. Furthermore, under noncatalytic conditions, the precursor directly transforms into CoOOH. Moreover, fast precipitation and isolation afford a highly active precatalyst with an exceptional O2 yield of 91% for water oxidation with the visible-light-driven [Ru(bpy)3]2+/S2O82- assay, which outperforms a wide range of carefully designed Co-containing WOCs. We thus demonstrate that high-performance cobalt-based OER catalysts indeed emerge effortlessly from a self-optimization process favoring the formation of Co(III) centers in all-octahedral environments. This paves the way to new low-maintenance flow chemistry OER processes.

Deliberate Construction of Polyoxoniobates Exploiting the Carbonate Ligand.

Polyoxometalates (POMs, metals=VV , NbV , TaV , MoVI , WVI ) are molecular metal oxides that can be isolated without capping ligands. The high negative charge of polyoxoniobates (PONb) provides strong interactions with heterocations, advantageous for electrostatic assembly of modular materials. In four single-crystal X-ray structures, we demonstrate that carbonate combined with the very reactive decaniobate [Nb10 O28 ]6- reassembles into a new decaniobate, [Nb10 O25 (CO3 )6 ]12- , featuring three carbonate-ligated Nb-polyhedra. These Nb-sites can be replaced by heterometals (lanthanides), and the tridentate carbonate can serve as an anchor point to build niobate-frameworks. Small-angle X-ray scattering and two additional X-ray structures reveal that the reaction pathway proceeds through a Nb24 -PONb intermediate, and the obtained PONb (with or without carbonate) is counterion, temperature, and solvent-dependent (water or mixed water-methanol). This provides an uncommon level of control for PONb chemistry.

Electro-Optical Properties of Monolayer and Bilayer Pentagonal BN: First Principles Study.

Two-dimensional hexagonal boron nitride (hBN) is an insulator with polar covalent B-N bonds. Monolayer and bilayer pentagonal BN emerge as an optoelectronic material, which can be used in photo-based devices such as photodetectors and photocatalysis. Herein, we implement spin polarized electron density calculations to extract electronic/optical properties of mono- and bilayer pentagonal BN structures, labeled as B 2 N 4 , B 3 N 3 , and B 4 N 2 . Unlike the insulating hBN, the pentagonal BN exhibits metallic or semiconducting behavior, depending on the detailed pentagonal structures. The origin of the metallicity is attributed to the delocalized boron (B) 2p electrons, which has been verified by electron localized function and electronic band structure as well as density of states. Interestingly, all 3D networks of different bilayer pentagonal BN are dynamically stable unlike 2D structures, whose monolayer B 4 N 2 is unstable. These 3D materials retain their metallic and semiconductor nature. Our findings of the optical properties indicate that pentagonal BN has a visible absorption peak that is suitable for photovoltaic application. Metallic behavior of pentagonal BN has a particular potential for thin-film based devices and nanomaterial engineering.

Discrete Hf18 Metal-oxo Cluster as a Heterogeneous Nanozyme for Site-Specific Proteolysis.

The selective hydrolysis of proteins by non-enzymatic catalysis is difficult to achieve, yet it is crucial for applications in biotechnology and proteomics. Herein, we report that discrete hafnium metal-oxo cluster [Hf18 O10 (OH)26 (SO4 )13 ⋅(H2 O)33 ] (Hf18 ), which is centred by the same hexamer motif found in many MOFs, acts as a heterogeneous catalyst for the efficient hydrolysis of horse heart myoglobin (HHM) in low buffer concentrations. Among 154 amino acids present in the sequence of HHM, strictly selective cleavage at only 6 solvent accessible aspartate residues was observed. Mechanistic experiments suggest that the hydrolytic activity is likely derived from the actuation of HfIV Lewis acidic sites and the Brønsted acidic surface of Hf18 . X-ray scattering and ESI-MS revealed that Hf18 is completely insoluble in these conditions, confirming the HHM hydrolysis is caused by a heterogeneous reaction of the solid Hf18 cluster, and not from smaller, soluble Hf species that could leach into solution.

Bismuth for Controlled Assembly/Disassembly of Transition-Metal Oxo Clusters, Defining Reaction Pathways in Inorganic Synthesis and Nature.

Trivalent bismuth is a unique heavy p-block ion. It is highly insoluble in water, due to strong hydrolysis tendencies, and known for low toxicity. Its lone pair is structure-directing, providing framework materials with structural flexibility, leading to piezoelectric and multiferroic function. The flexibility it provides is also advantageous for dopants and vacancies, giving rise to conductivity, luminescence, color, and catalytic properties. We are exploiting Bi3+ in a completely different way, as a knob to "tune" the solubility and stability of transition-metal oxo clusters. The lone pair allows capping and isolation of metastable cluster forms for solid-state and solution characterization. With controlled release of the bismuth (via bismuth oxyhalide metathesis), the metal oxo clusters can be retained in aqueous solution, and we can track their reaction pathways and conversion to related metal oxyhydroxides. Here we present isolation of a bismuth-stabilized MnIV cluster, fully formulated [MnIV6Bi2KO9(CH3COO)10(H2O)3(NO3)2] (Mn6Bi2). In addition to characterization by single-crystal X-ray diffraction, solution characterization in acetonitrile and acetonitrile-acetic acid by small-angle X-ray scattering (SAXS) and electrospray ionization mass spectrometry shows high stability and the tendency of Mn6Bi2 to link into chains by bridging the bismuth (and potassium) caps with nitrate and acetate ligands. On the other hand, the dissolution of Mn6Bi2 in water, with and without metathesis of the bismuth, leads to the precipitation of related oxyhydroxide phases, which we characterized by transmission electron microscopy (TEM), electron diffraction, and energy-dispersive spectroscopy, and the conversion pathway by SAXS. Without removal of bismuth, amorphous manganese/bismuth oxyhydroxides precipitate within a day. On the other hand, metathesis of BiOBr yields a solution containing soluble manganese oxyhydroxide prenucleation clusters that assemble and precipitate over 10 days. This allows tracking of the reaction pathway via SAXS. We observe one-dimensional growth of species, followed by the precipitation of nanocrystalline hollandite (identified by TEM). The hollandite is presumably templated by the K+, originally in the crystalline lattice of Mn6Bi2. In this Forum Article that combines new results and prospective, we compare these results to prior studies in which we first introduced the use of capping Bi3+ to stabilize reactive clusters, followed by destabilization to understand reaction pathways in synthesis and low-temperature geochemistry.

Atomically Precise Lanthanide-Iron-Oxo Clusters Featuring the ϵ-Keggin Ion.

Atomically precise molecular metal-oxo clusters provide ideal models to understand metal oxide surfaces, self-assembly, and form-function relationships. Devising strategies for synthesis and isolation of these molecular forms remains a challenge. Here, the synthesis of four Ln-Fe oxo clusters that feature the ϵ-{Fe13 } Keggin cluster in their core is reported. The {Fe13 } metal-oxo cluster motif is the building block of two important iron oxyhydroxyide phases in nature and technology, ferrihydrite (as the δ-isomer) and magnetite (the ϵ-isomer). The reported ϵ-{Fe13 } Keggin isomer as an isolated molecule provides the opportunity to study the formation of ferrihydrite and magnetite from this building unit. The four currently reported isostructural lanthanide-iron-oxo clusters are fully formulated [Y12 Fe33 (TEOA)12 (Hyp)6 (µ3 -OH)20 (µ4 -O)28 (H2 O)12 ](ClO4 )23 ⋅50 H2 O (1, Y12 Fe33 ), [Gd12 Fe33 (TEOA)12 (Hyp)6 (µ3 -OH)20 (µ4 -O)32 (H2 O)12 ](ClO4 )15 ⋅50 H2 O (2, Gd12 Fe33 ) and [Ln16 Fe29 (TEOA)12 (Hyp)6 (µ3 -OH)24 (µ4 -O)28 (H2 O)16 ](ClO4 )16 (NO3 )3 ⋅n H2 O (Ln=Y for 3, Y16 Fe29 , n=37 and Ln=Gd for 4, Gd16 Fe29 n=25; Hyp=trans-4-Hydroxyl-l-proline and TEOA=triethanolamine). The next metal layer surrounding the ϵ-{Fe13 } core within these clusters exhibits a similar arrangement as the magnetite lattice, and Fe and Ln can occupy the same positions. This provides the opportunity to construct a family of compounds and optimize magnetic exchange in these molecules through composition tuning. Small-angle X-ray scattering (SAXS) and high-resolution electrospray ionization mass spectrometry (HRESI-MS) show that these clusters are stable upon dissolution in both water and organic solvents, as a first step to performing further chemistry towards building magnetic arrays or investigating ferrihydrite and magnetite assembly from pre-nucleation clusters.

Stabilizing Reactive Fe(III) Clusters by Freeze-Dry/Solvent-Exchange To Benchmark Iron Hydrolysis Pathways.

Isolating Fe(III) clusters from water without stabilizing ligands is significantly challenged by the high acidity of Fe3+-bound water, leading to uncontrolled precipitation of iron oxyhydroxides. Here we demonstrate a freeze-drying solvent-exchange method that enabled the isolation of a metastable Fe(III) sulfate decameric cluster formulated [Fe10O2(SO4)12(OCH3)2]·14CH3OH (Fe10). Without stabilization by solvent-exchange, the aqueous species undergoes rapid conversion to the iron sulfate mineral schwertmannite. Monitoring the hydrolysis process from cluster intermediates to schertmannite by small-angle X-ray scattering, we observe the progression from Fe10 to 37 Å soluble nanoparticles prior to the precipitation process. This condensation behavior of Fe10 is further exploited to develop a simple laboratory synthesis of schwetmannite. In addition, we demonstrate the versatility of the freeze-drying solvent-exchange method by isolating Al(III), Zn(II), and Cd(II) substituted Fe(III) sulfate clusters. The freeze-drying solvent-exchange method provides a unique opportunity to isolate cluster intermediates and models to aid in our understanding of metal-ion hydrolysis processes in environmental, material science, and geological studies.

The Role of Bi3+ in Promoting and Stabilizing Iron Oxo Clusters in Strong Acid.

Metal oxo clusters and metal oxides assemble and precipitate from water in processes that depend on pH, temperature, and concentration. Other parameters that influence the structure, composition, and nuclearity of "molecular" and bulk metal oxides are poorly understood, and have thus not been exploited. Herein, we show that Bi3+ drives the formation of aqueous Fe3+ clusters, usurping the role of pH. We isolated and structurally characterized a Bi/Fe cluster, Fe3 BiO2 (CCl3 COO)8 (THF)(H2 O)2 , and demonstrated its conversion into an iron Keggin ion capped by six Bi3+ irons (Bi6 Fe13 ). The reaction pathway was documented by X-ray scattering and mass spectrometry. Opposing the expected trend, increased cluster nuclearity required a pH decrease instead of a pH increase. We attribute this anomalous behavior of Bi/Fe(aq) solutions to Bi3+ , which drives hydrolysis and condensation. Likewise, Bi3+ stabilizes metal oxo clusters and metal oxides in strongly acidic conditions, which is important in applications such as water oxidation for energy storage.

Pattern extraction for high-risk accidents in the construction industry: a data-mining approach.

Accidents involving falls and falling objects (group I) are highly frequent accidents in the construction industry. While being hit by a vehicle, electric shock, collapse in the excavation and fire or explosion accidents (group II) are much less frequent, they make up a considerable proportion of severe accidents. In this study, multiple-correspondence analysis, decision tree, ensembles of decision tree and association rules methods are employed to analyse a database of construction accidents throughout Iran between 2007 and 2011. The findings indicate that in group I, there is a significant correspondence among these variables: time of accident, place of accident, body part affected, final consequence of accident and lost workdays. Moreover, the frequency of accidents in the night shift is less than others, and the frequency of injury to the head, back, spine and limbs are more. In group II, the variables time of accident and body part affected are mostly related and the frequency of accidents among married and older workers is more than single and young workers. There was a higher frequency in the evening, night shifts and weekends. The results of this study are totally in line with the previous research.

Risk-based Analysis of Construction Accidents in Iran During 2007-2011-Meta Analyze Study.

BACKGROUND: The present study aimed to investigate the characteristics of occupational accidents and frequency and severity of work related accidents in the construction industry among Iranian insured workers during the years 20072011. METHODS: The Iranian Social Security Organization (ISSO) accident database containing 21,864 cases between the years 2007-2011 was applied in this study. In the next step, Total Accident Rate (TRA), Total Severity Index (TSI), and Risk Factor (RF) were defined. The core of this work is devoted to analyzing the data from different perspectives such as age of workers, occupation and construction phase, day of the week, time of the day, seasonal analysis, regional considerations, type of accident, and body parts affected. RESULTS: Workers between 15-19 years old (TAR=13.4%) are almost six times more exposed to risk of accident than the average of all ages (TAR=2.51%). Laborers and structural workers (TAR=66.6%) and those working at heights (TAR=47.2%) experience more accidents than other groups of workers. Moreover, older workers over 65 years old (TSI=1.97%> average TSI=1.60%), work supervisors (TSI=12.20% >average TSI=9.09%), and night shift workers (TSI=1.89% >average TSI=1.47%) are more prone to severe accidents. CONCLUSION: It is recommended that laborers, young workers, weekend and night shift workers be supervised more carefully in the workplace. Use of Personal Protective Equipment (PPE) should be compulsory in working environments, and special attention should be undertaken to people working outdoors and at heights. It is also suggested that policymakers pay more attention to the improvement of safety conditions in deprived and cold western regions.