New insight into identifying sediment phosphorus sources in multi-source polluted urban river: Effect of environmental-induced microbial community succession on stability of microbial source tracking results.

Identifying sediment phosphorus sources, the key to control eutrophication, is hindered in multi-source polluted urban rivers by the lack of appropriate methods and data resolution. Community-based microbial source tracking (MST) offers new insight, but the bacterial communities could be affected by environmental fluctuations during the migration with sediments, which might induce instability of MST results. Therefore, the effects of environmental-induced community succession on the stability of MST were compared in this study. Liangxi River, a highly eutrophic urban river, was selected as the study area where sediment phosphorus sources are difficult to track because of multi-source pollution and complicated hydrodynamic conditions. Spearman correlation analysis (P < 0.05) was conducted to recognize a close relationship between sediment, bacterial communities and phosphorus, verifying the feasibility of MST for identify sediment phosphorus sources. Two distinct microbial community fingerprints were constructed based on whether excluded 113 vulnerable species, which were identified by analyzing the differences of microorganisms across a concentration gradient of exogenous phosphorus input in microbial environmental response experiment. Because of the lower unknown proportion and relative standard deviations, MST results were more stable and reliable when based on the fingerprints excluding species vulnerable to phosphorus. This study presents a novel insight on how to identify sediment phosphorus sources in multi-source polluted urban river, and would help to develop preferential control strategies for eutrophication management.

Conceptual and Practical Aspects of Metal-Organic Frameworks for Solid-Gas Reactions.

The presence of site-isolated and well-defined metal sites has enabled the use of metal-organic frameworks (MOFs) as catalysts that can be rationally modulated. Because MOFs can be addressed and manipulated through molecular synthetic pathways, they are chemically similar to molecular catalysts. They are, nevertheless, solid-state materials and therefore can be thought of as privileged solid molecular catalysts that excel in applications involving gas-phase reactions. This contrasts with homogeneous catalysts, which are overwhelmingly used in the solution phase. Herein, we review theories dictating gas phase reactivity within porous solids and discuss key catalytic gas-solid reactions. We further treat theoretical aspects of diffusion within confined pores, the enrichment of adsorbates, the types of solvation spheres that a MOF might impart on adsorbates, definitions of acidity/basicity in the absence of solvent, the stabilization of reactive intermediates, and the generation and characterization of defect sites. The key catalytic reactions we discuss broadly include reductive reactions (olefin hydrogenation, semihydrogenation, and selective catalytic reduction), oxidative reactions (oxygenation of hydrocarbons, oxidative dehydrogenation, and carbon monoxide oxidation), and C-C bond forming reactions (olefin dimerization/polymerization, isomerization, and carbonylation reactions).

Room-Temperature Quantitative Quantum Sensing of Lithium Ions with a Radical-Embedded Metal-Organic Framework.

Recent advancements in quantum sensing have sparked transformative detection technologies with high sensitivity, precision, and spatial resolution. Owing to their atomic-level tunability, molecular qubits and ensembles thereof are promising candidates for sensing chemical analytes. Here, we show quantum sensing of lithium ions in solution at room temperature with an ensemble of organic radicals integrated in a microporous metal-organic framework (MOF). The organic radicals exhibit electron spin coherence and microwave addressability at room temperature, thus behaving as qubits. The high surface area of the MOF promotes accessibility of the guest analytes to the organic qubits, enabling unambiguous identification of lithium ions and quantitative measurement of their concentration through relaxometric and hyperfine spectroscopic methods based on electron paramagnetic resonance (EPR) spectroscopy. The sensing principle presented in this work is applicable to other metal ions with nonzero nuclear spin.

How Reproducible are Surface Areas Calculated from the BET Equation?

Porosity and surface area analysis play a prominent role in modern materials science. At the heart of this sits the Brunauer-Emmett-Teller (BET) theory, which has been a remarkably successful contribution to the field of materials science. The BET method was developed in the 1930s for open surfaces but is now the most widely used metric for the estimation of surface areas of micro- and mesoporous materials. Despite its widespread use, the calculation of BET surface areas causes a spread in reported areas, resulting in reproducibility problems in both academia and industry. To prove this, for this analysis, 18 already-measured raw adsorption isotherms were provided to sixty-one labs, who were asked to calculate the corresponding BET areas. This round-robin exercise resulted in a wide range of values. Here, the reproducibility of BET area determination from identical isotherms is demonstrated to be a largely ignored issue, raising critical concerns over the reliability of reported BET areas. To solve this major issue, a new computational approach to accurately and systematically determine the BET area of nanoporous materials is developed. The software, called "BET surface identification" (BETSI), expands on the well-known Rouquerol criteria and makes an unambiguous BET area assignment possible.

Dimensionality Modulates Electrical Conductivity in Compositionally Constant One-, Two-, and Three-Dimensional Frameworks.

We reveal here the construction of Ni-based metal-organic frameworks (MOFs) and conjugated coordination polymers (CCPs) with different structural dimensionalities, including closely π-stacked 1D chains (Ni-1D), aggregated 2D layers (Ni-2D), and a 3D framework (Ni-3D), based on 2,3,5,6-tetraamino-1,4-hydroquinone (TAHQ) and its various oxidized forms. These materials have the same metal-ligand composition but exhibit distinct electronic properties caused by different dimensionalities and supramolecular interactions between SBUs, ligands, and structural motifs. The electrical conductivity of these materials spans nearly 8 orders of magnitude, approaching 0.3 S/cm.

New insights into identifying sediment phosphorus sources in river-lake coupled system: A framework for optimizing microbial community fingerprints.

Identifying sediment phosphorus sources in river-lake coupled system is a question in developing preferential control strategies for phosphorus. As sediments adsorbed phosphorus and microbes would be transported with changing hydrodynamic, the phosphorus source-specific microbial community fingerprints shed light on determining the major sediment phosphorus sources. However, the identification of microbial community fingerprints is a challenge because both microbial succession and hydrological characteristics of river-lake systems would affect the stability of fingerprints. Therefore, this study provided a framework for optimizing phosphorus source-specific microbial community fingerprints, and attempted to identify the major sources of sediment phosphorus in river-lake coupled ecosystem. Meiliang Lake is one of the highly eutrophic area in Taihu Lake, where the sediments, bacterial communities, and phosphorus had a close relationship. Through analyzing the connectivity of microbes along water continuum, a microbial fingerprints candidate database was constructed. The phosphorus-related bacterial communities were screened and optimized by comparing the difference of predicted results between upstream and downstream, forming the stable microbial community fingerprints which consisted of Bacteroidia, Bacilli, Clostridia, and other species at the class level. SourceTracker results that based on the optimized phosphorus source-specific microbial community fingerprints indicated that the major sediment phosphorus sources to Meiliang Lake were Liangxi River, Wujingang River, and Donghuandi River, with the relative standard deviations ranging from 2.59% to 27.56%. The accuracy of phosphorus source apportionments was further confirmed based on the composite pollution index and hydrodynamic condition. This study put forward suggestions on how to improve the stability of microbial community fingerprints, and would help to improve the understanding of applying microbial source tracking method to identify the sources of abiotic pollution like sediment phosphorus.

Isolation of a Side-On V(III)-(η2-O2) through the Intermediacy of a Low-Valent V(II) in a Metal-Organic Framework.

We report the isolation of vanadium(II) in a metal-organic framework (MOF) by the reaction of the chloride-capped secondary building unit in the all-vanadium(III) V-MIL-101 (1) with 1,4-bis(trimethylsilyl)-2,3,5,6-tetramethyl-1,4-dihydropyrazine. The reduced material, 2, has a secondary building unit with the formal composition [VIIV2III], with each metal ion presenting one open coordination site. Subsequent reaction with O2 yields a side-on η2 vanadium-superoxo species, 3. The MOF featuring V(III)-superoxo moieties exhibits a mild enhancement in the isosteric enthalpy of adsorption for methane compared to the parent V-MIL-101. We present this synthetic methodology as a potentially broad way to access low-valent open metal sites within MOFs without causing a loss of crystallinity or porosity. The low-valent sites can serve as isolable intermediates to access species otherwise inaccessible by direct synthesis.

Spectroscopic Evidence of Hyponitrite Radical Intermediate in NO Disproportionation at a MOF-Supported Mononuclear Copper Site.

Dianionic hyponitrite (N2 O22- ) is often proposed, based on model complexes, as the key intermediate in reductive coupling of nitric oxide to nitrous oxide at the bimetallic active sites of heme-copper oxidases and nitric oxide reductases. In this work, we examine the gas-solid reaction of nitric oxide with the metal-organic framework CuI -ZrTpmC* with a suite of in situ spectroscopies and density functional theory simulations, and identify an unusual chelating N2 O2.- intermediate. These results highlight the advantage provided by site-isolation in metal-organic frameworks (MOFs) for studying important reaction intermediates, and provide a mechanistic scenario compatible with the proposed one-electron couple in these enzymes.

Thermal Cycling of a MOF-Based NO Disproportionation Catalyst.

The metal-organic framework CuI-MFU-4l reacts with NO, initially forming a copper(I)-nitrosyl at low pressure, and subsequently generates NO disproportionation products CuII-NO2 and N2O. The thermal stability of MFU-4l allows NOx to be released from the framework at temperatures greater than 200 °C. This treatment regenerates the original CuI-MFU-4l, which can engage in subsequent cycles of NO disproportionation.

Atomically precise single-crystal structures of electrically conducting 2D metal-organic frameworks.

Electrically conducting 2D metal-organic frameworks (MOFs) have attracted considerable interest, as their hexagonal 2D lattices mimic graphite and other 2D van der Waals stacked materials. However, understanding their intrinsic properties remains a challenge because their crystals are too small or of too poor quality for crystal structure determination. Here, we report atomically precise structures of a family of 2D π-conjugated MOFs derived from large single crystals of sizes up to 200 µm, allowing atomic-resolution analysis by a battery of high-resolution diffraction techniques. A designed ligand core rebalances the in-plane and out-of-plane interactions that define anisotropic crystal growth. We report two crystal structure types exhibiting analogous 2D honeycomb-like sheets but distinct packing modes and pore contents. Single-crystal electrical transport measurements distinctively demonstrate anisotropic transport normal and parallel to the π-conjugated sheets, revealing a clear correlation between absolute conductivity and the nature of the metal cation and 2D sheet packing motif.

Continuous Electrical Conductivity Variation in M3(Hexaiminotriphenylene)2 (M = Co, Ni, Cu) MOF Alloys.

We report on the continuous fine-scale tuning of band gaps over 0.4 eV and of the electrical conductivity of over 4 orders of magnitude in a series of highly crystalline binary alloys of two-dimensional electrically conducting metal-organic frameworks M3(HITP)2 (M = Co, Ni, Cu; HITP = 2,3,6,7,10,11-hexaiminotriphenylene). The isostructurality in the M3(HITP)2 series permits the direct synthesis of binary alloys (MxM'3-x)(HITP)2 (MM' = CuNi, CoNi, and CoCu) with metal compositions precisely controlled by precursor ratios. We attribute the continuous tuning of both band gaps and electrical conductivity to changes in free-carrier concentrations and to subtle differences in the interlayer displacement or spacing, both of which are defined by metal substitution. The activation energy of (CoxNi3-x)(HITP)2 alloys scales inversely with an increasing Ni percentage, confirming thermally activated bulk transport.

Identifying key environmental factors for enhancing the pollutant removal potential at a river confluence.

The confluence area of river networks is a hot spot for pollutant removal. As an essential part of the river ecosystem, sediment bacterial communities played a crucial role in the removal of pollutants. However, how the potential of sediment bacterial communities can be enhanced toward the removal of pollutants remains unclear. Therefore, this study provides a new approach for the identification of key environmental factors that enhance the pollutant removal potential at a river confluence, integrating the bacteria-based index of biotic integrity (Ba-IBI), path model, support vector regression (SVR) model, and sensitivity analysis. The developed Ba-IBI could quantitatively evaluate the differences of both structure and function of bacterial communities before and after the confluence, with a range from 1.52 to 2.78. The flow regime, which was represented by the Froude number, exerted an indirect effect on Ba-IBI mediated through water nutrients and sediment nutrients according to path model results. Sediment nutrients and water nutrients were considered as the main environmental factors that directly affected sediment bacterial communities. A function that could predict the response of sediment bacterial communities to environmental factors in the best possible way was found through SVR modeling, with R2 = 0.8357. The results of the sensitivity analysis indicated that the total phosphorus in water and ammonia nitrogen in sediments were key environmental factors for enhancing the pollutant removal potential at the river confluence. The established approach aids the improvement of the bioremediation potential of river confluence area, and might provide a theoretical basis for watershed restoration.

Reversible Metalation and Catalysis with a Scorpionate-like Metallo-ligand in a Metal-Organic Framework.

The installation of metallo-ligands in metal-organic frameworks (MOFs) is an effective means to create site-isolated metal centers toward single-site heterogeneous catalysis. Although trispyrazolyborate (Tp) and tripyrazolylmethane (Tpm) form one of the most iconic classes of homogeneous catalysts, neither has been used as a metallo-ligand for the generation of MOFs thus far. Here, we show that upon in situ metalation with CuI, a tricarboxylated Tpm ligand reacts with ZrOCl2 to generate a new MOF exhibiting neutral scorpionate-like chelating sites. These sites undergo for facile demetalation and remetalation with retention of crystallinity and porosity. When remetalated with CuI, the MOF exhibits spectroscopic features and catalytic activity for olefin cyclopropanation reactions that are similar to the molecular [Cu(CH3CN)Tpm*]PF6 complex (Tpm* = tris(3,5-dimethylpyrazolyl)methane). These results demonstrate the inclusion of Tp or Tpm metallo-ligands in a MOF for the first time and provide a blueprint for immobilizing Tpm* catalysts in a spatially isolated and well-defined environment.

Luminescent Tungsten(VI) Complexes: Photophysics and Applicability to Organic Light-Emitting Diodes and Photocatalysis.

The synthesis, excited-state dynamics, and applications of two series of air-stable luminescent tungsten(VI) complexes are described. These tungsten(VI) complexes show phosphorescence in the solid state and in solutions with emission quantum yields up to 22 % in thin film (5 % in mCP) at room temperature. Complex 2 c, containing a 5,7-diphenyl-8-hydroxyquinolinate ligand, displays prompt fluorescence (blue-green) and phosphorescence (red) of comparable intensity, which could be used for ratiometric luminescent sensing. Solution-processed organic light-emitting diodes (OLEDs) based on 1 d showed a stable yellow emission with an external quantum efficiency (EQE) and luminance up to 4.79 % and 1400 cd m-2 respectively. These tungsten(VI) complexes were also applied in light-induced aerobic oxidation reactions.