Solid-state Magic Angle Spinning Research Articles

Unveiling the structure of calcium borate glass by neutron diffraction, MAS-NMR, Raman and first-principles calculations

Calcium borate glass is a challenging system, due to the rich variety of borate units and alterable boron coordination number, and hence they are also of particular interest for academic study. In this study, neutron diffraction, solid-state magic angle spinning nuclear magnetic resonance (MAS-NMR) and Raman spectroscopy were combined with first-principles calculations, experience potential structure refinement (EPSR) simulations to investigate the structure of xCaO·(1-x)11B2O3 glass. Property data such as density and glass transition temperature were also measured to study the impact of structural changes on the properties of glasses. The structure of calcium borate glass was analyzed using various methods including structural unit, atomic pair bond length, coordination number, ring structure, chain structure and cavity distribution. Most notably, the atomic labeling method plays a key role in the structural analysis process. Through this method some new conclusions were obtained. For example, the increase of CaO content mainly leads to the conversion of BO to NBO in the glass structure, and has little effect on the content of BO3 and BØ4-. This result further leads to an increase in Ca-NBO interactions. Interestingly, the bond length distribution of Ca-NBO and B-NBO is shorter than that of Ca-BO and B-BO, so the glass structure becomes denser. The structural reason why the density of calcium borate glass is less than the crystal density was also revealed. This study contributes to unveiling the structure of calcium borate glass and exploring the correlation between the structure and properties of calcium borate glass, which provides a valuable reference for developing more valuable amorphous materials.

Surface Passivation by Embedment of Polyphosphate Inhibits the Aragonite-to-Calcite Thermodynamic Pump.

We monitored the conversion of aragonite to calcite in water by comparing single and mixed polymorph suspensions. We demonstrate that the enhanced aragonite-to-calcite conversion in mixed polymorph suspensions is dramatically inhibited by adding polyphosphate (sodium hexametaphosphate). 13C and 31P solid-state magic angle spinning (MAS) NMR and attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectra allow us to follow quantitatively these effects as imparted by the dissolution-recrystallization processes. 31P{13C} and 13C{31P} rotational echo double resonance (REDOR)NMR experiments reveal coprecipitated phosphate that is embedded only within the surfaces of both polymorphs during the initial dissolution and recrystallization processes, causing passivation that arrests phase conversion.

Effect of borate, fluoride and strontium ions on biomimetic nucleation of calcium phosphate studied using solid-state nuclear magnetic resonance and X-ray diffraction

ObjectivesApatite minerals can have various anions and cations in their crystal structure in addition to phosphate ion (PO₄³⁻) and calcium ion (Ca2+). The aim of this study is to investigate effects of the borate, fluoride and strontium ions on biomimetic nucleation of calcium phosphate. MethodsNano-crystalline hydroxyapatite (H-Ap) was obtained from a supersaturated buffered solution containing 4.12 mM HPO42- and 5.88 mM Ca2+ (H-Ap). Four additives were used in solid solution methods: (i) 0.588 mM F- (F-Ap), (ii) 5.88 mM Sr2+ (Sr-Ap), (iii) 4.12 mM BO33- (BO3-Ap), and (iv) a surface pre-reacted glass ionomer (S-PRG) filler eluate that contained 0.17 mM Sr2+, 0.588 mM F-, 11.1 mM BO33-- (SPRG-Ap). Apatite crystallization was investigated using a solid-state magic-angle spinning NMR spectroscopy and X-ray diffraction (XRD) with the Rietveld analysis. ResultsA 2D 1H–31P heteronuclear-correlation NMR showed F- ion incorporation in the apatite structure of the F-Ap and SPRG-Ap. The peaks on the 31P axis of the F-Ap, Sr-Ap, and BO3-Ap were different from that of the H-Ap, and the full width at half maximum increased in the following order: H-Ap∼F-Ap∼BO3-Ap< SPRG-Ap< Sr-Ap, suggesting the incorporation of the F-, Sr2+ and BO33-. The incorporation of F and BO3 was further confirmed by 19F and 11B NMR. The XRD revealed that Sr2+ was preferentially incorporated into the CaII site. SignificanceThe F-, Sr2+ and BO33-ions might be involved in modifying the crystallization of apatite precipitation, producing a variety of apatite. S-PRG filler that release these ions may have an effect on remineralization, i.e., the reformation of apatite lost due to caries.

Polarization Amplification in Dynamic Nuclear Polarization Magic-Angle Spinning Solid-State Nuclear Magnetic Resonance by Solubilizing Traditional Ionic Salts.

Dynamic nuclear polarization can improve the sensitivity of magic-angle spinning solid-state NMR experiments by 1-2 orders of magnitude. In aqueous media, experiments are usually performed using the so-called DNP juice, a glycerol-d8/D2O/H2O mixture (60/30/10, v/v/v) that can form a homogeneous glass at cryogenic temperatures. This acts as a cryoprotectant and prevents phase separation of the paramagnetic polarizing agents (PAs) that are added to the mixture to provide the source of electron spin polarization required for DNP. Here, we show that relatively high 1H DNP enhancements (∼60) can also be obtained in water without glycerol (or other glass forming agents) simply by dissolving high concentrations of electrolytes (such as NaCl or LiCl), which perturb the otherwise unavoidable ice crystallization observed upon cooling, thereby reducing PA phase separation and restoring DNP efficiency.

Insights into Glyphosate Adsorption in Aqueous Solutions Using Zn-Al Layered Double Oxide

AbstractContamination of surface and groundwater with glyphosate, used widely on crops to control weeds, can cause severe environmental damage. Processes for glyphosate removal from water bodies have been developed, but few are effective and all are expensive. This objective of the present study was to investigate the use of a layered double oxide as a potentially effective and inexpensive material to remove glyphosate from water. Equilibrium, kinetics, and adsorption mechanisms were evaluated, in addition to the effects of competing anions and temperature on glyphosate adsorption. Up to 95% of glyphosate was removed from a synthetic solution in 50 min by Zn2Al-LDO (layered double oxide in Zn/Al ratio of 2:1) at pH 10. The adsorption isotherms were type L and the Langmuir model best fitted the experimental data, with a qmax value of 191.96 μg mg–1 at 25°C. The XRD pattern did not support the hypothesis of intercalation of glyphosate anions, whereas Fourier-transform infrared and solid-state 13C and 31P magic angle spinning nuclear magnetic resonance confirmed the adsorption of glyphosate anions on the Zn2Al-LDO surface, through carboxylate and phosphonate moiety interactions with end-on and side-on modes. The degree of removal of glyphosate increased with increasing temperature and decreased with increasing concentration of competing anions, with carbonate anions having the most prominent effect on the inhibition of glyphosate adsorption. The adsorption kinetics fitted a pseudo-first order law. Moreover, the intraparticle diffusion model suggested that the adsorption process depends on the formation and thickness of the film at the solution/solid interface.

A new route of production of the meso-porous chitosan with well-organized honeycomb surface microstructure from shrimp waste without destroying the original structure of native shells: Extraction, modification and characterization study

The highly active bio-polysaccharide based compound namely chitin and chitosan have been extracted from shrimp shell which usually expelled out extensively from food processing industries and considered as waste materials. However, by conducting demineralization, de-proteinization and deacetylation on it which could be a new route of production of valuable meso-porous chitosan that possesses a noteworthy well-organized honeycomb like surface microstructure which undoubtedly capable to form sustainable bio-composites. Whereas the honeycomb like microstructures showed a well-defined pore canals (Pc) and pore canal tubes (Pct) onto their surface. The samples were characterized via ATR-FTIR spectroscopy, High resolution SEM, AFM, EDX, XRD and 13C solid-state Cross-Polarization Magic Angle Spinning (CPMAS) NMR. The molecular weight(M‾v) of isolated chitin and chitosan were determined by viscosity and the values were 1.06 × 106(DPv = 5228), 1.8 × 104(DPv = 116) respectively besides degree of deacetylation (DDA) were measured by ATR-FTIR spectroscopy, CPMAS NMR, pH-metric titration and the values were 24&21 for chitin and 84&82 for chitosan. The results suggest that the shrimp shell waste is an attractive source of well-organized honeycomb like meso-porous chitin and chitosan with regular surface microstructures which might have a significant/potential application into the sustainable bio-composite formulation due to various industrial and biomedical sector indeed.

BCN materials with adjustable active sites as heterogeneous acid–base catalysts for Knoevenagel condensation reaction

The Knoevenagel condensation reaction is one of the most effective methods for the formation of C–C bonds. However, developing efficient heterogeneous catalysts for the Knoevenagel condensation reaction is imperative. In this study, a series of boron carbon nitride (BCN) catalysts with adjustable active sites were designed via molecular self-assembly and calcination-temperature adjustment. The BCN materials synthesized at a calcination temperature of 750 °C (BCN-750) had the largest number of active sites and exhibited excellent activity, with a yield of 96% in the condensation reaction of benzaldehyde and malononitrile in only 4 min at room temperature. The excellent catalytic activity was attributed to the B and N species at the B–N–C sites, which functioned as acids and bases, respectively, to catalyze the Knoevenagel condensation reaction. This result was confirmed by temperature-programmed desorption of CO2 (CO2 TPD), temperature-programmed desorption of NH3 (NH3 TPD), X-ray photoelectron spectroscopy (XPS), and 11B solid-state magic-angle spinning nuclear magnetic resonance spectroscopy. In addition, aromatic and aliphatic aldehydes were successfully converted into their corresponding products. Analysis of the catalytic mechanism revealed that the deprotonation of malononitrile to form a carbanion was the rate-determining step.

Serial Polarization Transfer by Combination of Cross-Relaxation and Rotational Resonance for Sensitivity-Enhanced Solid-State NMR.

Methods which induce site-specificity and sensitivity enhancement in solid-state magic-angle spinning NMR spectroscopy become more important for structural biology due to the increasing size of molecules under investigation. Recently, several strategies have been developed to increase site specificity and thus reduce signal overlap. Under dynamic nuclear polarization (DNP) for NMR signal enhancement, it is possible to use cross-relaxation transfer induced by select dynamic groups within the molecules which is exploited by SCREAM-DNP (Specific Cross Relaxation Enhancement by Active Motions under DNP). Here, we present an approach where we additionally reintroduce the homonuclear dipolar coupling with rotational resonance (R2) during SCREAM-DNP to further boost the selectivity of the experiment. Detailed analysis of the polarization buildup dynamics of 13C-methyl polarization source and 13C-carbonyl target in 2-13C-ethyl 1-13C-acetate provides information about the sought-after and spurious transfer pathways. We show that dipolar-recoupled transfer rates greatly exceed the DNP buildup dynamics in our model system, indicating that significantly larger distances can be selectively and efficiently hyperpolarized.

Deep insight into reactive chemical structures of Class F fly ash

Reactive amorphous aluminum silicates dominate the reactivity of fly ash in alkali cement; however, the quantitative characterization of valid chemical compositions and structures information is highly challenging due to the heterogeneity and complexity of these phases. To acquire this information, in this work, Class F fly ash was treated with 1% hydrofluoric acid, followed by step-by-step analysis using a scanning electron microscope with an energy dispersive spectrometer (SEM-EDS), solid-state magic angle spinning nuclear magnetic resonance (MAS-NMR), and Fourier transform infrared (FT-IR) spectroscopy. Based on the acidolysis method, along with SEM-EDS statistical analysis, four amorphous aluminum silicate phases with relatively higher reactivity were successfully separated and quantitatively showcased, along with their respective average atomic percentage compositions (i.e., Si, Al, Ca, Fe, Na, K, and Mg%). In addition, the use of MAS-NMR and FT-IR analyses allowed for further quantitative insight into the reactive chemical structures and their associations with reactivity. The proposed characterization techniques have unique advantages for acquiring detailed reactive amorphous chemistries, which are difficult to obtain using conventional analysis procedures in alkali systems.

NMR spectroscopy-based analysis of gallstones of cancerous and benign gallbladders from different geographical regions of the Indian subcontinent.

Analysis of the chemical composition of gallstones is vital for the etiopathogenesis of gallstone diseases that can ultimately help in the prevention of its formation. In the present study, gallstones from seven different regions of India were analyzed to highlight the major difference in their composition. Also, gallstones of different pathological conditions i.e., benign (chronic cholecystitis, CC) and malignant gallbladder disease (gallbladder cancer GBC) were characterized. The type of polymorphs of cholesterol molecules was also studied to provide insight into the structure of gallstones. 1H solution state NMR spectroscopy 1D experiments were performed on a total of 94 gallstone (GS) samples collected from seven different geographical regions of India. Solid-State NMR spectroscopy 13C cross-polarization magic angle spinning (CPMAS) experiments were done on the 20 CC GS samples and 20 GBC GS samples of two regions. 1H NMR spectra from the solution state NMR of all the stones reveal that cholesterol was a major component of the maximum stones of the north India region while in south Indian regions, GS had very less cholesterol. 13C CPMAS experiments reveal that the quantity of cholesterol was significantly more in the GS of CC in the Lucknow region compared with GBC stones of Lucknow and Chandigarh. Our study also revealed that GS of the Lucknow region of both malignant and benign gallbladder diseases belong to the monohydrate crystalline form of cholesterol while GS of Chandigarh region of both malignant and benign gallbladder diseases exists in both monohydrate crystalline form with the amorphous type and anhydrous form. Gallstones have a complicated and poorly understood etiology. Therefore, it is important to understand the composition of gallstones, which can be found in various forms and clinical conditions. Variations in dietary practices, environmental conditions, and genetic factors may influence and contribute to the formation of GS. Prevention of gallstone formation may help in decreasing the cases of gallbladder cancer.

H-ZSM-5 Catalysts for the catalytic upcycling of polypropylene glycol

Without effective management, the steady increase of waste plastics threatens environmental well-being and ecological balance. Plastic up/recycling is a promising solution but has many challenges. In this work, catalytic cracking of polypropylene glycol (PPG) was investigated at varying reaction temperatures of 350–550 °C under nitrogen and steam, using H-ZSM-5 zeolites with different silica-to-alumina (SiO2/Al2O3) ratios of 23:1 and 50:1. The catalysts were assessed through physisorption, chemisorption, solid-state magic-angle spinning nuclear magnetic resonance spectrometry, thermogravimetry, electron microscopy, and positron annihilation lifetime spectroscopy. Extra framework aluminum and Lewis-to-Bronsted acid site ratios were found to play a significant role in the selectivity towards propionaldehyde, where values ∼ 80 % could be reached. In addition, a possible pathway for the PPG cracking reaction was proposed, which may lead to a better understanding of PPG and waste plastic decomposition via zeolite-based catalysts.

Cryogen-free 400 MHz (9.4 T) solid state MAS NMR system with liquid state NMR potential

We show that the temporal magnetic field distortion generated by the Cold Head operation can be removed and high quality Solid-State Magic Angle Spinning NMR results can be obtained with a cryogen-free magnet. The compact design of the cryogen-free magnets allows for the probe to be inserted either from the bottom (as in most NMR systems) or, more conveniently, from the top. The magnetic field settling time can be made as short as an hour after a field ramp. Therefore, a single cryogen-free magnet can be used at different fixed fields. The magnetic field can be changed every day without compromising the measurement resolution.

Understanding Lithium-Ion Dynamics in Single-Ion and Salt-in-Polymer Perfluoropolyethers and Polyethyleneglycol Electrolytes Using Solid-State NMR

Lithium metal batteries with high energy densities can enable a revolution in energy storage and accelerate shifts in electric transportation and electricity generation. However, several morphological and electro-chemo-mechanical challenges impede their development. Solid-state electrolytes such as those based on polymers show great promise in replacing liquid electrolytes in lithium metal batteries. Polyether-based polymer electrolytes are the most investigated but are plagued by low room-temperature ionic conductivity and poor oxidative stability. Hence, there is great need for the development and understanding of ion transport in new classes of polymer electrolytes. Perfluoropolyether (PFPE)-based electrolytes have shown improved oxidative stability, but little is understood about their lithium solvation and transport mechanism. In this work, we use multinuclear solid-state magic angle spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy to investigate the lithium cation environment and mobility in crosslinked single-ion and salt-in-polymer PFPE electrolytes and compare it directly to that of well-known polyethylene glycol (PEG) electrolytes. We show that the interaction of the lithium cation with the polymer backbone is weaker in PFPE systems compared to PEG, likely resulting in stronger ion pairing in the PFPE systems. Line shape analyses show lower lithium mobility in PFPE electrolytes despite lower activation energies being derived from spin-lattice relaxation (T1) measurements as compared to those for the PEG systems. The rapid relaxation is instead ascribed to the local fluctuations caused by polymer backbone mobility. By studying different modes of ion binding (single-ion vs salt-in-polymer), we show that differences across polymer backbones (PFPE vs PEG) have a greater effect on mobility than differences in ion binding modes within each polymer class (especially when single-ion conducting site density is not high). Our ability to use MAS NMR to study polymer electrolytes in their native state opens new opportunities to develop and understand novel polymer or hybrid solid-state electrolytes for next-generation lithium metal batteries.

The effect of 1H offset and flip-angle on heteronuclear decoupling efficiency in ROSPAC pulsed sequence: A Floquet description.

A new heteronuclear decoupling sequence for solid-state NMR and magic angle spinning faster than 60kHz was recently introduced [Simion et al., J. Chem. Phys. 157, 014202 (2022)]. It was dubbed ROtor-Synchronized Phase-Alternated Cycles (ROSPAC), and it offers robustness for a large range of chemical shifts and low radio-frequency (RF) powers and is almost independent of the radio-frequency power. Here, we theoretically explore the robustness of the ROSPAC sequence toward 1H offset and RF field inhomogeneities, as well as the spacing effect of the π pulses on the decoupling efficiency. We use a generalized theoretical framework based on the Floquet theory to assess these parameters. The optimum decoupling conditions, where the magnitude of the second-order cross-terms and first-order resonance conditions are small, were identified.

Arsenic(III) oxide intercalate with ammonium chloride: crystal structure revision and thermal characterization.

According to the crystal structure determination by Edstrand & Blomqvist [Ark. Kemi (1955), 8, 245-256], intercalate NH4Cl·As2O3·0.5H2O ({\bf Y_{{NH}_{4}Cl}}) is not isostructural with compound KCl·As2O3·0.5H2O. This is very unlikely because both NH4Br·2As2O3 and KBr·2As2O3 as well as NH4I·2As2O3 and KI·2As2O3 are isostructural. Hence, intercalate {\bf Y_{{NH}_{4}Cl}} has been studied using single-crystal X-ray diffraction in addition to attenuated total reflection Fourier transform infrared (ATR-FTIR) and 15N solid-state magic-angle spinning nuclear magnetic resonance (ssNMR) spectroscopies. These techniques indicate that revising the previous crystal structure model is necessary. Compound {\bf Y_{{NH}_{4}Cl}} crystallizes in space group P6/mmm with unit-cell parameters a = 5.25420 (10) Å and c = 12.6308 (3) Å and is isostructural with KCl·As2O3·0.5H2O. The presence of two symmetry-independent ammonium cations in the structure has been unequivocally confirmed using 15N ssNMR spectroscopy. The 15N ssNMR spectrum of intercalate {\bf Y_{{NH}_{4}Cl}} has been compared with analogous spectra of NH4Br·2As2O3 and NH4I·2As2O3 which allowed for a probable assignment of signals to ammonium cations occupying particular sites in the crystal structures. Thermogravimetry, differential scanning calorimetry and variable-temperature ATR-FTIR spectra have revealed that intercalate {\bf Y_{{NH}_{4}Cl}} is dehydrated between 320 and 475 K. Upon cooling or standing in moist air water is re-absorbed. Dehydration leads to significant shortening of the c unit-cell parameter as revealed by powder X-ray diffraction [c = 12.1552 (7) Å at 293 K]. Compound {\bf Y_{{NH}_{4}Cl}} decomposes on prolonged heating above 490 K to arsenic(III) oxide and ammonium chloride.

Exploring the Conformational Equilibrium of Mefenamic Acid Released from Silica Aerogels via NMR Analysis.

This study examines the influence of mefenamic acid on the physical and chemical properties of silica aerogels, as well as its effect on the sorption characteristics of the composite material. Solid state magic angle spinning nuclear magnetic resonance (MAS NMR) and high-pressure 13C NMR kinetic studies were conducted to identify the presence of mefenamic acid and measure the kinetic rates of CO2 sorption. Additionally, a high-pressure T1-T2 relaxation-relaxation correlation spectroscopy (RRCOSY) study was conducted to estimate the relative amount of mefenamic acid in the aerogel's pores, and a high-pressure nuclear Overhauser effect spectoscopy (NOESY) study was conducted to investigate the conformational preference of mefenamic acid released from the aerogel. The results indicate that mefenamic acid is affected by the chemical environment of the aerogel, altering the ratio of mefenamic acid conformers from 75% to 25% in its absence to 22% to 78% in the presence of aerogel.

Design of β-Alanine-Derived Novel C18 Stationary Phase Containing Embedded Urea and Amide Groups for the Separation of Versatile Analytes.

Novel stationary phases have been emerging recently. A β-alanine-derived embedded urea and amide group-containing C18 phase (Sil-Ala-C18) was prepared for the first time. The media were packed into a 150 × 2.1 mm HPLC column, and the newly designed column was evaluated with the Tanaka and Neue test protocols in reversed-phase liquid chromatography (RPLC) separation mode. Moreover, it was characterized by the Tanaka test protocol in hydrophilic interaction chromatography (HILIC) separation mode. The new phase was characterized by elemental analysis, attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and solid-state 13C cross-polarization magic angle spinning (CP/MAS) NMR spectroscopy at variable temperatures. The chromatographic evaluation involved very good separation of nonpolar shape-constrained isomers, polar and basic compounds in RPLC, and highly polar compounds in HILIC compared to the commercial reference columns. The Sil-Ala-C18 phase was able to separate the challenging β- and γ-isomers of tocopherol. The phase was also successfully applied for the separation of the isomers of tocopherol (vitamin E) and capsaicinoids from real samples of chili peppers (Capsicum spp.) in RPLC and ascorbic acid (vitamin C) in HILIC.

Potentially Health-Promoting Spaghetti-Type Pastas Based on Doubly Modified Corn Starch: Starch Oxidation via Wet Chemistry Followed by Organocatalytic Butyrylation Using Reactive Extrusion.

Extruded spaghetti-type pasta systems were obtained separately either from native or oxidized starch prepared via wet chemistry with the aim of evaluating the effect of oxidation modification of starch. In addition to this, the butyrylation reaction (butyrate (Bu) esterification-short-chain fatty acid) using native or oxidized starch was analyzed under reactive extrusion (REx) conditions with and without the addition of a green food-grade organocatalyst (l(+)-tartaric acid) with the purpose of developing potentially health-promoting spaghetti-type pasta systems in terms of increasing its resistant starch (RS) values. These would be due to obtaining organocatalytic butyrylated starch or not, or the manufacture of a doubly modified starch (oxidized-butyrylated-starch oxidation followed by organocatalytic butyrylation) or not. To this end, six pasta systems were developed and characterized by solid-state 13C cross-polarization magic angle spinning nuclear magnetic resonance (CP MAS NMR) spectroscopy, degree of substitution (DS), attenuated total reflectance Fourier transform infrared (ATR/FTIR) spectroscopy, X-ray diffraction (XRD), thermogravimetric analysis (TGA), pancreatic digestion, free Bu content analysis and in vitro starch digestibility. The results obtained here suggest that starch oxidation hydrolytically degrades starch chains, making them more susceptible to enzymatic degradation by α-amylase. However, the oxidized starch-based pasta systems, once esterified by Bu mainly on the amylose molecules (doubly modified pasta systems) increased their RS values, and this was more pronounced with the addition of the organocatalyst (maximum RS value = ~8%). Interestingly, despite the checked chemical changes that took place on the molecular structure of starch upon butyrylation or oxidation reactions in corn starch-based spaghetti-type pasta systems, and their incidence on starch digestibility, the orthorhombic crystalline structure (A-type starch) of starch remained unchanged.

Solid-state NMR spectroscopy at ultrahigh resolution for structural and dynamical studies of MOFs

To characterize the structure and dynamics of metal–-organic frameworks (MOFs) in-depth at the molecular level, it is necessary to pursue high-resolution solid-state magic angle spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy. Spectral resolution is usually affected by the quality of materials and various experimental conditions, of which magic angle (MA) accuracy is a crucial determinant. The current industrial criteria for MA calibration based on the common standard of KBr were found insufficient in guaranteeing optimal resolution MAS NMR for highly ordered MOFs. To drive towards higher-resolution MAS NMR spectroscopy, we propose a calibration protocol for more accurate MA with a higher-precision criterion based on 79Br MAS NMR of KBr, where the linewidth ratio of the fifth-order spinning sideband to the central band of KBr should be less than 1.00. As a result, ultrahigh-resolution 13C cross-polarization (CP) MAS NMR of MOF-5 is achieved with minimal linewidths as low as 4 Hz, and therefore MOF-5 can be used as a new standard convenient for verifying MA accuracy and also optimizing 13C CP conditions. Maintaining high-precision MA under variable temperature (VT) was found challenging on certain commercial MAS NMR probes, as was systematically investigated by VT NMR using KBr and MOF-5. Nevertheless, ultrahigh-resolution MAS NMR spectroscopy with stable MA under VT is employed to reveal fine structures and linker dynamics of a series of Zn-based MOFs with highly regulated structures. The ultrahigh-resolution NMR methodcan be generally applied to study a broad range of MOFs and other materials.

Elimination of A-234 from the environment: Effect of different decontaminants

With the fact that there are Novichoks in the list of toxic chemicals by the Chemical Weapons Convention parties, it is necessary to develop methods of effective neutralization of the agents as well as for other organophosphorus toxic substances. However, experimental studies on their persistence in the environment and effective decontamination measures remain scarce. Therefore, here, we investigated the persistence behavior and decontamination methods of A-234 (ethyl N-[1-(diethylamino)ethylidene]phosphoramidofluoridate), a Novichok series, A-type nerve agent to assess its potential risk to the environment. Different analytical methods were implemented, including 31P solid-state magic angle spinning nuclear magnetic resonance (NMR), liquid 31P NMR, gas chromatography-mass spectrometry (GC-MS), liquid chromatography-mass spectrometry, and vapor-emission screening using a microchamber/thermal extractor with GC-MS. Our results showed that A-234 is extremely stable in sand and poses a long-lasting risk to the environment even when released in trace quantities. Moreover, the agent is not easily decomposed by water, dichloroisocyanuric acid sodium salt, sodium persulfate, and chlorine-based water-soluble decontaminants. However, it is efficiently decontaminated by Oxone® monopersulfate, calcium hypochlorite, KOH, NaOH, and HCl within 30 min. Our findings provide valuable insights for eliminating the highly dangerous Novichok agents from the environment.