Impact of NH4OH treatment on the ion exchange and pore characteristics of a metakaolin-based geopolymer.

We investigated the viability and influence of NH4OH post-synthetic treatment on the pore characteristics of geopolymers. Geopolymers are a class of materials with amorphous aluminosilicate three-dimensional frameworks, regarded as amorphous analogues of zeolites. Similar to zeolites, when geopolymers are used in catalysis or adsorption applications, post-synthetic treatments such as ion exchange with NH4 + salts (e.g., NH4Cl and NH4NO3) and desilication (using strong bases such as NaOH) are necessary to introduce active sites and modify their pore structure, respectively. Recently, it has been shown that treatment with NH4OH combines these two steps, in which acidic sites are introduced and the pore structures of zeolites are modified simultaneously. Considering the increasing interest in geopolymers in catalysis and adsorption applications, understanding the impact of such treatment on the structure of geopolymers is needed. Our diffuse reflectance infrared Fourier-transform spectra show that NH4 + exchanges Na+ in the geopolymer, and laser diffraction with scanning electron microscopy images show that the particle size of the powdered geopolymer decreases after NH4OH treatment. N2 sorption isotherms and 129Xe and 1H NMR measurements revealed information about the changes in pore structures: micropores were larger than mesopores and inborn mesopores increased in diameter, thereby reducing the surface area to volume ratio. However, pore accessibility and pore connectivity were not altered by NH4OH treatment. Since solid-state NMR and X-ray fluorescence revealed desilication, these changes in particle size and pore characteristics are considered to be due to desilication caused by NH4OH treatment.

Gas Uptake and Thermodynamics in Porous Liquids Elucidated by 129Xe NMR.

We exploited 129Xe NMR to investigate xenon gas uptake and dynamics in a porous liquid formed by dissolving porous organic cages in a cavity-excluded solvent. Quantitative 129Xe NMR shows that when the amount of xenon added to the sample is lower than the amount of cages present (subsaturation), the porous liquid absorbs almost all xenon atoms from the gas phase, with 30% of the cages occupied with a Xe atom. A simple two-site exchange model enables an estimate of the chemical shift of 129Xe in the cages, which is in good agreement with the value provided by first-principles modeling. T2 relaxation times allow the determination of the exchange rate of Xe between the solvent and cage sites as well as the activation energies of the exchange. The 129Xe NMR analysis also enables determination of the free energy of confinement, and it shows that Xe binding is predominantly enthalpy-driven.

SPICY: a method for single scan rotating frame relaxometry.

T 1ρ is an NMR relaxation mode that is sensitive to low frequency molecular motions, making it an especially valuable tool in biomolecular research. Here, we introduce a new method, SPICY, for measuring T1ρ relaxation times. In contrast to conventional T1ρ experiments, in which the sequence is repeated many times to determine the T1ρ time, the SPICY sequence allows determination of T1ρ within a single scan, shortening the experiment time remarkably. We demonstrate the method using 1H T1ρ relaxation dispersion experiments. Additionally, we combine the sequence with spatial encoding to produce 1D images in a single scan. We show that T1ρ relaxation times obtained using the single scan approach are in good agreement with those obtained using the traditional experiments.

Insights into the role of molar ratio and added water in the properties of choline chloride and urea-based eutectic mixtures and their cellulose swelling capacity.

Eutectic mixtures and deep eutectic solvents (DESs) are promising green media for the pre-treatment of lignocellulose materials. They can be harnessed for the swelling of cellulose and further facilitate cellulose hydrolysis, derivatization, and production of cellulose-based (nano) materials. Several studies indicated that water can take part in the formation of the nanostructure of DES; however, it is still unclear how additional water influences many important properties and functioning of DES, especially when the molar ratio of compounds differs from the eutectic point composition. Here, viscosity, pH, conductivity, solvatochromic and solvatomagnetic solvent parameters, and fiber swelling capacity of choline chloride and urea mixtures demonstrating different molar ratios were investigated in the presence and absence of added water. The participation of water in the formation of molecular clusters with choline chloride and urea was indicated by viscosity, pH, and conductivity measurements. Hydrogen bond acceptor values of aqueous mixtures increased as a function of water content, and the results obtained using both methods were in line, indicating their suitability for the determination of hydrogen bond acidity of aqueous choline chloride-urea mixtures. However, hydrogen bond basicity determined by solvatochromic and magnetic methods exhibited almost opposite trends. The close investigation of the chemical shift of solvatomagnetic probes indicated that the chemical environment of the choline chloride-urea (1 : 2) mixture remained constant until the water content of 30 wt% was in line with previous molecular simulations. When cellulose fibers were treated with mixtures under mixing, the non-ideality of the choline chloride-urea mixture and the absence of water were found to be advantageous; however, aqueous mixtures efficiently increased the diameters of cellulose fibers in the absence of mixing, and water-containing mixtures appeared to be appealing systems for cellulose pretreatments.

Aqueous Modification of Chitosan with Itaconic Acid to Produce Strong Oxygen Barrier Film.

In this study, the chemical modification of chitosan using itaconic acid as a natural-based unsaturated dicarboxylic acid was investigated. In an aqueous environment, the amine group of chitosan reacts with itaconic acid to produce a chitosan derivative with pyrrolidone-4-carboxylic acid group. On the basis of the elemental analysis, 15% of the amine groups of chitosan reacted, thus creating modified chitosan with amine and carboxylic acid functionalities. Due to the presence of amine and carboxylic acid groups, the surface charge properties of the chitosan were notably altered after itaconic acid modification. In an aqueous solution, the modified chitosan exhibited zwitterionic properties, being cationic at low pH and turning anionic when the pH was increased over 6.5, whereas the original chitosan remained cationic until pH 9. Furthermore, it was demostrated that the modified chitosan was suitable for the preparation of a self-standing film with similarly high transparency but notably higher mechanical strength and oxygen barrier properties compared to a film made from the original chitosan. In addition, the thermal stability of the modified chitosan film was higher than that of the original chitosan film, and the modified chitosan exhibited flame-retardant properties.

Comparison of Lignin Fractions Isolated from Wheat Straw Using Alkaline and Acidic Deep Eutectic Solvents.

This study aims to examine the characteristics of two solid lignin fractions isolated from wheat straw using alkaline and acidic deep eutectic solvents (DESs). The chemical properties and morphological characteristics of the two lignin fractions were evaluated by measuring their purity, elemental composition, molecular weight and particle size distributions, and microstructure. Their chemical structure was evaluated using DRIFT (diffuse reflectance infrared Fourier transform) spectroscopy, GPC (gel permeation chromatography), TGA (thermogravimetric analysis), 13C NMR (nuclear magnetic resonance), 31P NMR, and HSQC NMR. Our findings showed that the lignin isolated using alkaline DESs was less pure and had a smaller particle size, higher molecular weight, and thermal stability compared to the lignin isolated using acidic DESs. Their lignin structure was also determined to be different due to varying selective fractures on the linkages of lignin. These results suggest that the DES treatments could selectively extract lignin from wheat straw with different yields, compositions, morphologies, and structures, which could then provide a theoretical basis for the selection of DESs for specially appointed lignin extraction.

Direct magnetic-field dependence of NMR chemical shift.

Nuclear shielding and chemical shift are considered independent of the magnetic-field strength. Ramsey proposed on theoretical grounds in 1970 that this may not be valid for heavy nuclei. Here we present experimental evidence for the direct field dependence of shielding, using 59Co shielding in Co(acac)3 [tris(acetylacetonate)cobalt(iii)] as an example. We carry out NMR experiments in four field strengths for this low-spin diamagnetic Co(iii) complex, which features a very large and negative nuclear shielding constant of the central Co nucleus. This is due to a magnetically accessible, low-energy eg ← t2g orbital excitation of the d6 system. The experiments result in temperature-dependent magnetic-field dependence of -5.7 to -5.2 ppb T-2 of the 59Co shielding constant, arising from the direct modification of the electron cloud of the complex by the field. First-principles multiconfigurational non-linear response theory calculations verify the sign and order of magnitude of the experimental results.

Low-Concentration Measurements of Nuclear Spin-Induced Optical Rotation Using SABRE Hyperpolarization.

Nuclear spin-induced optical rotation (NSOR) is a promising phenomenon for molecular structure elucidation due to its sensitivity to electronic structure near atomic nuclei. It is the only experimentally verified nuclear magneto-optic effect (NMOE), so far observed usually in neat liquids or in concentrated binary mixtures, with the proportion of the minor component at least 10%. We report a method to extend the lower-concentration range of NSOR measurements by 2 orders of magnitude by employing continuous-flow SABRE (signal amplification by reversible exchange) hyperpolarization. This approach significantly increases the sensitivity of NSOR and enables its detection in dilute samples, as demonstrated with measurements of NSOR of 90 mmol/L solutions of pyridine and pyrazine. The results are compared with first-principles calculations, and good agreement is found. The possibility to measure low-concentration solutions significantly extends the pool of samples available for further studies of NMOEs.

High-throughput continuous-flow system for SABRE hyperpolarization.

Signal Amplification By Reversible Exchange (SABRE) is a versatile method for hyperpolarizing small organic molecules that helps to overcome the inherent low signal-to-noise ratio of nuclear magnetic resonance (NMR) measurements. It offers orders of magnitude enhanced signal strength, but the obtained nuclear polarization usually rapidly relaxes, requiring a quick transport of the sample to the spectrometer. Here we report a new design of a polarizing system, which can be used to prepare a continuous flow of SABRE-hyperpolarized sample with a considerable throughput of several millilitres per second and a rapid delivery into an NMR instrument. The polarizer performance under different conditions such as flow rate of the hydrogen or liquid sample is tested by measuring a series of NMR spectra and magnetic resonance images (MRI) of hyperpolarized pyridine in methanol. Results show a capability to continuously produce sample with dramatically enhanced signal over two orders of magnitude. The constant supply of hyperpolarized sample can be exploited, e.g., in experiments requiring multiple repetitions, such as 2D- and 3D-NMR or MRI measurements, and also naturally allows measurements of flow maps, including systems with high flow rates, for which the level of achievable thermal polarization might not be usable any more. In addition, the experiments can be viably carried out in a non-deuterated solvent, due to the effective suppression of the thermal polarization by the fast sample flow. The presented system opens the possibilities for SABRE experiments requiring a long-term, stable and high level of nuclear polarization.

Ultrafast multidimensional Laplace NMR for a rapid and sensitive chemical analysis.

Traditional nuclear magnetic resonance (NMR) spectroscopy relies on the versatile chemical information conveyed by spectra. To complement conventional NMR, Laplace NMR explores diffusion and relaxation phenomena to reveal details on molecular motions. Under a broad concept of ultrafast multidimensional Laplace NMR, here we introduce an ultrafast diffusion-relaxation correlation experiment enhancing the resolution and information content of corresponding 1D experiments as well as reducing the experiment time by one to two orders of magnitude or more as compared with its conventional 2D counterpart. We demonstrate that the method allows one to distinguish identical molecules in different physical environments and provides chemical resolution missing in NMR spectra. Although the sensitivity of the new method is reduced due to spatial encoding, the single-scan approach enables one to use hyperpolarized substances to boost the sensitivity by several orders of magnitude, significantly enhancing the overall sensitivity of multidimensional Laplace NMR.

Cholesterol under oxidative stress-How lipid membranes sense oxidation as cholesterol is being replaced by oxysterols.

The behavior of oxysterols in phospholipid membranes and their effects on membrane properties were investigated by means of dynamic light scattering, fluorescence spectroscopy, NMR, and extensive atomistic simulations. Two families of oxysterols were scrutinized-tail-oxidized sterols, which are mostly produced by enzymatic processes, and ring-oxidized sterols, formed mostly via reactions with free radicals. The former family of sterols was found to behave similar to cholesterol in terms of molecular orientation, roughly parallel to the bilayer normal, leading to increasing membrane stiffness and suppression of its membrane permeability. In contrast, ring-oxidized sterols behave quantitatively differently from cholesterol. They acquire tilted orientations and therefore disrupt the bilayer structure with potential implications for signaling and other biochemical processes in the membranes.

Detection of phase biaxiality in liquid crystals by use of the quadrupole shift in 131Xe NMR spectra.

An experimental method to unambiguously distinguish between uniaxial and biaxial liquid crystal phases is introduced. The method is based on the second order quadrupole shift (SOQS) observable in 131Xe NMR spectra of xenon dissolved in liquid crystals. It is shown that besides revealing the biaxiality, the 131Xe SOQS offers a novel method to determine the tilt angle in smectic C phases. As an example, the 131Xe SOQS in a ferroelectric liquid crystal is reported. It yields up a biaxial phase in between isotropic and smectic C phases.

Carbon and proton shielding tensors in methyl halides.

The series of methyl halides, CH(3)X (X = F, Cl, Br, and I), is prototypic for demonstrating the s.c. normal halogen dependence of light-atom nuclear magnetic resonance shielding constants in the presence of halogen atoms of varying electronegativity. We report a systematic experimental and first-principles theoretical study of the (13)C and (1)H shielding tensors in this series. The experimental shielding constants were obtained from gas-phase NMR experiments and the anisotropies were determined using liquid crystal NMR spectroscopy. After taking into account rovibrational effects and solute-solvent interactions, this provided the currently best experimental estimates for the full shielding tensors. Quantum chemical calculations were carried out at ab initio and density functional theory levels, involving relativistic corrections taken into account at the leading-order Breit-Pauli perturbation level. Anharmonic and harmonic vibrational corrections were performed. The main trends of the shielding constants and anisotropies of the nearby light (13)C and (1)H nuclei as functions of the halogen mass, were confirmed to be mainly due to relativistic spin-orbit effects. For carbon, also the scalar relativistic effects are important for quantitative results. Thermal averaging at 300 K decreases the magnitude of all the parameters but exhibits partial cancellation between the nonrelativistic and smaller relativistic rovibrational averages. For the shielding anisotropy, the relativistic terms add to the negative rovibrational effect. Overall, the current experimental and theoretical results are in excellent agreement for all the shielding parameters, setting a standard for further investigations of normal halogen dependence.

NMR measurements and density functional calculations of the 199Hg-13C spin-spin coupling tensor in methylmercury halides.

The isotropic average, JisoHgC, and the anisotropy, DeltaJHgC, of the 199Hg-13C spin-spin coupling tensor in methylmercury halides, CH3HgX (X=Cl, Br, I), were determined for the first time by utilizing the NMR spectra of these molecules dissolved in liquid crystals. Furthermore, density functional calculations were performed using the zeroth-order regular approximation, including also dimethylmercury. The temperature-dependence of the JisoHgC couplings in the isotropic phase was studied in each case in order to extrapolate their values into the liquid crystal state. Good agreement is found between the experimental and the calculated DeltaJHgC values as long as solvent effects are considered in the computations. Most of the magnitude of DeltaJ can be attributed to the spin mechanism of J-coupling, with additional sizable spin-orbital cross terms due to electronic spin-orbit coupling.

Dual probe fluorescence monitoring of intracellular free calcium during ischemia in mouse heart by using continuous compensation for pH dependence of the dissociation constant of Fura-2, and the interference of myoglobin.

Mitochondrial damage is the main source of cellular injury upon ischemia-reperfusion, and calcium loading has been implicated in this phenomenon. The use of optical probes for calcium monitoring of the intact heart is hampered by internal filter effects of intracellular hemoproteins, endogenous fluorescence, and their sensitivity to pH. We describe here a method for measurement of intracellular free calcium in isolated myoglobin-deficient perfused mouse hearts under conditions of large intracellular pH fluctuations by simultaneous fluorescence monitoring of the calcium-probe Fura-2 and the pH probe BCECF through dual wavelength excitation of both probes. In myoglobin-containing mouse heart endogenous chromophores interfere with Fura-2 fluorometry. It is shown that a paradoxical decrease in Fura-2 fluorescence occurs during ischemia in isolated mouse hearts. Simultaneous recording of BCECF fluorescence (calibrated against pH measurement with phosphorus NMR) and data reduction based on continual recalculation of the apparent dissociation constant of the calcium-probe complex revealed that a marked increase in intracellular free calcium occurs, and that the Fura-2 fluorescence decrease was caused by an increase in dissociation constant due to intracellular acidification. Intracellular free calcium rose almost linearly during a 20-min period of ischemia and returned to basal values rapidly upon the commencement of perfusion.

Experimental and quantum-chemical determination of the (2)H quadrupole coupling tensor in deuterated benzenes.

Deuterium Quadrupole Coupling Constant (DQCC) in benzene was determined both experimentally by Nuclear Magnetic Resonance spectroscopy in Liquid Crystalline solutions (LC NMR) and theoretically by ab initio electronic structure calculations. DQCCs were measured for benzene-d(1) and 1,3,5-benzene-d(3) using several different liquid crystalline solvents and taking vibrational and deformational corrections into account in the analysis of experimental dipolar couplings, used to determine the orientational order parameter of the dissolved benzene. The experimental DQCC results for the isotopomers benzene-d(1) and 1,3,5-benzene-d(3) are found to be 187.7 kHz and 187.3 kHz, respectively, which are essentially equal within the experimental accuracy (+/-0.4 kHz). Theoretical results were obtained at different C-D bond lengths, and by applying corrections for electron correlation and rovibrational motion on top of large-basis-set Hartree-Fock results. The computations give a consistent DQCC of ca. 189 kHz for three different isotopomers; benzene-d(1), 1,3,5-benzene-d(3), and benzene-d(6), revealing that isotope effects are not detectable within the present experimental accuracy. Calculations carried out using a continuum solvation model to account for intermolecular interaction effects result in very small changes as compared to the data obtained in vacuo. The comparison of theoretical and experimental results points out the selection of the underlying molecular geometry as the most likely source of the remaining discrepancy of less than 2 kHz. Such an agreement between the calculated and the experimental DQCC results can only be achieved if rovibrational effects are considered on one hand in the experimental direct dipolar coupling data, and on the other hand in the theoretical property calculation, as is done presently.

Relativistic spin-orbit coupling effects on secondary isotope shifts of (13)C nuclear shielding in CX(2) (X = O, S, Se, Te).

Rovibrational corrections, temperature dependence, and secondary isotope shifts of the (13)C nuclear shielding in CX(2) (X = O, S, Se, Te) are calculated taking into account the relativistic spin-orbit (SO) interaction. The SO effect is considered for the first time for the secondary isotope shifts. The nuclear shielding hypersurface in terms of nuclear displacements is calculated by using a density-functional theory method. Ab initio multiconfiguration self-consistent field calculations are done at the equilibrium geometry for comparison. (13)C NMR measurements are carried out for CS(2). The calculated results are compared with both present and earlier experimental data on CO(2), CS(2), and CSe(2). The heavy-atom SO effects on the rovibrational corrections of (13)C shielding are shown to be significant. For CSe(2) and CTe(2), reliable prediction of secondary isotope effects and their temperature dependence requires the inclusion of the SO corrections. In particular, earlier discrepancies of theory and experiment for CSe(2) are fully resolved by taking the SO interactions into account.