Study of liquid–liquid interfaces by an easily implemented localized NMR sequence

To selectively extract heavy metals from solutions containing fission products, it is essential to optimize the liquid–liquid extraction processes. Such an objective requires improving the fundamental knowledge of the different mechanisms that are involved in these processes. In that respect, we propose a localized NMR sequence named LOCSY to assess the concentration profiles of different species involved in these processes. One of the goals of this sequence is to study the products as close as possible to the liquid–liquid interface with the help of a standard NMR spectrometer of chemistry labs. The one‐dimensional spatial localization along the NMR tube is obtained by a discrete stepping of the frequency‐selective excitation pulses under a pulsed field gradient. Specific data processing has been developed to obtain the 1D NMR spectra as a function of the vertical position in the NMR tube. The LOCSY sequence has been tested and evaluated on three different systems: (i) a cylindrical phantom inserted in the NMR tube containing 4‐methylsalicylic acid solution, (ii) D₂O/olive oil biphasic system, and (iii) the dissolution of solid saccharose in D₂O. These examples illustrate potential applications of the LOCSY sequence, particularly the possibility to measure concentration profiles and to study phenomena such as diffusion, provided the dynamic range is compatible with NMR timescale and sensitivity. Copyright © 2010 John Wiley & Sons, Ltd.     

Self‐diffusion in a hyaluronic acid–albumin–water system as studied by NMR

Hyaluronic acid (HA) is an anionic biopolymer that is present in many tissues and can be involved in cancerous neoformations. HA can form complexes with proteins (particularly, serum albumin) in the body. However, HA structures and processes involving HA have not been extensively studied by NMR because the molecule's rigid structure makes these studies problematic. In the current work, self‐diffusion of HA and bovine serum albumin (BSA), and water in solutions was measured by ¹H pulsed field gradient NMR (PFG NMR) with a focus on the HA‐BSA‐D₂O systems at various concentrations of BSA and HA. It was shown that in the presence of even a small amount of HA, the self‐diffusion coefficient (SDC) of BSA decreases. To explain this fact, three hypotheses were proposed and analyzed. The first one was based on the effect of slowing down of water mobility in the presence of HA. The second hypothesis suggested an effect of mechanical collisions of BSA with HA molecules. The third hypothesized that BSA and HA molecules form a complex where BSA molecules reduced in mobility. It was shown that the third mechanism is the most likely. The state of the BSA molecules in the BSA‐HA‐D₂O system corresponds to a ‘fast exchange’ condition from the NMR point of view: BSA molecules reside in the ‘free’ and ‘bound’ (with HA) states for much shorter time than the diffusion time of the PFG NMR experiment, 7 ms. The fractions of ‘bound’ BSA molecules in the BSA‐HA complex were estimated. Copyright © 2012 John Wiley & Sons, Ltd.     

ITQ-3分子筛中二元混合分子扩散性质的模拟

采用平衡分子动力学方法先是模拟研究了纯组分Ar、SF_6以及CF4在ITQ-3分子筛中的扩散行为,结果表明,在窄孔道中Ar的扩散系数随负载的增加呈现先增加再减小的变化趋势,在宽孔道中则随负载逐渐减小。纯组分的大分子SF_6以及CF4只在y方向扩散,扩散系数与小分子在z方向的变化规律一致。随后,又模拟了二元混合组分SF_6和CF4在ITQ-3分子筛中的扩散行为,模拟结果与各自纯组分SF_6和CF4进行了对比,发现二元混合的SF_6和CF4整体变化趋势与其单组分保持一致,在y方向的扩散系数都是随着负载的增加而先增大后减小,但是两者之间还存在一种相互作用,使得在整个负载范围内扩散较快的CF4的扩散系数比纯组分的扩散系数相对小一些,而纯组分时扩散相对缓慢的SF_6在二元混合中的扩散系数则相对增大。     

Single-Scan Diffusion-Ordered NMR Spectroscopy of SABRE-Hyperpolarized Mixtures

The analysis of complex mixtures of dissolved molecules is a major challenge, especially for systems that gradually evolve, e. g., in the course of a chemical reaction or in the case of chemical instability. 1D NMR is a fast and non-invasive method suitable for detailed molecular analysis, though of low sensitivity. Moreover, the spectral resolution of proton, the most commonly used and most sensitive stable isotope in NMR, is also quite limited. Spatially encoded (SPEN) experiments aim at creating in one acquisition a 2D data set by simultaneously performing different 1D sub-experiments on different slices of the NMR tube, at the price of an extra loss of sensitivity. Choosing translational diffusion coefficients as the additional dimension (the so-called DOSY approach) helps to recover proton spectra of each molecule in a mixture. The sensitivity limitation of SPEN NMR can, on the other hand, be addressed with hyperpolarization methods. Within hyperpolarization methods, signal amplification by reversible exchange (SABRE), based on parahydrogen, is the cheapest and the easiest one to set up, and allows multi-shot experiments. Here we show that the spectra of a mixture's components at millimolar concentration are resolved in few seconds by combining the SABRE, SPEN and DOSY concepts.     

Assessment of techniques for DOSY NMR data processing

Diffusion-ordered spectroscopy (DOSY) NMR is based on a pulse-field gradient spin-echo NMR experiment, in which components experience diffusion. Consequently, the signal of each component decays with different diffusion rates as the gradient strength increases, constructing a bilinear NMR data set of a mixture. By calculating the diffusion coefficient for each component, it is possible to obtain a two-dimensional NMR spectrum: one dimension is for the conventional chemical shift and the other for the diffusion coefficient. The most interesting point is that this two-dimensional NMR allows non-invasive “chromatography” to obtain the pure spectrum for each component, providing a possible alternative for LC-NMR that is more expensive and time-consuming. Potential applications of DOSY NMR include identification of the components and impurities in complex mixtures, such as body fluids, or reaction mixtures, and technical or commercial products, e.g. comprising polymers or surfactants.

Data processing is the most important step to interpret DOSY NMR. Single channel methods and multivariate methods have been proposed for the data processing but all of them have difficulties when applied to real-world cases. The big challenge appears when dealing with more complex samples, e.g. components with small differences in diffusion coefficients, or severely overlapping in the chemical shift dimension. Two single channel methods, including SPLMOD and continuous diffusion coefficient (CONTIN), and two multivariate methods, called direct exponential curve resolution algorithm (DECRA) and multivariate curve resolution (MCR), are critically evaluated by simulated and real DOSY data sets. The assessments in this paper indicate the possible improvement of the DOSY data processing by applying iterative principal component analysis (IPCA) followed by MCR-alternating least square (MCR-ALS).     

Detection of Potential TNA and RNA Nucleoside Precursors in a Prebiotic Mixture by Pure Shift Diffusion‐Ordered NMR Spectroscopy

In the context of prebiotic chemistry, one of the characteristics of mixed nitrogenous‐oxygenous chemistry is its propensity to give rise to highly complex reaction mixtures. There is therefore an urgent need to develop improved spectroscopic techniques if onerous chromatographic separations are to be avoided. One potential avenue is the combination of pure shift methodology, in which NMR spectra are measured with greatly improved resolution by suppressing multiplet structure, with diffusion‐ordered spectroscopy, in which NMR signals from different species are distinguished through their different rates of diffusion. Such a combination has the added advantage of working with intact mixtures, allowing analyses to be carried out without perturbing mixtures in which chemical entities are part of a network of reactions in equilibrium. As part of a systems chemistry approach towards investigating the self‐assembly of potentially prebiotic small molecules, we have analysed the complex mixture arising from mixing glycolaldehyde and cyanamide, in a first application of pure shift DOSY NMR to the characterisation of a partially unknown reaction composition. The work presented illustrates the potential of pure shift DOSY to be applied to chemistries that give rise to mixtures of compounds in which the NMR signal resolution is poor. The direct formation of potential RNA and TNA nucleoside precursors, amongst other adducts, was observed. These preliminary observations may have implications for the potentially prebiotic assembly chemistry of pyrimidine threonucleotides, and therefore of TNA, by using recently reported chemistries that yield the activated pyridimidine ribonucleotides.     

An NMR study of methanol diffusion in polymer electrolyte fuel cell membranes

Methanol diffusion in two polymer electrolyte membranes, Nafion 117 and BPSH 40 (a 40% disulfonated wholly aromatic polyarylene ether sulfone), was measured using a modified pulsed field gradient NMR method. This method allowed for the diffusion coefficient of methanol within the membrane to be determined while immersed in a methanol solution of known concentration. A second set of gradient pulses suppressed the signal from the solvent in solution, thus allowing the methanol within the membrane to be monitored unambiguously. Over a methanol concentration range of 0.5–8 M, methanol diffusion coefficients in Nafion 117 were found to increase from 2.9 × 10⁻⁶ to 4.0 × 10⁻⁶ cm² s⁻¹. For BPSH 40, the diffusion coefficient dropped significantly over the same concentration range, from 7.7 × 10⁻⁶ to 2.5 × 10⁻⁶cm² s⁻¹. The difference in diffusion behavior is largely related to the amount of solvent sorbed by the membranes. Increasing the methanol concentration results in an increase in solvent uptake for Nafion 117, while BPSH 40 actually excludes the solvent at higher concentrations. In contrast, diffusion of methanol measured via permeability measurements (assuming a partition coefficient of 1) was lower (1.3 × 10⁻⁶ and 6.4 × 10⁻⁷ cm² s⁻¹ for Nafion 117 and BPSH 40 respectively) and showed no concentration dependence. The differences observed between the two techniques are related to the length scale over which diffusion is monitored and the partition coefficient, or solubility, of methanol in the membranes as a function of concentration. For the permeability measurements, this length is equal to the thickness of the membrane (178 and 132 μm for Nafion 117 and BPSH 40 respectively) whereas the NMR method observes diffusion over a length of approximately 4–8 μm. Regardless of the measurement technique, BPSH 40 is a greater barrier to methanol permeability at high methanol concentrations.     

Friction coefficients in self-diffusion,velocity sedimentation,and mutual diffusion for poly(ethylene oxide) in aqueous solution

The concentration dependences of the friction coefficient(s) for poly(ethylene oxide) have been determined on well-defined fractions in dilute aqueous solution. Three independent techniques have been used: FT-pulsed field gradient NMR (self-diffusion), photon correlation spectrosccpy (mutual diffusion), and velocity sedimentation, in the concentration range 1-25 kg m^?3. The results establish that, at a given concentration, the friction coefficient in self-diffusion is appreciably smaller than that operating in mutual diffusion and sedimentation; the friction coefficient in the latter processes are identical within experimental error.     

Diffusion with molecular association in chloroform + triethylamine and chloroform + dioxane mixtures

The Taylor dispersion method is used to measure the binary mutual diffusion coefficients of chloroform + triethylamine and chloroform +1,4-dioxane at 25°C. The components of these mixtures associate, forming chloroform-triethylamine and chloroform-dioxane, (chloroform)₂-dioxane molecular complexes. A modified Hartley-Crank equation is developed to express the binary diffusion coefficient as a weighted average of the diffusion coefficients of the free molecules and the molecular complexes. Counterintuitively, the contribution made by each molecular complex to the overall diffusion coefficient vanishes when the concentration of the complex reaches its maximum value. The measured and fitted diffusion coefficients agree within 3% or better over the complete composition range.     

Nanoparticle‐Assisted Affinity NMR Spectroscopy: High Sensitivity Detection and Identification of Organic Molecules

A simple and effective method for high‐sensitivity NMR detection of selected compounds is reported. The method combines 1D NMR diffusion filter experiments and small monolayer‐protected nanoparticles as high‐affinity receptors. Once bound to the nanoparticles, the diffusion coefficient of the analyte decreases in such way that spectral editing based on diffusion filters can separate its signals from those of other mixture components. Using nanoparticles functionalized with Zn²⁺‐triazacyclonane complexes, detection and identification of phosphorylated organic molecules can be achieved. Diphenyl phosphate can be detected at 25 micromolar concentration with good selectivity. The selectivity toward organic carboxylates is enhanced at pD=3.75. In these conditions, commercial tablets containing betamethasone phosphate and a large excess of benzoate could be successfully analyzed.     

Time-Resolved Diffusion NMR Measurements for Transient Processes

A general procedure for measurement of time-resolved diffusion coefficients of molecular species by NMR is described, including the use of methanol for fast temperature-independent gradient calibration.     

Studies on supramolecular gel formation using DOSY NMR

Herein, we present the results obtained from our studies on supramolecular self‐assembly and molecular mobility of low‐molecular‐weight gelators (LMWGs) in organic solvents using pulsed field gradient (PFG) diffusion ordered spectroscopy (DOSY) NMR. A series of concentration‐dependent DOSY NMR experiments were performed on selected LMWGs to determine the critical gelation concentration (CGC) as well as to understand the behaviour of the gelator molecules in the gel state. In addition, variable‐temperature DOSY NMR experiments were performed to determine the gel‐to‐sol transition. The PFG NMR experiments performed as a function of gradient strength were further analyzed using monoexponential DOSY processing, and the results were compared with the automated Bayesian DOSY transformation to obtain 2D plots. Our results provide useful information on the stepwise self‐assembly of small molecules leading to gelation. We believe that the results obtained from these experiments are applicable in determining the CGC and gel melting temperatures of supramolecular gels. Copyright © 2015 John Wiley & Sons, Ltd.     

Kinetics of the grating formation in holographic polymer-dispersed liquid crystals: NMR measurement of diffusion coefficients

Polymer films with embedded liquid crystal inclusions (polymer-dispersed liquid crystals) are superb composites for addressable windows, flexible displays and optical storage. Their scattering behavior and electro-optic properties depend essentially on the shape and size of the liquid crystal inclusions, which are typically formed by phase separation from a multicomponent homogeneous mixture. Here, pulsed field gradient NMR is used to measure the self-diffusion coefficients of the liquid crystal and a photo-reactive monomer, which compose such a precursor mixture. The kinetics of holographic grating formation in this mixture can be predicted by inserting the NMR diffusion coefficient of the monomer and the polymerization rate in a reaction diffusion model. The ratio of diffusion rate over reaction rate is found to be in the limiting regime in which the kinetics of the grating formation is not sensitive to this parameter.     

Diffusion Spectrum of Polymer Melt Measured by Varying Magnetic Field Gradient Pulse Width in PGSE NMR

The translational motion of polymers is a complex process and has a big impact on polymer structure and chemical reactivity. The process can be described by the segment velocity autocorrelation function or its diffusion spectrum, which exhibit several characteristic features depending on the observational time scale—from the Brownian delta function on a large time scale, to complex details in a very short range. Several stepwise, more-complex models of translational dynamics thus exist—from the Rouse regime over reptation motion to a combination of reptation and tube-Rouse motion. Accordingly, different methods of measurement are applicable, from neutron scattering for very short times to optical methods for very long times. In the intermediate regime, nuclear magnetic resonance (NMR) is applicable—for microseconds, relaxometry, and for milliseconds, diffusometry. We used a variation of the established diffusometric method of pulsed gradient spin-echo NMR to measure the diffusion spectrum of a linear polyethylene melt by varying the gradient pulse width. We were able to determine the characteristic relaxation time of the first mode of the tube-Rouse motion. This result is a deviation from a Rouse model of polymer chain displacement at the crossover from a square-root to linear time dependence, indicating a new long-term diffusion regime in which the dynamics of the tube are also described by the Rouse model.     

NMR chromatography using microemulsion systems

NMR spectroscopy is an excellent tool for structural analysis of pure compounds. However, for mixtures, it performs poorly because of overlapping signals. Diffusion ordered NMR spectroscopy (DOSY) can be used to separate the spectra of compounds with widely differing molecular weights, but the separation is usually insufficient. NMR "chromatographic" methods have been developed to increase the diffusion separation but these usually introduced solids into the NMR sample that reduce resolution. Using nanostructured dispersed media, such as microemulsions, eliminates the need for suspensions of solids and brings NMR chromatography into the mainstream of NMR analytical techniques. DOSY was used in this study to resolve spectra of mixtures with no increase in line-width as compared to regular solutions. Components of a mixture are differentially dissolved into the separate phases of the microemulsions. Several examples of previously reported microemulsions and those specifically developed for this purpose were used here. These include a fully dilutable microemulsion, a fluorinated microemulsion, and a fully deuterated microemulsion. Log(diffusion) difference enhancements of up to 1.7 orders of magnitude were observed for compounds that have similar diffusion rates in conventional solvents. Examples of commercial pharmaceutical drugs were also analyzed via this new technique, and the spectra of up to six components were resolved from one sample.     

Predicting gas transport in formed zeolite adsorbents from NMR studies

The self-diffusion of nitrogen, methane, and carbon monoxide within a 5A zeolitic adsorbent has been examined with use of pulsed field gradient (PFG) NMR. In all cases, the diffusion process is well-described by a refined version of the long-range diffusion model (LRDM), adapted here for use with pelletized adsorbents, which uses exclusively adsorbent porosity and isotherm data as inputs. Correlation of the experimental data with this model yields tortuosity factors that are characteristic of the adsorbate and reflect the longer diffusive path a molecule must take due to the winding nature of the pore structure. It is demonstrated that the diffusion model can be used to accurately predict the diffusion coefficients for a ternary gas mixture within a 5A zeolite. To fully characterize the diffusive process, the surface excess on the PFG NMR samples has been obtained by a novel gas-phase NMR technique that is well-suited for measuring pure and multicomponent isotherms.     

Infrared Diffusion-Ordered Spectroscopy Reveals Molecular Size and Structure**

Inspired by ideas from NMR, we have developed Infrared Diffusion-Ordered Spectroscopy (IR-DOSY), which simultaneously characterizes molecular structure and size. We rely on the fact that the diffusion coefficient of a molecule is determined by its size through the Stokes–Einstein relation, and achieve sensitivity to the diffusion coefficient by creating a concentration gradient and tracking its equilibration in an IR-frequency resolved manner. Analogous to NMR-DOSY, a two-dimensional IR-DOSY spectrum has IR frequency along one axis and diffusion coefficient (or equivalently, size) along the other, so the chemical structure and the size of a compound are characterized simultaneously. In an IR-DOSY spectrum of a mixture, molecules with different sizes are nicely separated into distinct sets of IR peaks. Extending this idea to higher dimensions, we also perform 3D-IR-DOSY, in which we combine the conformation sensitivity of femtosecond multi-dimensional IR spectroscopy with size sensitivity.     

Identification of partially disordered peptide intermediates through residue-specific NMR diffusion measurements

It is technically challenging to detect low-population partially disordered species that are in equilibrium with the folded and unfolded states. Residue-specific translational diffusion experiments measured by pulsed field gradient NMR have been used to detect the presence, and define the conformation, of such equilibrium intermediates. The experiment is demonstrated for equilibrium solutions of related triple helical peptides that model a small region of type I collagen with and without a mutation known to cause osteogenesis imperfecta. The data show that residue-specific diffusion coefficients of an interconverting trimer to monomer system can allow discrimination between a simple two-state model and more complex multistate models involving partially disordered intermediates.     

Diffusion of molecules confined in semipenetrable nanoscale carriers probed by pulsed field gradient NMR

Diffusion of three low-molecular-weight compounds cyclohexane (CX), benzene (BZ), and chloroform (CL) preferentially confined in the cores of nanoscale carriers was probed by pulsed field gradient (PFG) NMR methods. The carriers were monolayer micelles of sodium dodecyl sulfate (SDS), bilayer micelles of poly(hexyl methacrylate)-block-(acrylic acid) (M2), and trilayer micelles of poly(2-ethylhexyl methacrylate)-block-(methyl methacrylate)-block-(acrylic acid) (M3) in D(2)O at 300 K. Although the radius of the confinement space was 10(-)(8) m or lower, the course of the PFG signal attenuation in pulsed gradient spin-echo or stimulated echo experiments under varied diffusion time corresponds to apparently unrestricted diffusion, which is slowed down compared to that of the compound dissolved in D(2)O. Analysis using approximate relations reveals that the response of the system to PFG NMR consists of three independent components, namely (i) diffusion of the carrier as a whole, (ii) hindered escape of a confined molecule and its diffusion in the medium, and (iii) diffusion of the molecules dissolved in the medium. If process ii is fast enough, exchange of the compound between the carrier and the medium includes the influence of iii as a component of a monoexponential PFG decay; otherwise, two sets of signals are observed with different diffusion responses, or biexponential PFG is observed. According to the results of this study, the only barrier of the diffusion of the inspected compounds CX, BZ, and CL out of their confinement in the carriers SDS or M2 is a thermodynamic one, that is, the resistance of the saturated solution to accept surplus molecules of the solute. In a three-layer micelle M3, the additional polymer sheet around the confinement area forms an additional diffusion barrier for CX, however. The study shows that PFG NMR, though unable to observe directly restricted diffusion on the nanoscale, can be useful in studying systems designed, for example, for a controlled release of low-molecular-weight substances.     

Ionic diffusion and salt dissociation conditions of lithium liquid crystal electrolytes

Salt dissociation conditions and dynamic properties of ionic species in liquid crystal electrolytes of lithium were investigated by a combination of NMR spectra and diffusion coefficient estimations using the pulsed gradient spin-echo NMR techniques. Activation energies of diffusion (Ea) of ionic species changed with the phase transition of the electrolyte. That is, Ea of the nematic phase was lower than that of the isotropic phase. This indicates that the aligned liquid crystal molecules prepared efficient conduction pathways for migration of ionic species. The dissociation degree of the salt was lower compared with those of the conventional electrolyte solutions and polymer gel electrolytes. This is attributed to the low concentration of polar sites, which attract the dissolved salt and promote salt dissociation, on the liquid crystal molecules. Furthermore, motional restriction of the molecules due to high viscosity and molecular oriented configuration in the nematic phase caused inefficient attraction of the sites for the salt. With a decreased dissolved salt concentration of the liquid crystal electrolyte, salt dissociation proceeded, and two diffusion components attributed to the ion and ion pair were detected independently. This means that the exchange rate between the ion and the ion pair is fairly slow once the salt is dissociated in the liquid crystal electrolytes due to the low motility of the medium molecules that initiate salt dissociation.