Solute-solvent interactions. VII. Proton magnetic resonance and infrared study of ion solvation in dipolar aprotic solvents

The solvation of a variety of ions by the dipolar aprotic solvents acetonitrile, sulfolane, and dimethylsulfoxide was studied through the influence of salts on the proton magnetic resonance chemical shifts of the solvents. In the case of acetonitrile the results were supplemented with infrared measurements, which showed that in general anions affect only the C–H and cations both the C–C and particularly the CN stretching frequencies of acetonitrile. The results are discussed in conjunction with transport and other data already in the literature. Current views on the structure of these solvents are summarized.From the Ph.D. thesis of this author, University of Pittsburgh, 1972.     

Hydrogen bonding interactions between indole and benzenoid-pi-bases

The NH-pi interactions of indole with benzene, naphthalene, phenanthrene, toluene, m-xylene, and mesitilene, in carbon tetrachloride solutions, have been studied by Fourier transform infrared spectroscopy. The experiments, carried out on the NH stretching band of indole, prove the formation of 1:1 complexes in which the NH bond of indole is engaged. The NH frequency shifts are independent of the number of rings in the base, but they progressively increase as the electron density is enhanced by methylation. The association constants increase with the increase of both, the number of rings and the methyl groups on the base. At higher base concentrations, further shifts on the free NH and associated bands indicate the formation of 1:2 complexes, which suggest hybride NH-pi and van der Waals interactions between one indole ring and two benzene acceptor molecules.     

Numerical and experimental studies of long-range magnetic dipolar interactions

We describe several numerical methods developed to analyze the behavior of spin polarized liquids in the presence of long-range magnetic dipolar interactions and external field gradients. Two of the methods use a discrete lattice of spins. In the first we calculate the magnetic field from the lattice of spins directly, either in the rotating frame, or in the lab frame. In the second method we include the dipolar fields from linear magnetization gradients analytically and calculate the dipolar fields from higher order gradients in Fourier space, where they are a local function of the magnetization. In the third method the magnetization is expanded in a Taylor series and the dipolar fields are calculated analytically for each term. The results of these calculations are compared to experimental data, in which we use two superconducting quantum interference device magnetometers adjacent to a spherical sample of hyperpolarized liquid 129Xe to detect the evolution of magnetization gradients. In particular, we observe an increase by a factor of 100 of the spin dephasing time in a longitudinal magnetic field gradient due to dipolar interactions of the spins. While each of the numerical techniques has certain limitations, they are generally in agreement with each other and with experimental data.     

Nuclear magnetic resonance studies on dipeptides

Dipeptides of different amino acids have been studied by NMR in aqueous solutions at different pH values. The results obtained are discussed in terms of the different contributions to the chemical shift of the α-CH protons.     

Nuclear magnetic resonance studies of hydrazyl radicals

A study of the nuclear magnetic resonance spectra of six hydrazyl radicals in solution, including α,α′-diphenyl-β-picryl-hydrazyl (DPPH), has been carried out. From the values of the paramagnetic shifts the constants (α_H) of hyperfine coupling with the protons were found. For DPPH these have the following values: On the basis of the analysis of the hyperfine constants a conclusion is drawn concerning the substantial role of σ-electron spin density delocalization in aromatic rings. The geometric structure of radicals investigated is also discussed in the paper.     

Nuclear magnetic resonance studies of chloroaluminate melts

Nuclear magnetic resonance has been used to study the structures of fused (Na, K)Al₂Cl₇ at 170°C. Sodium, aluminum and chlorine magnetic resonance, and proton magnetic resonance on substitution with NH₄⁺, indicate the structure to be essentially ionic as M⁺ Al₂Cl₇⁻.     

Nuclear magnetic resonance studies of resorcinol-formaldehyde aerogels

In this article, we report a detailed study of resorcinol-formaldehyde (RF) aerogels prepared under different processing conditions, [resorcinol]/[catalyst] (R/C) ratios in the starting sol-gel solutions, using continuous flow hyperpolarized (129)Xe NMR in combination with solid-state (13)C and two-dimensional wide-line separation (2D-WISE) NMR techniques. The degree of polymerization and the mobility of the cross-linking functional groups in RF aerogels are examined and correlated with the R/C ratios. The origin of different adsorption regions is evaluated using both coadsorption of chloroform and 2D EXSY (129)Xe NMR. A hierarchical set of Xe exchange processes in RF aerogels is found using 2D EXSY (129)Xe NMR. The exchange of Xe gas follows the sequence (from fastest to slowest): mesopores with free gas, gas in meso- and micropores, free gas with micropores, and, finally, among micropore sites. The volume-to-surface-area (V(g)/S) ratios for aerogels are measured for the first time without the use of geometric models. The V(g)/S parameter, which is related both to the geometry and the interconnectivity of the pore space, has been found to correlate strongly with the R/C ratio and exhibits an unusually large span: an increase in the R/C ratio from 50 to 500 results in about a 5-fold rise in V(g)/S.     

Nuclear magnetic resonance studies of adsorbed polymer layers

Nuclear magnetic resonance spectroscopy (NMR) encompasses a large range of techniques which can probe both the structure and dynamics of materials in detail. Of particular interest to the study of polymer adsorption is the ability to distinguish adsorbed segments (trains) from free segments (loops and tails) in a quantitative way. This may he achieved by a variety of experimental approaches and the background to those will be discussed. A brief overview of the necessary NMR theory will be given but for a more detailed treatment, the reader is referred to the large number of texts available [1].     

Nuclear magnetic resonance relaxation studies of polyacrylamide solution

 The cohesive interaction among polymer chains in a polyacrylamide (PAAm)–D₂O solution has been studied by NMR relaxation. The NMR relaxation times of PAAm in the good solvent D₂O were measured at different temperatures. The results show that the solution system has a high local viscosity and that its relaxation characteristic is soft-solid-like. The temperature dependence of the relaxation behavior of the solution is obviously different from that of ordinary polymer solutions. The difference lies in the relaxation behavior of the methylene protons in the main chain of PAAm, as shown by analyzing the relaxation process with single exponential and biexponential decays. As the temperature increases, the solvation is weakened, leading polymer chains to form curling coils, thus hindering the movement of the methylene protons among the main chains. It can be expected from the existence of 80% fast-relaxing protons that there are a zhigh number of entanglements among the polymer chains in PAAm solution. The information about entanglements among the polymer chains can be deduced from the biexponential dependence of the spin–spin relaxation on the concentration of the polymer solutions. Received: 14 April 1999/Accepted in revised form: 12 October 1999     

Nuclear magnetic resonance microscopy studies of membrane biofouling

There is a substantial need for novel measurement techniques that enable non-invasive spatially resolved observation of biofouling in nanofiltration (NF) and reverse osmosis (RO) membrane modules. Such measurements will enhance our understanding of the key design and operational parameters influencing biofilm fouling. In this study we demonstrate the first application of nuclear magnetic resonance microscopy (NMR) to a spiral wound reverse osmosis (RO) membrane module. The presented NMR protocols allow the extraction of the evolution with biofouling of (i) the spatial biofilm distribution in the membrane module, (ii) the spatially resolved velocity field and (iii) displacement propagators, which are distributions of molecular displacement of a passive tracer (in our case, water) in the membrane. From these measurements, the effective membrane surface area is quantified. Despite the opaque nature of membrane design, NMR microscopy is shown to be able to provide a non-invasive quantitative measurement of RO membrane biofouling and its impact on hydrodynamics and mass transport. Minimal biofilm growth is observed to have a substantial impact on flow field homogeneity.     

Nuclear magnetic resonance studies of helical dipyrromethene-zinc complexes

[formula: see text] Analysis of helical chirality within dinuclear dipyrromethene-Zn(II) complexes has been achieved with the use of 1H NMR spectroscopy. The use of AgFOD and chiral lanthanide shift reagents gives fully resolved resonances attributable to two diastereomeric helical complexes.     

Nuclear quadrupole resonance studies of structural and magnetic phase transitions

From the temperature dependence study of halogen NQR frequencies, various structural phase transitions have been reported for methylammonium hexahalometallates (IV) and tetramethylammonium hexachlorometallates (IV). These phase transitions and also those of the related compounds are collected and discussed by referring to the results of ¹H NMR and DTA measurements. We have studied several transition metal complexes, mainly copper (II) complexes, by NQR and found magnetic phase transitions from a paramagnetic to a magnetically ordered state, the existence of which has been confirmed by magnetic susceptibility measurements. These results are reviewed.     

Nuclear magnetic triple resonance studies on formamide-14N

The magnitudes of the two spin-spin coupling constants J(N¹H …? ¹³C), and all relatives signs of the couplings J(¹H …? ¹H) and J(¹H …? ¹³C) of formamide-¹⁴N, were determined by triple resonance experiments of the types ¹H—{¹³C}—{¹⁴N} and ¹H—{¹H}—{¹⁴N}.     

Nuclear magnetic resonance spectroscopic method for the estimation of competitive equilibrium constants

A nuclear magnetic resonance method is described which yields precise estimates of competitive equilibrium constants for systems in which two or more complexing agents compete for common species. Chemical-shift data under rapid exchange conditions are required, but neither analytical not equilibrium concentrations are needed. The method is demonstrated by estimating equilibria of proton exchange between aniline and pyridinium ion, proton exchange between triethylamine and diisopropylammonium ion, and cyclohexaamylose exchange between m- and p-hydroxybenzoic acids. The precisions of the equilibrium constants are similar to or better than those obtained from classical methods and are relatively free from interferences.     

Nuclear magnetic resonance spectroscopic studies of the trihexyl (tetradecyl) phosphonium chloride ionic liquid mixtures with water

Tetra-alkyl Phosphonium ionic liquids are phosphonium salts with melting points near room temperature. We report the NMR studies of water-trihexyl (tetradecyl) phosphonium chloride ionic liquid mixtures. The proton chemical shifts were used to investigate the intermolecular interactions in mixtures of ionic liquids and water. The OH chemical shifts were found to decrease as the water concentration in the ionic liquid increased, and their rate of change with temperature decreased with water concentration. The CH₂ and CH₃ chemical shifts were found to move downfield with the increase in temperature, and moved further downfield as water concentration was decreased. The interface of experimental data and the results of quantum calculations suggest a significant binding of phosphonium cations to chloride anion and water molecules. As well, the analysis of the data suggests a possible transformation from cationchloride-water configuration at low water concentrations to cation-water-water at higher water concentrations. Electronic Supplementary Material  Supplementary material is available for this article at and is accessible for authorized users.     

Hydrogen bonding NH/pi interactions between betacarboline and methyl benzene derivatives

In the presence of benzene, toluene, m-xylene, mesitylene and durene, the pyrrolic NH stretching band of betacarboline, 9H-pyrido[3,4-b]indole, and its 1-methyl derivative, harmane, in tetrachloroethane diminishes in intensity while a new red-shifted band grows up. The shifts of the associated bands increase linearly with the pi-electron density of the substrates. These spectral changes are attributed to the formation of 1:1 molecular association complexes between the betacarbolines and the benzenoid substrates. The complexes are stabilized by the hydrogen-bonding interaction between the pyrrolic NH group of betacarboline and the pi-delocalized electrons of the benzene derivatives. The influence of these NH/pi hydrogen-bonding interactions in the fluorescence spectra of betacarboline is discussed.     

Nuclear magnetic resonance and optical absorption spectroscopic studies on paramagnetic praseodymium(III) complexes with beta-diketone and heterocyclic amines

The optical absorption spectra of [Pr(acac)(3)(H(2)O)(2)].H(2)O, [Pr(acac)(3)phen.H(2)O] and [Pr(acac)(3)bpy] (where acac is the anion of acetylacetone, phen is 1,10-phenanthroline and bpy is 2,2'-bipyridyl) have been analyzed in the visible region in a series of non-aqueous solvents (methanol, ethanol, isopropanol, chloroform, acetonitrile and pyridine). The complexes display four non-hypersensitive 4f-4f transitions ((3)P(2), (3)P(1)+(1)I(6), (3)P(0) and (1)D(2)) from the (3)H(4) ground state. The band shape of the transitions shows remarkable changes upon dissolving in different solvents. Distinctively different band shapes have been observed for phen and bpy complexes. The phen is more effective in producing changes and the splitting of the bands is more pronounced in phen complex since it is a stronger ligand and leads to stronger Pr-N(phen) bond. The splitting of the bands is indicative of partaking of f-orbitals in bonding. The NMR signals of heterocyclic amines have been shifted to high fields while the resonances due to acetylacetone moiety have moved to low fields which is the consequence of change in geometry of the complexes upon coordination of the heterocyclic amines and reflects the importance of geometric factor (3cos(2)theta-1) in changing sign of the shift and to a good approximation the shifts arise predominantly from the dipolar mechanism. The phen complexes have narrower line width than bpy complexes. The line broadening in the case of bpy complexes is suggestive of exchange between inter-converting forms. The bpy possesses some degree of rotational freedom about C(6)-C(6') bond and the two pyridine rings undergo scissoring motion with respect to each other.