Search

A promising CO2 sorbent based on the [Emim][Gly]/silica gel composite has been studied. Absorption experiments have shown that the optimum loading of [Emim][Gly] ionic liquid in silica gel is 40 wt%. The 2-step process CO2 binding mechanism in [Emim][Gly] has been proposed based on the results of absorption experiments, 2H NMR spectroscopy and ab-initio calculations. The impact of CO2 on the microscopic viscosity and the dynamical melting of ionic liquid has been thoroughly investigated. 2H NMR spectroscopy has revealed that CO2 strongly binds cation and anion in [Emim][Gly], forcing them to move in a correlated fashion., (© 2024 Wiley‐VCH GmbH.)

The metal-organic frameworks (MOFs) attract interest as potential catalysts whose catalytic properties are driven by defects. Several methods have been proposed for the defects-inducing synthesis of MOFs. However, the active species formed on the defective sites remain elusive and uncharacterized, as the spectroscopic fingerprints of these species are hidden by the regular structure signals. In this work, we have performed the synthesis of ZIF-8 MOF with defect-inducing procedures using fully deuterated 2-methylimidazolate ligands to enhance the defective sites' visibility. By combining 1 H and 31 P MAS NMR spectroscopy and X-ray absorption spectroscopy, we have found evidence for the presence of different structural hydroxyl Zn-OH groups in the ZIF-8 materials. It is demonstrated that the ZIF-8 defect sites are represented by Zn-OH hydroxyl groups with the signals at 0.3 and -0.7 ppm in the 1 H MAS NMR spectrum. These species are of basic nature and may be responsible for the catalytic activity of the ZIF-8 material., (© 2024 Wiley-VCH GmbH.)

Metal-organic framework (MOF) glasses have emerged as a new class of organic-inorganic hybrid glass materials. Considerable efforts have been devoted to unraveling the macroscopic dynamics of MOF glasses by studying their rheological behavior; however, their microscopic dynamics remain unclear. In this work, we studied the effect of vitrification on linker dynamics in ZIF-62 by solid-state 2 H nuclear magnetic resonance (NMR) spectroscopy. 2 H NMR relaxation analysis provided a detailed picture of the mobility of the ZIF-62 linkers, including local restricted librations and a large-amplitude twist; these details were verified by molecular dynamics. A comparison of ZIF-62 crystals and glasses revealed that vitrification does not drastically affect the fast individual flipping motions with large-amplitude twists, whereas it facilitates slow cooperative large-amplitude twist motions with a decrease in the activation barrier. These observations support the findings of previous studies, indicating that glassy ZIF-62 retains permanent porosity and that short-range disorder exists in the alignment of ligands because of distortion of the coordination angle.

Observing and quantifying the like-charge attraction in liquids and solutions is still challenging. However, we showed that elusive cation-cation hydrogen bonding may govern the structure and interaction in hydroxyl-functionalized ionic liquids. Therefore, cationic cluster formation depends on the shape, charge distribution, and functionality of the ions. We demonstrated by means of solid-state 2 H NMR spectroscopy that cationic clusters change the structure and dynamics of ionic liquids. With increasing alkyl chain length, we observed two deuteron quadrupole coupling constants for the OD groups, differing by about 30 kHz. The lower value was assigned to the cation-cation interaction, indicating that the average (c-c) hydrogen bonds are stronger than the (c-a) hydrogen bonds between the cation and the anion despite the repulsive and attractive Coulomb interaction in the first and latter cases. Ion mobility could be studied by 2 H NMR spectroscopy, although the deuterons in the hydrogen-bonded clusters underwent fast exchange. Our results also showed that simple relaxation models are not applicable anymore and that anisotropic motion must be considered.

The UiO-66 (Zr) metal-organic framework (MOF) is of notable interest due to its facile synthesis, robustness under a wide range of chemical and physical conditions and its capability to separate industrially relevant hydrocarbons mixtures. However, the knowledge of the molecular mechanisms behind these process remains limited. Here, we present a combined experimental ( 2 H NMR) and computational study of the molecular mobility, transport and adsorption of C 5 alkanes isomers in a dehydroxylated UiO-66 (Zr) MOF. We show that the tetrahedral cages of the MOF are the preferred adsorption location for both n -pentane and isopentane. In a binary mixture of the isomers, isopentane interacts more strongly with the material leading it to occupy more of the tetrahedral cages than n -pentane, resulting in an isopentane/ n -pentane adsorption selectivity of α ads = 2 (at 373 K). At the same time, the microscopic diffusivity for n -pentane, D n ( E n = 18 kJ mol -1 ), is significantly lower than for isopentane, D iso ( E iso = 28 kJ mol -1 ), which results in a high separation selectivity for a n -pentane/isopentane mixture of α ≈ 13 (at 300 K). This shows that the UiO-66 MOF is indeed a promising active material for use in light hydrocarbon separation processes.

The adsorption method for atmospheric water harvesting (AWH) is considered as a promising heat-driven technology for potable water supply in arid regions. This research is focused on novel composite sorbents based on hygroscopic salts loaded in the pores of MIL-101(Cr) developed for AWH. The composites based on LiCl, LiBr, CaCl 2 , and Ca(NO 3 ) 2 were synthesized and comprehensively studied by SEM, XRD, N 2 adsorption, and thermogravimetric methods. We evidence that the CaCl 2 /MIL-101(Cr) composite demonstrates a high net water uptake of 0.52-0.59 g_(H 2 O)/g_(composite) per cycle under conditions of Saudi Arabia and the Sahara desert as the reference regions with extra-dry climate, which exceeds the appropriate values for other adsorbents. It is shown that water adsorption on the composite cannot be presented as a combination of the adsorption on the components, thus indicating a synergistic effect. A detailed characterization of water coordination, mobility, and hydrogen bonding within the confined CaCl 2 hydrates and salt solution using solid-state 2 H NMR spectroscopy has been performed. It is established that pore confinement promotes a prolonged transition to a dynamically melted state of the hydrated salt and a notable decrease of the melting temperature, which facilitates the molecular transport of water and causes the alteration of sorption properties of CaCl 2 inside MIL-101 pores. Finally, the performance of AWH employing CaCl 2 /MIL-101(Cr) was evaluated in terms of the fractions of water extracted and collected, and the specific energy consumption, demonstrating its high potential for AWH., (© 2023 The Authors. ChemSusChem published by Wiley-VCH GmbH.)

Attractive interactions between ions of like charge remain an elusive concept. Observing and quantifying this type of interaction in liquids and solutions is still a major challenge. Recently, we have shown that cation-cation interactions are present in hydroxyl-functionalized ionic liquids and that they can be controlled by the shape, charge distribution and functionality of the ions. In the present study, we demonstrate that cationic cluster formation does not only change the local structures of the ionic liquids but also influences the dynamics of the cations in a characteristic way. We show that solid-state 2 H NMR spectroscopy is well suited for the study of molecular motion, even if the hydrogen bonded species of interest are indistinguishable due to fast deuteron exchange. We also provide valuable information about the applicability of well-accepted relaxation models.

We report strong isotope effects for the protic ionic liquid triethylammonium methanesulfonate [TEA][OMs] by means of deuterium solid-state NMR spectroscopy covering broad temperature ranges from 65 K to 313 K. Both isotopically labelled PILs differ in non-deuterated and fully deuterated ethyl groups of the triethyl ammonium cations. The N-D bond of both cations is used as sensitive probe for hydrogen bonding and structural ordering. The 2 H NMR line shape analysis provides the deuteron quadrupole coupling constants and the characteristics of a broad heterogeneous phase with simultaneously present static and mobile states indicating plastic crystal behavior. The temperatures where both states are equally populated differ by about 80 K for the two PILs, showing that deuteration of the ethyl groups in the trialkylammonium cations tremendously shifts the equilibrium towards the static state. In addition, it leads to a significant less cooperative transition, associated with a significantly reduced standard molar transition entropy., (© 2022 The Authors. ChemPhysChem published by Wiley-VCH GmbH.)

We report the complex phase behavior of the glass forming protic ionic liquid (PIL) d3-octylphosphonium bis(trifluoromethylsulfonyl)imide [C 8 H 17 PD 3 ][NTf 2 ] by means of solid-state NMR spectroscopy. Combined line shape and spin relaxation studies of the deuterons in the PD 3 group of the octylphosphonium cation allow to map and correlate the phase behavior for a broad temperature range from 71 K to 343 K. In the solid PIL at 71 K, we observed a static state, characterized by the first deuteron quadrupole coupling constant reported for PD 3 deuterons. A transition enthalpy of about 12 kJ mol -1 from the static to the mobile state with increasing temperature suggests the breaking of a weak, charge-enhanced hydrogen bond between cation and anion. The highly mobile phase above 100 K exhibits an almost disappearing activation barrier, strongly indicating quantum tunneling. Thus, we provide first evidence of tunneling driven mobility of the hydrogen bonded P-D moieties in the glassy state of PILs, already at surprisingly high temperatures up to 200 K. Above 250 K, the mobile phase turns from anisotropic to isotropic motion, and indicates strong internal rotation of the PD 3 group. The analyzed line shapes and spin relaxation times allow us to link the structural and dynamical behavior at molecular level with the phase behavior beyond the DSC traces., (© 2022 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH.)

UiO-66 (Zr) is a metal-organic framework (MOF) known for its thermal and chemical stability and wide range of adsorption-based applications. This MOF exhibits high separation selectivity for butane isomers. It has been earlier inferred that the separation performance of the material depends on the hydroxylation state of the zirconia cluster. In this contribution, we apply 2 H solid-state NMR to characterize the dynamics of both the MOF organic framework itself and butane isomers in hydroxylated and dehydroxylated forms of UiO-66. It is established that the rate of π-flipping and the amplitude of the phenylene ring plane librations in the framework are higher for the dehydroxylated form. Self-diffusion coefficients of butane isomers have been estimated for both forms of UiO-66. The diffusivity is higher for n-butane in the dehydroxylated form, whereas the diffusion of isobutane is not affected by the presence of OH groups in the zirconia cluster of the MOF. Higher diffusivity of n-butane in dehydroxylated form is accounted for by the larger effective diameter of the window between the adjacent cages in this form, which arises from faster rotation and larger amplitude of framework linker libration. This rationalizes the higher efficiency of the dehydroxylated form of UiO-66(Zr) material for butane isomers separation., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)

We show that solid-state NMR spectroscopy is a suitable method for characterizing the structure, hydrogen bond dynamics and phase transition behavior in protic ionic liquids (PILs). Deuteron line shape and spin relaxation time analysis provide a description of the structural and dynamical heterogeneity in the solid state of the model PIL triethyl ammonium bis(trifluoromethanesulfonyl)amide [TEA][NTf 2 ]. Therein, we observed two deuteron quadrupole coupling constant for the ND bond of the TEA cation, indicating differently strong hydrogen bonds to the nitrogen and oxygen atoms of the NTf 2 anion, as we could confirm by DFT calculations. The transition processes in the dynamically heterogeneous phase are characterized by two standard molar enthalpies and thus different stages of melting. We provide geometry, rates and energetics of the cation in the solid and liquid states of the PIL. Comparison with PILs having stronger interacting anions shows higher enthalpy change between the solid and liquid states, lower activation barriers of tumbling motion and higher amplitude of librational motion for the TEA cation in the presence of the weakly interacting anion NTf 2 . We provide reasonable relations between microscopic and macroscopic properties, as is relevant for any kind of application.

The relationship between the adsorption of water on MIL-53 (Al) MOF, the structural phase of MIL-53 (Al), and the quadrupole coupling constant of 27 Al framework aluminium atom (QCC) of the MOF AlO 4 (OH) 2 centres (Al-sites) has been investigated by combining solid-state 27 Al MAS NMR spectroscopy with XRD analysis and DFT calculations. It is established that 27 Al QCC is primarily sensitive to water adsorption to the Al-sites and by a minor extent to the framework contraction/expansion interconversions. We thus conclude that the 27 Al MAS NMR method is sensitive enough to differentiate the effects of pore contractions and water adsorption to Al-sites basing on the changes of the QCC value.

The family of zeolitic-imidazole framework (ZIF) materials is currently considered for the challenging separation of C4 hydrocarbons. However, yet, the microscopic diffusion mechanism for these hydrocarbons in these narrow gate porous materials remains elusive by conventional methods due to its very slow nature. Experimental (solid-state 2 H nuclear magnetic resonance-NMR) and computational (molecular dynamics-MD) approaches were applied together to derive slow diffusional dynamics of n -butane and 1-butene in ZIF-8. By means of the 2 H NMR technique, we evidenced the presence of two adsorption sites for the guests localized inside the cages of ZIF-8 and in the vicinity of the gates. We characterized the molecular mobility at each site and revealed that the translational intercage diffusion is realized by a slow directional motion associated with the gate-crossing. MD simulations provide an in-depth analysis of the diffusion and fully support the proposed dynamics picture for both n -butane and 1-butene. These calculations enable the derivation of the diffusivity and barriers for the long-range diffusion of both hydrocarbons in ZIF-8 and unraveled the microscopic diffusion mechanism implying intracage and intercage motions. We show that this NMR approach combined with modeling is a valuable tool to probe the molecular mobility for slow diffusing species in ordered cagelike porous frameworks.

We present a detailed solid-state NMR characterization of the molecular dynamics of tert-butyl alcohol (TBA) confined inside breathing metal-organic framework (MOF) MIL-53(Al). 27 Al MAS NMR has demonstrated that TBA adsorption induces the iX phase of MIL-53 material with partially shrunk channels. 2 H solid-state NMR has shown that the adsorbed alcohol exhibits anisotropic rotations of the methyl groups around two C 3 axes and librations of the molecule as a whole about the axis passing through the TBA C-O bond. These librations are realized by two distinct ways: fast molecule orientation change during the translational jump diffusion along the channel with characteristic time τ D of about 10 -9  s at 300 K; slow local librations at a single coordination site, representing framework hydroxyl groups, with τ l ≈10 -6  s at 300 K. Self-diffusion coefficient of the alcohol in the MOF has been estimated: D=3.4×10 -10  m 2  s -1 at 300 K. It has been inferred that both the framework flexibility and the interaction with framework hydroxyl groups define the dynamics of TBA confined in the channels of MIL-53 (Al)., (© 2020 Wiley-VCH GmbH.)

We measured the deuteron quadrupole coupling constants (DQCCs) for hydroxy-functionalized ionic liquids (ILs) with varying alkyl chain length over the temperature range between 60 and 200 K by means of solid-state NMR spectroscopy. For all temperatures, the 2 H spectra show two DQCCs representing different types of hydrogen bonds. Higher values, ranging from 220 to 250 kHz, indicate weaker hydrogen bonds between cation and anion (c-a), and lower values varying from 165 to 210 kHz result from stronger hydrogen bonds between the OD groups of cations (c-c), in agreement with recent observations in infrared, neutron diffraction, and NMR studies. We observed different temperature dependencies for (c-a) and (c-c) hydrogen bonding. From the static pattern of the 2 H spectra at the lowest temperatures, we derived the true DQCCs being up to 20 kHz larger than recently reported values measured at the glass transition temperature. We were able to freeze the librational motions of the hydrogen bonds in the ILs. The temperature dependence of the (c-a) and (c-c) cluster populations in the glassy state is opposite to that observed in the liquid state, partly anticipating the behavior of ILs tending to crystallize.

In this study, a successful proton conduction modulation of MOFs, from an ionic insulator to an ionic conductor, is demonstrated through their structural transformation. It is shown that the reversible structural change from amorphous to crystalline phases allows for the reversible proton conduction modulation of MOFs. Moreover, the proton conduction mechanism of the ionic conductor phase is elucidated by 2 H NMR analysis.

Highly stable superprotonic conductivity (>10 -2 S cm -1 ) has been achieved through the unprecedented solvent-free- coordinative urea insertion in MOF-74 [M 2 (dobdc), M = Ni 2+ , Mg 2+ ; dobdc = 2,5-dioxido-1,4-benzenedicarboxylate] without an acidic moiety. The urea is bound to open metal sites and alters the void volume and surface functionality, which triggers a significant change in proton conductivity and diffusion mechanism. Solid-state 2 H NMR revealed that the high conductivity was attributed to the strengthening of the hydrogen bonds between guest H 2 O induced by hydrogen bonds in the interface between H 2 O and the polarized coordinated urea.

In hydroxy-functionalized ionic liquids, two types of hydrogen bonding coexist: the conventional H-bonds between cation and anion (c-a) and those between cation and cation (c-c), although the interaction between like-charged ions is supposed to be much weaker due to the repulsive Coulomb forces. Counting the cations involved in either (c-a) or (c-c) clusters is a challenge. For that purpose, we recently performed neutron diffraction (ND) measurements and molecular dynamics (MD) simulations at and above room temperature accompanied by NMR solid-state experiments in the glassy state of the ILs. In principle, these methods are suitable for determining the populations of (c-a) and (c-c) cluster species. For different reasons we could only address single temperatures and/or small temperature intervals above 300 K. The by far largest temperature range with reasonable efforts is accessible by simple infrared (IR) spectroscopy. However, counting (c-a) or (c-c) hydrogen bonds is a difficult task due to the different transition dipole moments resulting in varying intensities and broad vibrational bands. Here we present a method for deriving the number of cations involved in (c-a) ion pairs from IR spectra in the OH stretch region. This procedure provides access to the equilibria of (c-a) and (c-c) hydrogen bonds as a function of temperature allowing derivation of the transition enthalpy.

We present a detailed 2 H NMR characterization of molecular mobility of propene and propane propagating though the microporous ZIF-8, a zeolitic imidazolate framework renowned for its outstandingly high separation selectivity for industrially relevant propene/propane mixtures. Experimental characterization of both propene and propane diffusivity in ZIF-8 has been provided. Using 2 H NMR spin relaxation analysis, the motional mechanisms for propene and propane guests trapped within the ZIF-8 framework have been elucidated. Kinetic parameters for each type of motion were derived. The characteristic times for microscopic translational diffusion and activation barriers (E C3H8 = 38 kJ mol -1 , E C3H6 = 13.5 kJ mol -1 ) for propane and propene diffusivities have been estimated. A notable difference in the observed activation barriers emphasizes that the ZIF-8 window crossing is associated with the "gate-opening" and represents an extremely shape selective process. Finally, we show that the 2 H NMR technique is capable of providing reliable information on microscopic diffusivity in the ZIF-8 MOF even for molecules with slow diffusivity (<10 -14 m 2 s -1 ).

We present deuteron quadrupole coupling constants (DQCC) for hydroxyl-functionalized ionic liquids (ILs) in the crystalline or glassy states characterizing two types of hydrogen bonding: The regular Coulomb-enhanced hydrogen bonds between cation and anion (c-a), and the unusual hydrogen bonds between cation and cation (c-c), which are present despite repulsive Coulomb forces. We measure these sensitive probes of hydrogen bonding by means of solid-state NMR spectroscopy. The DQCCs of (c-a) ion pairs and (c-c) H-bonds are compared to those of salt bridges in supramolecular complexes and those present in molecular liquids. At low temperatures, the (c-c) species successfully compete with the (c-a) ion pairs and dominate the cluster populations. Equilibrium constants obtained from molecular-dynamics (MD) simulations show van't Hoff behavior with small transition enthalpies between the differently H-bonded species. We show that cationic-cluster formation prevents these ILs from crystallizing. With cooling, the (c-c) hydrogen bonds persist, resulting in supercooling and glass formation., (© 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.)

We show that deuteron quadrupole coupling constants (DQCCs), and reorientational correlation times of molecular bonds N-D that are involved in hydrogen bonding, can be determined from NMR T1 relaxation time experiments simultaneously. For this purpose, we used trialkylammonium-based protic ionic liquids (PILs) as model compounds. They exhibit high viscosities and wide liquid ranges that allow measurements far beyond the extreme narrowing region (ω0τc ≪ 1). The T1 minima already occur at temperatures significantly above room temperature. We obtain reasonable DQCCs for the liquid phase if anisotropic motion is considered. The DQCCs are very small due to attractive Coulomb interaction between the cation and anion, which is further enhanced by hydrogen bonding. The DQCCs strongly depend on the interaction strength of the anion but are independent of the alkyl chain length of the trialkyl ammonium cations pointing to the exclusive cation-anion interaction along the hydrogen bond.

Coordinatively unsaturated metal sites (CUS) play an important role in catalysis by metal-organic frameworks (MOF). Being an intrinsic part of the framework the CUS take the role of acidic sites active in industrially relevant processes such as condensation or oxidation reactions. The key step of such reactions represents the coordination of the reagents to CUS. In MOFs the mechanism of the reagent interaction with CUS is poorly understood. Herein, we characterize the interaction of a widely used acidity probe pyridine with CUS of MIL-100(Al) MOF by means of the 2 H solid-state NMR spectroscopy. 2 H NMR reveals that pyridine species, which are interacting with CUS and the ones which are coordinated to the Al-OH site, exhibit different motional behavior. 2 H NMR line shape as well as T 1 , T 2 relaxation analyses for [D 5 ]pyridine adsorbed in MIL-100(Al) allowed us to perform a detailed characterization of pyridine dynamics in both states including the kinetics of the exchange process between these adsorption states., (© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

We present investigation of the effect of electron-donor guests on framework mobility in the metal-organic framework (MOF) MIL-101(Cr) monitored by solid state 2 H NMR spectroscopy. In a guest-free material, the mobile phenylene fragments of the terephthalate (TP) linkers populate two fractions with notably different kinetic parameters for torsional motion. Two fractions of rotational motion are indicative of non-equivalence of TP linker binding to the Cr 3 O trimer, the primary building unit of the MIL-101 framework. It is established that the interaction of the guest molecules with coordinatively unsaturated metal sites (CUS) of the MOF dramatically decreases torsional barriers for the linker motions, enhancing the rotation rate. This result is opposite to a more conventional slowing down effect on the linker rotation of the guests not selectively interacting with the adsorption sites inside the framework of the MOFs. The effect of coordination on both the torsional barrier and the rotation rate depends notably on the particular guest interacting with the CUS. The found effects of the guest on the rotational motion represent a basis for developing the strategy for ruling and controlling the linker rotation in MOFs with CUS. It is shown that if water occupies CUS, another guest (tert-butanol, cyclohexanone) fails to competitively coordinate to the site., (© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

The heterogeneity in dynamics has important consequences for understanding the viscosity, diffusion, ionic mobility, and the rates of chemical reactions in technology relevant systems such as polymers, metallic glasses, aqueous solutions, and inorganic materials. Herein, we study the spatial and dynamic heterogeneities in ionic liquids by means of solid state NMR spectroscopy. In the 2 H spectra of the protic ionic liquid [TEA][OTf] we observe anisotropic and isotropic signals at the same time. The spectra measured below the melting temperature at 306 K could be simulated by a superposition of the solid and liquid line shapes, which provided the transition enthalpies between the rigid and mobile fractions. Consequently, we measured the spin-lattice relaxation times T 1 for the anisotropic and the isotropic signals for the temperature range between 203 and 436 K. Both dispersion curves could be fitted to models including rotational correlation times, activation barriers and rate constants. This approach allowed determining the rotational correlation times for the N-D molecular vector of the [TEA] + cation in differently mobile environments. The mobility is only slightly different, as indicated by small differences in activation energies for these processes. The NMR correlation times for the highly mobile phase are linearly related to measured viscosities, which supports the applicability of the Stokes-Einstein-Debye relation.

We present the first deuteron quadrupole coupling constants (DQCCs) for selected protic ionic liquids (PILs) measured by solid-state NMR spectroscopy. The experimental data are supported by dispersion-corrected density functional theory (DFT-D3) calculations and molecular dynamics (MD) simulations. The DQCCs of the N-D bond in the triethylammonium cations are the lowest reported for deuterons in PILs, indicating strong hydrogen bonds between ions. The NMR coupling parameters are compared to those in amides, peptides, and proteins. The DQCCs show characteristic behavior with increasing interaction strength of the counterion and variation of the H-bond motifs. We report the similar presence of the quadrupolar splitting pattern and the narrow liquid line in the NMR spectra over large temperature ranges, indicating the heterogeneous nature of PILs., (© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)