Multiple-quantum Magic-angle Spinning Research Articles

High-resolution heteronuclear correlations between spin-1/2 and half-integer quadrupolar nuclei under fast MAS solid-state NMR

High isotropic resolution is essential for the structural elucidation of samples with multiple sites. In this study, utilizing the benefits of TRAPDOR-based heteronuclear multiple quantum coherence (T-HMQC) and a pair of one rotor period long cosine amplitude modulated low-power (cos-lp) pulse-based symmetric-split-t1 multiple-quantum magic angle spinning (MQMAS) methods, we have developed a proton-detected 2D 35Cl/1H T-HMQC-MQMAS pulse sequence under fast MAS (70 kHz) to achieve high-resolution in the indirect dimension of the spin-3/2 (35Cl) nuclei connected via protons. As T-HMQC polarizes not only single-quantum central transition (SQCT) but also triple-quantum (TQ) coherences, the proposed 2D pulse sequence is implemented via selection of two coherence pathways (SQCT→TQ →SQCT and TQ → SQCT→TQ) resulting in the 35Cl isotropic dimension and is superior to the existing double-quantum satellite-transition (DQST) T-HMQC in terms of resolution.

Modulating hierarchical ZSM-5 crystals from etching-assisted growth with substituted phenols

The rational modulation of zeolite microstructures tailoring crystal morphology and hierarchy, is an effective way to promote their mass transport and catalytic performance. However, practical realization remains challenging. We recently demonstrated a novel etching-assisted crystallization process that allows fine control over zeolite architecture by eliminating intermediate defective nanocrystals with active proton-bearing organic molecules such as phenol. Here, we investigated in detail the phenolic etching effect on the crystallization of ZSM-5 zeolites using a combination of techniques including diffuse reflectance infrared Fourier-transform spectroscopy (DRIFTS) and 2D 27Al multiple quantum magic angle spinning nuclear magnetic resonance (MQ MAS NMR) and systematically elucidated the structure modulation with a homologous series of phenolic compounds. Time-series characterizations confirmed the initial seed formation, intermediate dissolution, and final perfected crystallization stages during ZSM-5 synthesis in the presence of phenolic compounds. Since deprotonation to phenolate anion in-situ is required during alkaline zeolite synthesis, the electron-withdrawing (EW) groups on the phenol para-position lead to bigger ZSM-5 crystals with more mesopores, while the phenolic molecules with para- electron-donating (ED) groups exhibit less significant effect. Under the same initial pH, the phenolic compounds show unparalleled compatibility with zeolite crystallization by stabilizing the system pH values, whereas inorganic acids invariably fail the zeolite crystallization. Given the remarkable kinetic control over zeolite growth through the simultaneous but opposite nucleophilic etching process, our observation provides a versatile way to manipulate zeolite crystallization with high tunability.

Cation and anion ordering in synthetic lepidolites and lithian muscovites: influence of the OH ∕ F and Li ∕ Al ratios on the mica formation studied by NMR (nuclear magnetic resonance) spectroscopy and X-ray diffraction

Abstract. A large number of lepidolites K(LixAl3−x)[Si2xAl4−2xO10](OH)yF2−y and Li-muscovites K(LixAl2-x/3□1-2x/3)[Si3AlO10](OH)yF2−y were synthesised by a gelling method in combination with hydrothermal syntheses at a pressure of 2 kbar and a temperature of 873 K. The nominal composition ranged between 0.0≤x≤2.0 and 0.0≤y≤2.0, i.e. from polylithionite K[Li2.0Al][Si4.0O10](OH)yF2−y over trilithionite K[Li1.5Al1.5][AlSi3.0O10](OH)yF2−y to muscovite K[Al2.0□][AlSi3.0O10](OH)yF2−y. 1H, 19F, 29Si and 27Al magic-angle spinning nuclear magnetic resonance (MAS NMR) and 27Al multiple-quantum magic-angle spinning (MQMAS) NMR spectroscopy has been performed to investigate the order and/or disorder state of Si and Al in the tetrahedral layers and of Li, Al, OH and F in the octahedral layer. The synthetic mica crystals are very small, ranging from 0.1 to 5 µm. With increasing Al content, the crystal sizes decrease. Rietveld structure analyses on 12 samples showed that nearly all samples consist of two mica polytypes (1M and 2M1) of varying proportions. In the case of lepidolites, the 1M / 2M1 ratio depends on the Li/Al ratio of the reaction mixture. The refinement of the occupancy factors of octahedral sites shows that lepidolites (1.5≤x≤2.0) represent a solid solution series with polylithionite and trilithionite as the endmembers. In the case of the Li-muscovites (0.0≤x≤1.5), the 1M / 2M1 ratio depends on the number of impurity phases like eucryptite or sanidine depleting the reaction mixture of Li or Al. There is no solid solution between trilithionite and muscovite; instead, the Li-muscovite crystals consist of domains differing in the relative proportions of muscovite and trilithionite. The overall composition of the synthesised micas which consist of two polytypes can be characterised by 29Si, 1H and 19F MAS NMR spectroscopy. The Si/Al ratio in the tetrahedral layers and thus the content of [4]Al were calculated by analysing the signal intensities of the 29Si MAS NMR experiments. The Li content xest was calculated from the measured tetrahedral Si/Al ratio of the 29Si MAS NMR signals. The calculated Li contents xest of samples between polylithionite and trilithionite agree with the expected values. The F-rich samples show slightly increased values and the OH samples lower values. Lepidolites with only F (x = 1.5 to 2.0, y = 0.0), but not lepidolites with only OH (x = 1.5 to 2.0 and y = 2.0), were observed after synthesis. With decreasing Li content, x≤1.2, Li-muscovites containing mostly hydroxyl (y>1.0) are formed. It was possible to synthesise fluorine containing micas with a Li content as low as 0.3 and y = 0.2 to 1.8. The 19F and 1H MAS NMR experiments reveal that F and OH are not distributed statistically but local structural preferences exist. F is attracted by Li-rich and OH by Al-rich environments. The quadrupolar coupling constant which represents the anisotropy of the Al coordination is low for polylithionite with CQ=1.5 MHz and increases to CQ=3.8 MHz for trilithionite. For tetrahedral Al a smaller increase of CQ from 1.7 to 2.8 MHz is observed. Advancing from trilithionite to muscovite both quadrupolar coupling constants decrease to 2.5 MHz for octahedral and 1.5 MHz for tetrahedral Al. In polylithionite there is the most isotropic environment for octahedral Al; there are only Li2Al sites coordinated by F in the octahedral sheets and O from the tetrahedral sheets which are regular, containing only Si. The distortion and anisotropy for Al in tetrahedral as well as octahedral sheets increases with rising Al content. The most anisotropic environment can be found in trilithionite, especially for octahedral Al.

Pushing the limit of MQMAS for low-γ quadrupolar nuclei in pharmaceutical hydrochlorides

Solid-state NMR of quadrupolar nuclei such as 35Cl has become a useful tool to characterize polymorphism in pharmaceutical hydrochlorides. The two-dimensional multiple-quantum magic-angle spinning (MQMAS) experiment can achieve isotropic resolution, and separate quadrupolar line shapes for samples with multiple sites but the pulse sequence efficiency is often low, limiting applications due to the intrinsically low NMR signals and rf field from the low gyromagnetic ratios γ. The use of cosine low-power MQMAS pulse sequences and high magnetic fields is presented to push the limit of MQMAS for insensitive low-γ quadrupolar nuclei. The improved efficiency and fields up to 35.2 T enable the acquisition of MQMAS spectra for pharmaceutical samples with multiple 35Cl sites, large quadrupolar couplings and/or in diluted dosage forms.

Two- and Three-Dimensional 13C-17O Heteronuclear Correlation NMR Spectroscopy for Studying Organic and Biological Solids.

We report two- and three-dimensional (2D and 3D) 13C-17O heteronuclear correlation solid-state NMR experiments under magic-angle spinning (MAS) conditions. These experiments utilize the D-RINEPT (Dipolar-mediated Refocused Insensitive Nuclei Enhanced by Polarization Transfer) scheme with symmetry-based SR412 recoupling blocks for coherence transfer between 13C and 17O nuclei. First, a 2D 17O → 13C correlation experiment was performed for the [1-13C,17O]-Gly/Gly·HCl cocrystal and [U-13C, 1-17O]-α/β-d-glucose samples. Second, a 2D 17O → 13C MQ-D-RINEPT correlation experiment where the indirect dimension incorporates the multiple-quantum MAS (MQMAS) scheme was tested for obtaining isotropic 17O resolution with [U-13C, 1-17O]-α/β-d-glucose. Third, a new 3D 17O → 13C → 13C correlation experiment was demonstrated where 17O → 13C and 13C → 13C correlations are achieved by D-RINEPT and DARR (Dipolar Assisted Rotational Resonance) sequences, respectively (thus termed as a 3D D-RINEPT/DARR OCC experiment). This new 3D 17O NMR experiment is implemented with the aim for site-resolved solid-state 17O NMR studies.

Isotropic solid-state MQMAS NMR spectra for large quadrupolar interactions using satellite-transition selective inversion pulses and low rf fields

Multiple-quantum magic-angle spinning (MQMAS) pulse sequences are presented that are capable of obtaining isotropic NMR spectra for large quadrupolar interactions using lower rf fields. These experiments rely on rotor period long pulses applied at a large offset from the central-transition, making them selective to the satellite-transitions. Each such pulse gives rise to an anisotropic phase, which can be cancelled to obtain coherent signal evolution if a pair of pulses are applied in a symmetric manner. Thus, efficient excitation and conversion of triple-quantum coherences from and to the central-transition is achieved for MQMAS even for large quadrupolar couplings, by selective inversion of the satellite-transitions using such low-power pulses. Low-power multiple-quantum magic-angle spinning (lpMQMAS) pulse sequences are demonstrated on a model compound, RbNO3, and also applied on β-Ga2O3, a sample with the largest quadrupolar interactions for which isotropic NMR spectra have been obtained to date.

Sensitivity-enhanced multiple-quantum MAS NMR for half-integer spin quadrupolar nuclei using WURST-amplitude shaped pulses

Two-dimensional multiple-quantum MAS (MQMAS) NMR spectroscopy is one of the most widely used solid-state NMR techniques for resolving multiple overlapping central-transition lineshapes for half-integer spin quadrupolar nuclei. In particular when relying on nutation-driven MQ coherence transfers, this technique suffers from low sensitivity that can only be improved by increasing the rf-amplitude of the involved radio-frequency (rf) pulses, which are therefore typically operated at the rf-limit. In such situations, frequently encountered for the three-pulse z-filtered and split-t1 shifted-echo MQMAS NMR sequences, we introduce the advantages of rf-pulses with smoothly truncated amplitude profiles, which we have termed WURST-Amplitude Shaped Pulses (WASPs). When considering the NMR spectrometer hardware, we demonstrate that WASPs feature more suitable properties in comparison to conventional rectangular pulses, enabling a substantial reduction of voltage reflections and transient effects under identical rf-conditions. By employing extensive numerical simulations and experimental validation, we further show that WASPs intrinsically possess a higher potential for nutation-based 3Q excitation involving spin-3/2 and 3Q and 5Q excitation for spin-5/2 quadrupolar nuclei, specifically when large nutation frequencies are available. The concept of smoothly truncating rf-amplitudes is also extended to Fast Amplitude Modulation (FAM) pulses, normally incorporated for rotor-driven 1Q conversion. We additionally evaluate the potential of employing WASPs with peak rf-amplitudes beyond the rf-limit for conventional rectangular rf-pulses.

Simultaneous MQMAS NMR Experiments for Two Half-Integer Quadrupolar Nuclei

A procedure to acquire two Multiple-Quantum Magic Angle Spinning (MQMAS) NMR experiments with the same instrument time is presented. A triply tuned probe is utilized with multiple receivers to collect data with staggered acquisitions and thus more efficiently use the instrument time. The data for one nucleus is collected during the recovery delay of the other nucleus, and vice versa. The instrument time is reduced to 60–80% of the time needed for the single acquisition collection Specifically our approach is presented for recording triple-quantum (3Q) 17O and either 3Q or quintuple-quantum (5Q) 27Al MAS NMR spectra of a 1.18Na2O•5SiO2•Al2O3 glass gel.

A Practical Review of NMR Lineshapes for Spin-1/2 and Quadrupolar Nuclei in Disordered Materials.

NMR is a powerful spectroscopic method that can provide information on the structural disorder in solids, complementing scattering and diffraction techniques. The structural disorder in solids can generate a dispersion of local magnetic and electric fields, resulting in a distribution of isotropic chemical shift δiso and quadrupolar coupling CQ. For spin-1/2 nuclei, the NMR linewidth and shape under high-resolution magic-angle spinning (MAS) reflects the distributions of isotropic chemical shift, providing a rich source of disorder information. For quadrupolar nuclei, the second-order quadrupolar broadening remains present even under MAS. In addition to isotropic chemical shift, structural disorder can impact the electric field gradient (EFG) and consequently the quadrupolar NMR parameters. The distributions of quadrupolar coupling and isotropic chemical shift are superimposed with the second-order quadrupolar broadening, but can be potentially characterized by MQMAS (multiple-quantum magic-angle spinning) spectroscopy. We review analyses of NMR lineshapes in 2D DQ–SQ (double-quantum single-quantum) and MQMAS spectroscopies, to provide a guide for more general lineshape analysis. In addition, methods to enhance the spectral resolution and sensitivity for quadrupolar nuclei are discussed, including NMR pulse techniques and the application of high magnetic fields. The role of magnetic field strength and its impact on the strategy of determining optimum NMR methods for disorder characterization are also discussed.

Structural and chemical heterogeneity in ancient glass probed using gas overcondensation, X-ray tomography, and solid-state NMR

Rare ancient glasses have complex, multi-scale structures requiring more sophisticated and non-destructive pore characterisation techniques than usual. Homotattic patch models for nitrogen adsorption gave better fits to the isotherm data, more accurate void space descriptors, and also greater understanding of the underlying physical factors affecting adsorption, than standard BET. These homotattic patch models revealed the critical role of iron impurities in determining adsorption behaviour. Non-destructive sodium-23 NMR relaxometry validated the homotattic patch model for some natron glasses, and, in turn, was validated using multiple quantum magic-angle spinning (MQMAS) 23Na NMR. X-ray tomography images of the glasses showed the presence of large macroporous bubbles, while FEG-SEM revealed nanopores within the glass matrix. A newly-developed, gas overcondensation technique, suitable for small amounts of low porosity material, assessed the inter-relationship between the disparate levels in this hierarchical porosity. This technique demonstrated that the nanoporosity did not form a ‘corona’ around the bubbles, due to leaching from the glass, as initially supposed from tomography data, but was completely disconnected, and, thus, is probably associated with glass alkalinity. Gas overcondensation is demonstrated as a non-destructive alternative to mercury porosimetry for probing multi-scale porosity in rare artefacts.

Accelerating high-resolution NMR of half-integer quadrupolar nuclei in solids: SPAM-MQMAS and SPAM-STMAS

In solid-state NMR, multiple-quantum MAS (MQMAS) and satellite-transition MAS (STMAS) experiments are well-established techniques to obtain high-resolution spectra of half-integer quadrupolar nuclei. In 2004 and 2005, a soft-pulse-added-mixing (SPAM) concept was introduced by Gan and Amoureux to enhance the S/N ratio of MQMAS and STMAS experiments. Despite their robustness and simplicity, SPAM approaches have not yet been widely applied. Here, we further exploit SPAM concepts for sensitivity enhancement upon acquisition of two-dimensional MQMAS and STMAS spectra and also establish a general procedure upon implementation of SPAM-MQMAS and SPAM-STMAS NMR. Its effectiveness and ease in experimental setup are demonstrated using simulations and experiments performed on I ​= ​3/2 (23Na, 87Rb), 5/2 (27Al, 85Rb) and 9/2 (93Nb) nuclei with a variety of quadrupolar coupling constants (CQ). Compared to the conventional z-filter methods, sensitivity enhancements in between 2 and 4 are achievable with SPAM. We recommend to use SPAM with a ratio of 4:1 for the number of echoes and antiechoes to safely maximize the sensitivity and resolution simultaneously. In addition, a comparison of the experimental approaches is made in the context of SPAM-MQMAS and SPAM-STMAS NMR with respect to repetition delay and spinning frequency, aiming to discuss the precautions upon making a judicious choice of high-resolution NMR methods of half-integer quadrupolar nuclei.

Separation of quadrupolar and paramagnetic shift interactions with TOP-STMAS/MQMAS in solid-state lighting phosphors.

A new approach for processing satellite-transition magic-angle spinning (STMAS) and multiple-quantum magic-angle spinning (MQMAS) data, based on the two-dimensional one-pulse (TOP) method, which separates the second-rank quadrupolar anisotropy and paramagnetic shift interactions via a double shearing transformation, is described. This method is particularly relevant in paramagnetic systems, where substantial inhomogeneous broadening may broaden the lineshapes. Furthermore, it possesses an advantage over the conventional processing of MQMAS and STMAS spectra because it overcomes the limitation on the spectral width in the indirect dimension imposed by rotor synchronization of the sampling interval. This method was applied experimentally to the Al solid-state nuclear magnetic resonance of a series of yttrium aluminum garnets (YAGs) doped with different lanthanide ions, from which the quadrupolar parameters of paramagnetically shifted and bulk unshifted sites were extracted. These parameters were then compared with density functional theory calculations, which permitted a better understanding of the local structure of Ln substituent ions in the YAG lattice.

Structural Role of Phosphate in Metaluminous Sodium Aluminosilicate Glasses As Studied by Solid State NMR Spectroscopy

In this contribution we present a detailed study of the effect of the addition of small to intermediate amounts of P2O5 (up to 7.5 mol %) on the network organization of metaluminous sodium aluminosilicate glasses employing a range of advanced solid state NMR methodologies. The combined results from MAS, MQMAS (multiple quantum MAS), or MAT (magic angle turning) NMR spectroscopy and a variety of dipolar based NMR experiments-27Al{31P}-, 27Al{29Si}-, 29Si{31P}-, and 31P{29Si}-REDOR (rotational echo double resonance) NMR spectroscopy as well as 31P{27Al}- and 29Si{27Al}-REAPDOR (rotational echo adiabatic passage double resonance) NMR-allow for a detailed analysis of the network organization adopted by these glasses. Phosphate is found as QP2, QP3, and QP4 (with the superscript denoting the number of bridging oxygens), the QP4 units can be safely identified with the help of 31P MAT NMR experiments. Al exclusively adopts a 4-fold coordination. The withdrawal of a fraction of the sodium cations from AlO4 units that is needed for charge compensation of the QP2 units necessitates an alternative charge compensation scheme for these AlO4 units via formation of QP4 units or oxygen triclusters. The dipolar NMR experiments suggest a strong preference of P for Al with an average value of ca. 2.4 P-O-Al connections per phosphate tetrahedron. P is thus mainly integrated into the network via P-O-Al bonding, the formation of Si-O-P bonding plays only a minor role.

Solid-state nuclear magnetic resonance investigation of synthetic phlogopite and lepidolite samples.

In the present work, our aim is to decipher the cationic ordering in the octahedral and tetrahedral sheets of two Al-rich synthetic materials, namely, phlogopites of nominal composition K(Mg3-x Alx )[Al1+x Si3-x O10 ](OH)y F2-y and lepidolites in the system trilithionite-polylithionite with composition K (Lix Al3-x )[Al4-2x Si2x O10 ](OH)y F2-y , by directly probing the aluminium distribution through 27 Al and 17 O magic-angle spinning, multiple-quantum magic-angle spinning, and 27 Al-27 Al double-quantum single-quantum nuclear magnetic resonance (NMR) experiments. Notably, 27 Al-27 Al double-quantum single-quantum magic-angle spinning NMR spectra, recorded at 9.34 and/or 20.00 T, show the spatial proximity or avoidance of the Al species inside or between the sheets. In both studied minerals, the ensemble of NMR data suggests a preference for [4] Al in the tetrahedral sheet to occupy position close to the [6] Al of the octahedral sheets.

Sensitivity improvement in 5QMAS NMR experiments using FAM-N pulses

The multiple-quantum magic-angle spinning (MQMAS) experiment is a popular choice for obtaining high-resolution solid-state NMR spectra of quadrupolar nuclei with half-integer spin quantum number. However, its inherently poor sensitivity limits its application in more challenging systems. In particular, the use of higher-order multiple-quantum coherences, which have the potential to provide higher resolution in the isotropic spectrum, results in a further decrease in sensitivity. Here we extend our recent work, which introduced an automated, high-throughput approach to generate amplitude-modulated composite pulses (termed FAM-N) to improve the efficiency of the conversion of three-quantum coherences, and explore the use of similar pulses in five-quantum MAS experiments. We consider three different approaches, and are able to demonstrate that all three provide good enhancements over single pulse conversion in all but the most extreme cases, and work well at a range of spinning rates. We show that FAM-N pulses are robust to variation in the quadrupolar coupling and rf nutation rate, demonstrating their applicability in multisite systems and systems where direct experimental optimisation of complex composite pulses is not feasible. This work will ease the implementation of higher-order MQMAS experiments and enable their application to materials and systems that were previously deemed too difficult to study.

MAS NMR investigations on a metakaolinite-rich brick after zeolitization by alkaline treatments

Abstract A metakaolinite-containing brick made by craftsmen in Central African Republic was treated with sodium hydroxide at 90 °C. After metakaolinite dissolution, gel state Na - aluminosilicates were initially formed and impregnated the surfaces of no-attacked brick grains (mainly sand). This gel changed progressively with time into crystal seeds at remaining brick surfaces. The generation of ‘low silica’ zeolites (NaA and NaP) with molar Si/Al ratios close to 1 was evidenced by the ESEM/EDS technique and their pore size distribution by using N2 adsorption-desorption isotherm at 77 K. 27Al and 29Si MAS NMR spectra of alkali-brick samples were recorded for studying their evolution with NaOH-reagent level and for characterizing newly-generated zeolitic materials in which Si and Al atoms are identified in the classification of alumino-silicates by the coordination number of the central silicon atom and the number of Si and Al second neighbors used. 27Al MQ (multiple quantum) MAS NMR was employed to study the aluminum coordination in synthesized zeolites. 23Na and 1H MAS NMR measurements were performed on alkali brick for evidencing the abundance of hydrated Na+ ions associated with negatively charged brick sites. After checking in the future the ability of zeolitized brick in the removal of heavy metals from wastewaters, this new composite should be of great interest in water treatments at low cost in Central African Republic.

Investigating FAM-N pulses for signal enhancement in MQMAS NMR of quadrupolar nuclei

Although a popular choice for obtaining high-resolution solid-state NMR spectra of quadrupolar nuclei, the inherently low sensitivity of the multiple-quantum magic-angle spinning (MQMAS) experiment has limited its application for nuclei with low receptivity or when the available sample volume is limited. A number of methods have been introduced in the literature to attempt to address this problem. Recently, we have introduced an alternative, automated approach, based on numerical simulations, for generating amplitude-modulated pulses (termed FAM-N pulses) to enhance the efficiency of the triple- to single-quantum conversion step within MQMAS. This results in efficient pulses that can be used without experimental reoptimisation, ensuring that this method is particularly suitable for challenging nuclei and systems. In this work, we investigate the applicability of FAM-N pulses to a wider variety of systems, and their robustness under more challenging experimental conditions. These include experiments performed under fast MAS, nuclei with higher spin quantum numbers, samples with multiple distinct sites, low-γ nuclei and nuclei subject to large quadrupolar interactions.

Solid-State 27Al NMR Spectroscopy of the γ-Al13 Keggin Containing Al Coordinated by a Terminal Hydroxyl Ligand.

We report solid-state 27Al NMR spectroscopic results for the sulfate salt of the γ-Al13 Keggin cluster, γ-[AlO4Al12(OH)25(OH2)11][SO4]3·[H2O]14, that provide a spectroscopic signature for partial hydrolysis of this Keggin-type cluster. In 27Al multiple-quantum magic-angle spinning NMR spectra, all 13 Al positions of the cluster are at least partially resolved and assigned with the aid of density functional theory (DFT) calculations of the 27Al electric field gradients. The isotropic chemical shift of the single tetrahedral site, 75.7 ppm, is nearly identical to that reported for solutions from which the cluster crystallizes. Reflecting broadly similar coordination environments, the octahedral Al show mostly small variations in isotropic chemical shift (+7 to +11 ppm) and quadrupolar coupling constant (CQ; 6-7.5 MHz), except for one resonance that exhibits a much smaller CQ and another site with a larger value. DFT calculations show that deprotonation of a terminal water ligand, to form an η-OH group, causes a large reduction in the 27Al CQ, allowing assignment of a distinct, narrow peak for octahedral Al to this hydroxyl-terminated site. This result suggests a relationship between octahedral 27Al NMR line width and hydrolysis for solids prepared from Keggin-type clusters.

Crystallization of microporous crystals

Zeolites and related microporous crystalline materials have been widely used as ion-exchangers in detergent industry, catalysts in petrochemical and chemical industry, and adsorbents in air separation by pressure swing adsorption. Its crystallization mechanism has been an important issue in zeolite field. Great efforts have been made to understand the events happened in the crystallization process and how the crystallization started. However, a well-accepted conclusion has far been achieved due to the inherent complexity of the synthesis systems and the low resolution of current characterization techniques. This paper briefly reviewed the studies on the crystallization mechanism and crystallization process of microporous crystals. The main points of view on the nucleation and crystal growth were introduced, including “solution-mediated transport mechanism”, “solid hydrogel transformation mechanism”, “dual-phase transition mechanism”, and “generalized mechanism”. In the study of the crystallization of microporous crystals, the identification of the fragments or small structural units is also very important. The typical characterization techniques that can provide such information are briefly introduced, including high resolution chromatography, in situ and ex situ nuclear magnetic resonance (NMR) with newly developed cross polarization (CP), magic angle spinning (MAS), dipolar diphasing, total side-band suppression, multiple-quantum magic-angle spinning (MQMAS), and rotational-echo double resonance (REDOR) methods, electrospray ionization mass spectrography (ESI-MS), and ultraviolet Raman spectra (UV-Raman). Combination of the experimental data and the corresponding calculation can determine the small structural units that cannot be identified by the experimental data only. In the crystallization of microporous crytals, templates or structure-directing agents played an extremely imporant role. In this paper, the diversity of the templates or structure-directing agents was reviewed and the corresponding classification was applied. Finally, a recently developed “reverse temporal evolution” crystallization process was introduced, which might be used to get the structural information of the species finally included into the structure of the resulting open framework at the very early stage of the formation process as well as the structural information of the starting point of the crystallization that a single crystal grew from.

High sensitivity and resolution in 43Ca solid-state NMR experiments

A thorough investigation of solid-state NMR signal enhancement schemes and high-resolution techniques for application to the spin-7/2 43Ca nuclide are presented. Signal enhancement experiments employing double frequency sweeps, hyperbolic secant pulses, and rotor-assisted population transfer, which manipulate the satellite transitions of half-integer quadrupolar nuclei to polarize the central transition (m = + 1/2 ↔ –1/2), are carried out on four well-characterized 43Ca isotopically enriched calcium salts: Ca(NO3)2, Ca(OD)2, CaSO4·2H2O, and Ca(OAc)2·H2O. These results, in conjunction with numerical simulations of 43Ca NMR spectra under magic-angle spinning conditions, are used to identify the technique that provides the most uniform (or quantitative) polarization enhancement as well as the largest signal enhancement factors independent of size of the 43Ca quadrupolar coupling constant, which is the most significant source of resonance broadening in 43Ca NMR spectra. These samples are further investigated using 43Ca double-rotation NMR spectroscopy to yield isotropic, or solution-like, NMR spectra with exquisite resolution. In addition, three unique calcium sites are resolved for the hemihydrated form of calcium acetate (unknown structure), Ca(OAc)2·0.5H2O, with double-rotation NMR, whereas the more common, but more time-consuming, multiple quantum magic-angle spinning technique only clearly resolves two calcium sites. The results shown herein will be useful for other NMR spectroscopists attempting to acquire 43Ca solid-state NMR data for unknown and more complex materials with a higher degree of both sensitivity and resolution.