Combining solid-state NMR spectroscopy with first-principles calculations – a guide to NMR crystallography

The authors would like to thank the ERC (EU FP7 Consolidator Grant 614290 “EXONMR”) and SEA would like to thank the Royal Society and the Wolfson Foundation for a merit award, and the RSC for the award of the 2015 Corday Morgan Prize.Recent advances in the application of first-principles calculations of NMR parameters to periodic systems have resulted in widespread interest in their use to support experimental measurement. Such calculations often play an important role in the emerging field of “NMR crystallography”, where NMR spectroscopy is combined with techniques such as diffraction, to aid structure determination. Here, we discuss the current state-of-the-art for combining experiment and calculation in NMR spectroscopy, considering the basic theory behind the computational approaches and their practical application. We consider the issues associated with geometry optimisation and how the effects of temperature may be included in the calculation. The automated prediction of structural candidates and the treatment of disordered and dynamic solids are discussed. Finally, we consider the areas where further development is needed in this field and its potential future impact.Publisher PDFPeer reviewe

Calculating NMR parameters in aluminophosphates : evaluation of dispersion correction schemes

Periodic density functional theory (DFT) calculations have recently emerged as a popular tool for assigning solid-state nuclear magnetic resonance (NMR) spectra. However, in order for the calculations to yield accurate results, accurate structural models are also required. In many cases the structural model (often derived from crystallographic diffraction) must be optimised (i.e., to an energy minimum) using DFT prior to the calculation of NMR parameters. However, DFT does not reproduce weak long-range "dispersion'' interactions well, and optimisation using some functionals can expand the crystallographic unit cell, particularly when dispersion interactions are important in defining the structure. Recently, dispersion-corrected DFT (DFT-D) has been extended to periodic calculations, to compensate for these missing interactions. Here, we investigate whether dispersion corrections are important for aluminophosphate zeolites (AlPOs) by comparing the structures optimised by DFT and DFT-D (using the PBE functional). For as-made AlPOs (containing cationic structure-directing agents (SDAs) and framework-bound anions) dispersion interactions appear to be important, with significant changes between the DFT and DFT-D unit cells. However, for calcined AlPOs, where the SDA-anion pairs are removed, dispersion interactions appear much less important, and the DFT and DFT-D unit cells are similar. We show that, while the different optimisation strategies yield similar calculated NMR parameters (providing that the atomic positions are optimised), the DFT-D optimisations provide structures in better agreement with the experimental diffraction measurements. Therefore, it appears that DFT-D calculations can, and should, be used for the optimisation of calcined and as-made AlPOs, in order to provide the closest agreement with all experimental measurements.PostprintPeer reviewe

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

The authors would like to thank EPSRC (EP/K503162/1) for the award of a studentship to HFC and the ERC (EU FP7 Consolidator Grant 614290 “EXONMR”) for support. SEA would also like to thank the Royal Society and Wolfson Foundation for a merit award. The UK 850 MHz solid-state NMR Facility used in this research was funded by EPSRC and BBSRC (contract reference PR140003), as well as the University of Warwick including via part funding through Birmingham Science City Advanced Materials Projects 1 and 2 supported by Advantage West Midlands (AWM) and the European Regional Development Fund (ERDF). Financial support from the TGIR-RMN-THC Fr3050 CNRS to access the 800 MHz spectrometer (Lille) is gratefully acknowledged.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.Publisher PDFPeer reviewe

Solid-state NMR spectroscopy

M.H. acknowledges support by National Institutes of Health (NIH) grant GM066976.Solid-state nuclear magnetic resonance (NMR) spectroscopy is an atomic-level method used to determine the chemical structure, three-dimensional structure, and dynamics of solids and semi-solids. This Primer summarizes the basic principles of NMR as applied to the wide range of solid systems. The fundamental nuclear spin interactions and the effects of magnetic fields and radiofrequency pulses on nuclear spins are the same as in liquid-state NMR. However, because of the anisotropy of the interactions in the solid state, the majority of high-resolution solid-state NMR spectra is measured under magic-angle spinning (MAS), which has profound effects on the types of radiofrequency pulse sequences required to extract structural and dynamical information. We describe the most common MAS NMR experiments and data analysis approaches for investigating biological macromolecules, organic materials, and inorganic solids. Continuing development of sensitivity-enhancement approaches, including 1H-detected fast MAS experiments, dynamic nuclear polarization, and experiments tailored to ultrahigh magnetic fields, is described. We highlight recent applications of solid-state NMR to biological and materials chemistry. The Primer ends with a discussion of current limitations of NMR to study solids, and points to future avenues of development to further enhance the capabilities of this sophisticated spectroscopy for new applications.PostprintPeer reviewe

Understanding the synthesis and reactivity of ADORable zeolites using NMR spectroscopy

The authors would like to thank the ERC (EU FP7 Consolidator Grant 614290 EXONMR and Advanced Grant 787073 ADOR) and EPSRC (EP/N509759/1) for a studentship for CMR. The research data (and/or materials) supporting this publication can be accessed at https://doi.org/10.17630/d82e58e4-b4a0-40b3-8156-5cbf80eeea72Zeolites remain one of the most important class of industrial catalyst used today, and with the urgent drive for transition from petrochemical to renewable feedstocks there is a renewed interest in developing new types of zeolite. Recent synthetic advances in the field have included the development of the Assembly-Disassembly-Organisation-Reassembly (ADOR) method. In this short review we will discuss how solid-state NMR experiments can be used to probe the mechanism of the process by characterising the structure of the intermediates and products, show how 17O NMR spectroscopy can be used to probe the reactivity of ADORable zeolites and explain how this in turn can lead to fundamental questions of how zeolites behave in the presence of liquid water.Publisher PDFPeer reviewe

Exploring cation distribution in ion-exchanged Al,Ga-containing metal-organic frameworks using 17O NMR spectroscopy

The authors would like to thank the ERC (Advanced Grant 787073 ADOR) for support. The UK High-Field Solid-State NMR Facility used in this research was funded by EPSRC and BBSRC (EP/T015063/1), in addition to (for results at 850 MHz) he University of Warwick including via part funding through Birmingham Science City Advanced Materials Projects 1 and 2 supported by Advantage West Midlands (AWM) and the European Regional Development Fund (ERDF), and for the 1 GHz instrument, (EP/R029946/1). Collaborative assistance from the Facility Manager Team (Dr Trent Franks, University of Warwick) is acknowledged. The Jeol JSM-IT200 SEM used in this research was supported by the EPSRC Light Element Analysis Facility Grant (EP/T019298/1) and the EPSRC Strategic Equipment Resource Grant (EP/R023751/1). Collaborative assistance from Dr David Miller (University of St Andrews) is acknowledged.A mixed-metal metal–organic framework, (Al,Ga)-MIL-53, synthesised by post-synthetic ion exchange has been investigated using solid-state nuclear magnetic resonance (NMR) spectroscopy, microscopy and energy dispersive X-ray (EDX) spectroscopy. 17O enrichment during the ion-exchange process enables site specific information on the metal distribution to be obtained. Within this work two ion-exchange processes have been explored. In the first approach (exchange of metals in the framework with dissolved metal salts), 17O NMR spectroscopy reveals the formation of crystallites with a core–shell structure, where the cation exchange takes place on the surface of these materials forming a shell with a roughly equal ratio of Al3+ and Ga3+. For the second approach (exchange of metals between two frameworks), no core–shell structure is observed, and instead crystallites containing a majority of Al3+ are obtained with lower levels of Ga3+. Noticeably, these particles show little variation in the metal cation distribution between crystallites, a result not previously observed for bulk (Al,Ga)-MIL-53 materials. In all cases where ion exchange has taken place NMR spectroscopy reveals a slight preference for clustering of like cations.Publisher PDFPeer reviewe

Ionothermal synthesis and characterization of CoAPO-34 molecular sieve

The cobalt-doped aluminophosphate molecular sieve, CoAPO-34 (with the chabazite-type topology) was prepared under ionothermal conditions using 1-ethyl-3-methylimidazolium bromide (EMIMBr) ionic liquid in presence of 1,6-hexanediamine (HDA). The HDA is not incorporated in CoAPO-34, but is required to mediate the availability of Co2+ during the synthesis. The material was characterized using powder X-ray diffraction (PXRD), thermogravimetric analysis (TGA) and solid-state NMR spectroscopy. Wideline 31P NMR spectroscopy showed broad signals (∼5000–10000 ppm wide), confirming that paramagnetic cobalt ions are successfully incorporated within the framework of the materials.PostprintPeer reviewe

Interior Design Studio; Selection of students’ works in academic year 2014/2015 [ed. Dina Vulin Ileković]

Design of a building or a space always starts and ends with the interior, with thinking and developing a sensitivity towards it. Materials, textures, colours of the planes and volumes correspond to the forms and proportions of the human body while aesthetic experience derives from the psychological complexity of the human mind. This publication shows continuity of a high-quality approach to interior design teaching. It clearly illustrates the way the assignment is conceived and presents the results that students achieved in Interior Design Studio in academic year 2014/15. The twelve most successful projects have been selected here for presentation. The content of this publication is effectively organized and presented thus providing good insight into the course activities

The ambient hydration of the aluminophosphate JDF-2 to AlPO-53(A):insights from NMR crystallography

The aluminophosphate (AlPO) JDF-2 is prepared hydro­thermally with methyl­ammonium hydroxide (MAH+·HO-, MAH+ = CH3NH3+), giving rise to a microporous AEN-type framework with occluded MAH+ cations and extra-framework (Al-bound) HO- anions. Despite the presence of these species within its pores, JDF-2 can hydrate upon exposure to atmospheric moisture to give AlPO-53(A), an isostructural material whose crystal structure contains one mol­ecule of H2O per formula unit. This hydration can be reversed by mild heating (such as the frictional heating from magic angle spinning). Previous work has shown good agreement between the NMR parameters obtained experimentally and those calculated from the (optimized) crystal structure of JDF-2. However, several discrepancies are apparent between the experimental NMR parameters for AlPO-53(A) and those calculated from the (optimized) crystal structure (e.g. four 13C resonances are observed, rather than the expected two). The unexpected resonances appear and disappear reversibly with the respective addition and removal of H2O, so clearly arise from AlPO-53(A). We investigate the ambient hydration of JDF-2 using qu­anti­tative 31P MAS NMR to follow the transformation over the course of 3 months. The structures of JDF-2 and AlPO-53(A) are also investigated using a combination of multinuclear solid-state NMR spectroscopy to characterize the samples, and first-principles density functional theory (DFT) calculations to evaluate a range of possible structural models in terms of calculated NMR parameters and energetics. The published structure of JDF-2 is shown to be a good representation of the dehydrated material, but modification of the published structure of AlPO-53(A) is required to provide calculated NMR parameters that are in better agreement with experiment. This modification includes reorientation of all the MAH+ cations and partial occupancy of the H2O sites

Water in the Earth's mantle: A solid-state NMR study of hydrous wadsleyite

Wadsleyite, β-(Mg,Fe)2SiO4, is the main component of the transition zone in the Earth's mantle, at depths of 410-530 km below the surface. This mineral has received considerable interest as a potential reservoir for the vast amount of hydrogen, as hydro