14N NMR of magnetically oriented microcrystals.

14N NMR of magnetically oriented microcrystals is reported. With a home-built 1H-13C-14N probe capable of modulating the rotation of the sample around the axis normal to the magnetic field, magnetically oriented microcrystal suspension (MOMS) of l-alanine is made. 14N NMR spectra acquired with various timings during intermittent rotation lead to a rotation pattern of the MOMS similar to that of a single crystal. The effect of orientational distribution of the microcrystals to broadening of the resonance line is discussed.

Double nutation cross-polarization between heteronuclear spins in solids.

We study transfer of magnetization from one nuclear spin species to another in solid-state nuclear magnetic resonance by cross-polarization (CP) employing radiofrequency irradiation that causes simultaneous nutations around a pair of orthogonal axes. Under such DOuble NUTation (DONUT), polarization transfer proceeds in an unexplored arena of what we refer to as the nutation frame, which represents the interaction frame with respect to the Hamiltonian that drives nutation. The effect of DONUT is to develop either the zero-quantum or double-quantum secular component of the heteronuclear dipolar interaction, causing flip-flop or flop-flop exchange of the spin states. We demonstrate DONUT CP in polycrystalline adamantane, glycine, and histidine, also examining folding of the CP spectrum under magic-angle spinning as well as the buildup behavior of the magnetization in comparison with the conventional CP scheme. In addition, we put forth a concept of spin relaxation in the nutation frame, which is a straightforward extension of the well-known concept of spin relaxation in the rotating frame.

Triplet-DNP in magnetically oriented microcrystal arrays.

We explore dynamic nuclear polarization using electron spins in the photo-excited triplet state (Triplet-DNP) in magnetically oriented microcrystal arrays (MOMAs) of pentacene-doped p-terphenyl, in which the individual crystallites are magnetically aligned and UV-cured. In contrast to the conventional approach to Triplet-DNP in powder, which suffers from reduced nuclear polarization due to the averaged electron polarization and the broadening of electron-spin resonance, Triplet-DNP of the MOMAs offers as high dynamic polarization as that attainable in single-crystals. In the case of pentacene-doped p-terphenyl, the enhanced 1H polarization in the one-dimensional MOMA, prepared simply by leaving the suspension in a stationary magnetic field before UV curation, can be higher than that attainable in the powder sample by an order of magnitude and comparable to that in single crystals and in the three-dimensional MOMA made using a modulational rotating field. Triplet-DNP of the MOMAs may find potential applications, such as the polarization of the co-doped target molecules and dissolution experiments.

Crystal-size effect on the kinetics of CO2 adsorption in metal organic frameworks studied by NMR.

We study the dynamics and the exchange of carbon dioxide (CO2) adsorbed in a metal organic framework (MOF) by 13C NMR for various sizes of the host crystal ranging from micrometers to millimeters. We found that the guest CO2 molecules adsorbed in [Zn2(1,4-NDC)2(dabco)]n MOF undergo exchange at a rate that depends on the size of the host crystal, revealing that the smaller the host crystals are, the faster the exchange becomes. Such a trend can be explained by the size-dependent surface-to-volume ratio.

An electro-mechano-optical NMR probe for 1H-13C double resonance in a superconducting magnet.

Electro-mechano-optical (EMO) NMR, an emerging NMR detection technique with signal upconversion from radiofrequency to optical regimes via a Si3N4 nanomembrane, has become compatible with NMR analysis in chemistry using a highly homogeneous but space-limited magnetic field provided by a superconducting magnet (SCM) by development of a compact EMO NMR probe operational inside the SCM bore. Optical 13C NMR signal detection following 1H-13C magnetization transfer in liquid benzene is demonstrated.

Room-temperature hyperpolarization of polycrystalline samples with optically polarized triplet electrons: pentacene or nitrogen-vacancy center in diamond?

We demonstrate room-temperature 13C hyperpolarization by dynamic nuclear polarization (DNP) using optically polarized triplet electron spins in two polycrystalline systems: pentacene-doped [carboxyl-13C] benzoic acid and microdiamonds containing nitrogen-vacancy (NV-) centers. For both samples, the integrated solid effect (ISE) is used to polarize the 13C spin system in magnetic fields of 350-400 mT. In the benzoic acid sample, the 13C spin polarization is enhanced by up to 0.12 % through direct electron-to-13C polarization transfer without performing dynamic 1H polarization followed by 1H-13C cross-polarization. In addition, the ISE has been successfully applied to polarize naturally abundant 13C spins in a microdiamond sample to 0.01 %. To characterize the buildup of the 13C polarization, we discuss the efficiencies of direct polarization transfer between the electron and 13C spins as well as that of 13C-13C spin diffusion, examining various parameters which are beneficial or detrimental for successful bulk dynamic 13C polarization.

Rapid survey of nuclear quadrupole resonance by broadband excitation with comb modulation and dual-mode acquisition.

Nuclear Quadrupole Resonance (NQR) provides spectra carrying information as to the electric-field gradient around nuclei with a spin quantum number I > 1/2 and offers helpful clues toward characterizing the electronic structure of materials of chemical interest. A major challenge in NQR is finding hitherto unknown resonance frequencies, which can scatter over a wide range, requiring time consuming repetitive measurements with stepwise frequency increments. Here, we report on an efficient, two-step NQR protocol by bringing rapid-scan and frequency-comb together. In the first step, wideband excitation and simultaneous signal acquisition, both realized by a non-adiabatic, frequency-swept hyperbolic secant (HS) pulse with comb modulation, offers a clue for the existence/absence of the resonance within the frequency region under investigation. When and only when the sign of the resonance has been detected, the second step is implemented to compensate the limited detection bandwidth of the first and to unambiguously determine the NQR frequency. We also study the spin dynamics under the comb-modulated HS pulse by numerical simulations, and experimentally demonstrate the feasibility of the proposed scheme, which is referred to as RApid-Scan with GApped excitation with Dual-mode Operation (RASGADO) NQR.

In situ solid-state NMR of a magnetically oriented microcrystal suspension.

In situ solid-state NMR measurements of a magnetically oriented microcrystal suspension (MOMS) were demonstrated. Under modulated rotation of the static field, or equivalently, of the sample tube, randomly oriented microcrystals in a viscous liquid medium feel a torque arising from the anisotropic bulk susceptibility and eventually aligned in the same direction. In this way, a three-dimensional MOMS (3D-MOMS) was obtained. To apply an elliptically rotating magnetic field to microcrystals in suspension, a probe to rotate the sample tube around an axis perpendicular to the static magnetic field was developed. Single-crystal (SC) rotation patterns were obtained from the 3D-MOMS by solid-state CP measurements triggered in synchronous with the sample-tube rotation. Unlike the traditional SC method, the 3D-MOMS approach presented here does not require the elaborate adjustment of the direction of the reference frame. The process of three-dimensional magnetic alignment was also studied by monitoring the spectral changes during continuous application of the modulated sample rotation.

Studies on NMR-signal up-conversion from radio-frequency to optical regimes using a lightweight nanomembrane transducer.

Our recent report on Electro-Mechano-Optical (EMO) NMR proved the feasibility of up-conversion of NMR signals from radio-frequency to optical regimes using a metal-coated, high-Q membrane oscillator (Takeda et al., 2018). However, the signal-to-noise ratio, which can in principle exceed that of the conventional electrical detection scheme, was far below than ideal. Here, we developed an aluminum-coated membrane oscillator and used for a capacitor electrode as well as a mirror of an optical cavity. Compared to the gold-deposited membrane used in our previous study, the characteristic frequency of membrane oscillation was significantly higher due to mass reduction, leading to remarkable elimination of noise in the process of conversion of radio-frequency signals to the mechanical oscillation of the membrane. Taking advantage of the significantly improved EMO NMR, we explore physics behind it in terms of coherent transduction of electrical nuclear induction signals to mechanical and then to optical signals. In addition, we study the transient response of the membrane oscillator to electrical excitation due to nuclear induction.

Inner-product NMR spectroscopy: A variant of covariance NMR spectroscopy.

We propose a variant of covariance NMR spectroscopy, namely, inner-product NMR spectroscopy, originally suggested in Takeda (2015). The mathematical operation of inner-product NMR is the same as that of covariance NMR, except that subtraction of the average value of the variable is intentionally omitted, so that the correspondence of the spectrum with that of conventional two-dimensional Fourier-transformation is established without having to request the average to become vanishingly small. We demonstrate inner-product NMR for 13C DARR correlation experiments in a polycrystalline sample of 13C-labeled l-alanine. In covariance, we show that the mixing-time dependence of the peaks is influenced considerably by the choice of the carrier frequency and thereby the center of the spectrum, whereas the inner-product approach is free from such an undesirable effect, while keeping the merit of the covariance NMR.

Determination of nuclear quadrupolar parameters using singularities in field-swept NMR patterns.

We propose a simple data-analysis scheme to determine the coupling constant and the asymmetry parameter of nuclear quadrupolar interactions in field-swept nuclear magnetic resonance (NMR) for static powder samples. This approach correlates the quadrupolar parameters to the positions of the singularities, which can readily be found out as sharp peaks in the field-swept pattern. Moreover, the parameters can be determined without quantitative acquisition and elaborate calculation of the overall profile of the pattern. Since both experimental and computational efforts are significantly reduced, the approach presented in this work will enhance the power of the field-swept NMR for yet unexplored quadrupolar nuclei. We demonstrate this approach in 33S in α-S8 and 35Cl in chloranil. The accuracy of the obtained quadrupolar parameters is also discussed.

Quantification and compensation of the influence of pulse transients on symmetry-based recoupling sequences.

Deviations of amplitude and phase of radio-frequency pulses from the desired values, can have a severe impact on the performance of multiple-pulse sequences in NMR spectroscopy. A particular problem are pulse transients that appear every time there is a discontinuity in amplitude or phase. Based on a Floquet description using pulses with arbitrarily shaped amplitudes and phases we present a systematic study of the influence of pulse transients on symmetry-based pulse sequences in solid-state NMR under magic-angle spinning. This treatment explains the dependence of the experimentally observed transfer efficiency on the details of experimental setups. In addition, three approaches are compared which have the aim to re-establish highly efficient recoupling. We demonstrate that the application of transient-compensated pulses as basic elements of symmetry-based sequences leads to a significantly improved robustness of the experiments with respect to variations in the experimental setup.

Compensating Pulse Imperfections in Solid-State NMR Spectroscopy: A Key to Better Reproducibility and Performance.

The power and versatility of NMR spectroscopy is strongly related to the ability to manipulate NMR interactions by the application of radio-frequency (rf) pulse sequences. Unfortunately, the rf fields seen by the spins differ from the ones programmed by the experimentalist. Pulse transients, i.e., deviations of the amplitude and phase of the rf fields from the desired values, can have a severe impact on the performance of pulse sequences and can lead to inconsistent results. Here, we demonstrate how transient-compensated pulses can greatly improve the efficiency and reproducibility of NMR experiments. The implementation is based on a measurement of the characteristics of the resonance circuit and does not rely on an experimental optimization of the NMR signal. We show how the pulse sequence has to be modified to use it with transient-compensated pulses. The efficiency and reproducibility of the transient-compensated sequence is greatly superior to the original POST-C7 sequence.

Susceptibility cancellation of a microcoil wound with a paramagnetic-liquid-filled copper capillary.

Even though microcoils improve the sensitivity of NMR measurement of tiny samples, magnetic-field inhomogeneity due to the bulk susceptibility effect of the coil material can cause serious resonance-line broadening. Here, we propose to fabricate the microcoil using a thin, hollow copper capillary instead of a wire and fill paramagnetic liquid inside the capillary, so as to cancel the diamagnetic contribution of the copper. Susceptibility cancellation is demonstrated using aqueous solution of NiSO4. In addition, the paramagnetic liquid serves as coolant when it is circulated through the copper capillary, effectively transferring the heat generated by radiofrequency pulses.

Proton decoupling and recoupling under double-nutation irradiation in solid-state NMR.

The effect of (1)H decoupling in magic-angle spinning solid-state NMR is studied under radiofrequency irradiation causing simultaneous nutations around a pair of orthogonal axes. Double-nutation with an arbitrary pair of nutation frequencies is implemented through modulation of the amplitude, phase, and frequency of the transmitting pulses. Similarity and difference of double-nutation decoupling and two-pulse phase-modulation decoupling schemes [A. E. Bennett, C. M. Rienstra, M. Auger, K. V. Lakshmi, and R. G. Griffin, J. Chem. Phys. 103, 6951-6958 (1995) and I. Scholz, P. Hodgkinson, B. H. Meier, and M. Ernst, J. Chem. Phys. 130, 114510 (2009)] are discussed. The structure of recoupling bands caused by interference of the (1)H spin nutation with sample spinning is studied by both experiments and numerical simulations.

Surface functionalization of silica by Si-H activation of hydrosilanes.

Inspired by homogeneous borane catalysts that promote Si-H bond activation, we herein describe an innovative method for surface modification of silica using hydrosilanes as the modification precursor and tris(pentafluorophenyl)borane (B(C6F5)3) as the catalyst. Since the surface modification reaction between surface silanol and hydrosilane is dehydrogenative, progress and termination of the reaction can easily be confirmed by the naked eye. This new metal-free process can be performed at room temperature and requires less than 5 min to complete. Hydrosilanes bearing a range of functional groups, including alcohols and carboxylic acids, have been immobilized by this method. An excellent preservation of delicate functional groups, which are otherwise decomposed in other methods, makes this methodology appealing for versatile applications.

Paramagnetic shimming for wide-range variable-field NMR.

We propose a new passive shimming strategy for variable-field NMR experiments, in which the magnetic field produced by paramagnetic shim pieces placed inside the magnet bore compensates the inhomogeneity of a variable-field magnet for a wide range of magnet currents. Paramagnetic shimming is demonstrated in (7)Li, (87)Rb, and (45)Sc NMR of a liquid solution sample in magnetic fields of 3.4, 4.0, and 5.4T at a fixed carrier frequency of 56.0MHz. Since both the main-field inhomogeneity and the paramagnetic magnetization are proportional to the main-magnet current, the resonance lines are equally narrowed by the improved field homogeneity with an identical configuration of the paramagnetic shim pieces. Paramagnetic shimming presented in this work opens the possibility of high-resolution variable-field NMR experiments.

COMPOZER-based longitudinal cross-polarization via dipolar coupling under MAS.

We propose a cross polarization (CP) sequence effective under magic-angle spinning (MAS) which is tolerant to RF field inhomogeneity and Hartmann-Hahn mismatch. Its key feature is that spin locking is not used, as CP occurs among the longitudinal (Z) magnetizations modulated by the combination of two pulses with the opposite phases. We show that, by changing the phases of the pulse pairs synchronized with MAS, the flip-flop term of the dipolar interaction is restored under MAS.

Recyclable functionalization of silica with alcohols via dehydrogenative addition on hydrogen silsesquioxane.

Synthesis of class II hybrid silica materials requires the formation of covalent linkage between organic moieties and inorganic frameworks. The requirement that organosilylating agents be present to provide the organic part limits the synthesis of functional inorganic oxides, however, due to the water sensitivity and challenges concerning purification of the silylating agents. Synthesis of hybrid materials with stable molecules such as simple alcohols, rather than with these difficult silylating agents, may therefore provide a path to unprecedented functionality. Herein, we report the novel functionalization of silica with organic alcohols for the first time. Instead of using hydrolyzable organosilylating agents, we used stable organic alcohols with a Zn(II) catalyst to modify the surface of a recently discovered highly reactive macro-mesoporous hydrogen silsesquioxane (HSQ, HSiO1.5) monolith, which was then treated with water with the catalyst to form surface-functionalized silica. These materials were comprehensively characterized with FT-IR, Raman, solid-state NMR, fluorescence spectroscopy, thermal analysis, elemental analysis, scanning electron microscopy, and nitrogen adsorption-desorption measurements. The results obtained from these measurements reveal facile immobilization of organic moieties by dehydrogenative addition onto surface silane (Si-H) at room temperature with high loading and good tolerance of functional groups. The organic moieties can also be retrieved from the monoliths for recycling and reuse, which enables cost-effective and ecological use of the introduced catalytic/reactive surface functionality. Preservation of the reactivity of as-immobilized organic alcohols has been confirmed, moreover, by successfully performing copper-catalyzed azide-alkyne cycloaddition (CuAAC) "click" reactions on the immobilized silica surfaces.

Microcoils and microsamples in solid-state NMR.

Recent reports on microcoils are reviewed. The first part of the review includes a discussion of how the geometries of the sample and coil affect the NMR signal intensity. In addition to derivation of the well-known result that the signal intensity increases as the coil size decreases, the prediction that dilution of a small sample with magnetically inert matter leads to better sensitivity if a tiny coil is not available is given. The second part of the review focuses on the issues specific to solid-state NMR. They include realization of magic-angle spinning (MAS) using a microcoil and harnessing of such strong pulses that are feasible only with a microcoil. Two strategies for microcoil MAS, the piggyback method and magic-angle coil spinning (MACS), are reviewed. In addition, MAS of flat, disk-shaped samples is discussed in the context of solid-state NMR of small-volume samples. Strong RF irradiation, which has been exploited in wide-line spectral excitation, multiple-quantum MAS (MQMAS), and dipolar decoupling experiments, has been accompanied by new challenges regarding the Bloch-Siegert effect, the minimum time resolution of the spectrometer, and the time scale of pulse transient effects. For a possible solution to the latter problem, recent reports on active compensation of pulse transients are described.