Recoupled polarization transfer heteronuclear 1H-13C multiple-quantum correlation in solids under ultra-fast MAS.

A new approach for high-resolution solid-state heteronuclear multiple-quantum MAS NMR spectroscopy of dipolar-coupled spin-12 nuclei is introduced. The method is a heteronuclear chemical shift correlation technique of abundant spins, like 1H with rare spins, like 13C in natural abundance. High resolution is provided by ultra-fast MAS and high magnetic fields, high sensitivity being ensured by a direct polarization transfer from the abundant protons to 13C. In a rotor-synchronized variant, the method can be used to probe heteronuclear through-space proximities, while the heteronuclear dipolar coupling constant can quantitatively be determined by measuring multiple-quantum spinning-sideband patterns. By means of recoupling, even weak heteronuclear dipolar interactions are accessible. The capabilities of the technique are demonstrated by measurements on crystalline L-tyrosine hydrochloride salt.     

Kinetics of 1H→13C NMR cross-polarization in polymorphs and solvates of the antipsychotic drug olanzapine

The (1)H→(13)C NMR cross-polarization (CP) was studied under magic-angle spinning at 7.5 kHz in various crystal forms of the antipsychotic drug olanzapine: two polymorphs (metastable I and stable II) and eight solvates containing organic solvent and water molecules. The CP kinetics followed the non-classical I-I(*)-S model, in which CP begins in a spin cluster of proximate abundant spins I(*) and rare spins S, then is controlled by spin diffusion of the abundant spins I from bulk to the I(*) spins of the spin cluster and finally is governed by spin-lattice relaxation of the abundant spins in the rotating frame. The corresponding CP kinetics parameters were determined and analyzed. It was demonstrated that the, λ and T(df) values (the CP time constant, the cluster composition parameter and the (1)H spin-diffusion constant, respectively) were very useful to discriminate the functional groups, especially in the 3D parameter space. In order to conveniently analyze the large amount (175) of the collected CP parameters, the number of the observed variables was reduced using the principal component (PC) analysis. The 2D plot of PC2 vs. PC1 showed adequate separation of the CH(3), CH(2), CH and C cases (C stands for carbons without adjacent hydrogens). It was demonstrated that those cases were located along the PC1 axis in the order of increasing (1)H-(13)C dipolar couplings: C相似文献   

Proton tunneling in a hydrogen bond measured by cross-relaxation field-cycling NMR

A field-cycling NMR pulse sequence is described for studying cross-relaxation between unlike nuclear spins in the solid state. The technique has been applied to study proton tunneling in the hydrogen bonds of a carboxylic acid containing 19F and 1H spins. By studying the B-field dependence of the off-diagonal element of the relaxation matrix that characterizes the longitudinal polarizations, an accurate measure of the proton transfer rate is obtained.     

Heteronuclear X-Y double quantum MAS NMR in crystalline inorganic solids. Applications for indirect detection and spectral editing of rare-spin resonances.

Heteronuclear double quantum MAS NMR experiments in the solid state, involving pairs of highly abundant 31P spins and the rare spins 113Cd, 77Se, and 29Si, are described for the three crystalline compounds CdSiP2, CdGeP2, and Ag7PSe6. These experiments offer the opportunity of indirectly detecting the rare-spin resonance via chemical shift evolution of heteronuclear double quantum coherence. For suitable cases, this method results in significantly enhanced detection sensitivities. Criteria for favorable indirect detection experiments are established. Besides offering high sensitivity, the pulse sequence also acts as a heteronuclear double quantum filter, hence providing heteronuclear correlation and useful spectral editing for peak assignments.     

Improved Spin-Echo-Edited NMR Diffusion Measurements

The need for simple and robust schemes for the analysis of ligand-protein binding has resulted in the development of diffusion-based NMR techniques that can be used to assay binding in protein solutions containing a mixture of several ligands. As a means of gaining spectral selectivity in NMR diffusion measurements, a simple experiment, the gradient modified spin-echo (GOSE), has been developed to reject the resonances of coupled spins and detect only the singlets in the (1)H NMR spectrum. This is accomplished by first using a spin echo to null the resonances of the coupled spins. Following the spin echo, the singlet magnetization is flipped out of the transverse plane and a dephasing gradient is applied to reduce the spectral artifacts resulting from incomplete cancellation of the J-coupled resonances. The resulting modular sequence is combined here with the BPPSTE pulse sequence; however, it could be easily incorporated into any pulse sequence where additional spectral selectivity is desired. Results obtained with the GOSE-BPPSTE pulse sequence are compared with those obtained with the BPPSTE and CPMG-BPPSTE experiments for a mixture containing the ligands resorcinol and tryptophan in a solution of human serum albumin.     

Cyclic and Slice-Selective J Cross Polarization for Heteronuclear Editing and Localized NMR

This work has two objectives. First, heteronuclear editing was considered, with particular aim at proton-detected NMR spectroscopy of rare nuclei. The second aspect refers to localized heteronuclear NMR spectroscopy, implying the editing option. The common basis of both techniques is J cross polarization (or coherent rotating-frame polarization transfer). In the presence of magnetic field gradients this process is slice selective and is introduced as a principle for localized liquid-state NMR, particularly of heteronuclear spins. Heteronuclear editing of NMR lines is performed by the aid of a cyclic cross-polarization pathway. Both methods can be combined to a technique for localized proton-detected NMR spectroscopy of rare nuclei. Test experiments demonstrating the slice selectivity of the transfer process and the efficiency of the cyclic cross-polarization editing procedure are reported. Applications to localized homo- or heteronuclear spectroscopy and imaging are discussed.     

Recoupled Polarization Transfer Heteronuclear H–C Multiple-Quantum Correlation in Solids under Ultra-fast MAS

A new approach for high-resolution solid-state heteronuclear multiple-quantum MAS NMR spectroscopy of dipolar-coupled spin- nuclei is introduced. The method is a heteronuclear chemical shift correlation technique of abundant spins, like ¹H with rare spins, like ¹³C in natural abundance. High resolution is provided by ultra-fast MAS and high magnetic fields, high sensitivity being ensured by a direct polarization transfer from the abundant protons to ¹³C. In a rotor-synchronized variant, the method can be used to probe heteronuclear through-space proximities, while the heteronuclear dipolar coupling constant can quantitatively be determined by measuring multiple-quantum spinning-sideband patterns. By means of recoupling, even weak heteronuclear dipolar interactions are accessible. The capabilities of the technique are demonstrated by measurements on crystalline -tyrosine hydrochloride salt.     

Origin of the NMR signal in liquid water

An experimental method for testing alternative hypotheses about the origin of the NMR signal in liquid water, i.e., whether it is generated by (a) protons 1H with spin 1/2 of H₂O molecules or (b) orthomolecules with spin 1, containing parallel spins and constituting three-quarters of the total number of H₂O molecules, is proposed.     

The NMR line shape of a gas of hydrogen molecules in nanopores

We consider a closed nanopore filled with hydrogen gas in an external magnetic field. Only hydrogen molecules with spin I = 1 contribute to nuclear magnetic resonance (NMR) spin dynamics. Rapid molecular diffusion leads to partial averaging of dipole-dipole interactions (DDI) of spins I = 1 of different molecules. A method for the calculation of the NMR line shape of a hydrogen gas in nanopores is developed. Significant technical difficulties in calculations of the NMR line shape of the system of spins I = 1 coupled by DDI can be overcome with the introduction of a self-interaction with an averaged DDI coupling constant. The accuracy of this procedure is proportional to , where N is the number of hydrogen molecules in the nanocavity. In this approximation the NMR line is Gaussian. The second and fourth moments of the NMR line shape are calculated both from the known line shape and with the Van Vleck theory. They coincide up to the terms of the order of 1/N. The obtained results are in good agreement with experimental data for thin films with ellipsoidal nanopores. The developed theory allows one to extract information about sizes, shapes and orientations of nanopores in solids.     

Analysis of remote detection travel time curves measured from microfluidic channels

Remote detection technique can increase sensitivity of an NMR experiment by several orders of magnitude in microfluidic applications. Travel time experiment is a basic remote detection NMR experiment, which reveals the travel time distribution of the molecules flowing from the encoding coil region to the detector. In this article, we focus on analyzing how flow type (Poiseuille or plug flow), diffusion, dispersion and geometry of the flow channels are manifested in the travel time curves measured from microfluidic channels. We demonstrate that remote detection travel time experiment could be used even as an alternative NMR method for measuring self-diffusion coefficient of a fluid without magnetic field gradients. In addition, we introduce a modified travel time pulse sequence, which removes the signal of unencoded fluid spins as well as the background signal arising from the material inside or close to the detector.     

Indirect NMR detection in solids with multiple cross-polarization periods

The use of indirect detection for signal enhancement in solids is much less common than in liquids, but has attracted renewed interest recently. In this work we describe an indirect detection scheme that offers a large signal enhancement for rare spins in solids. The method uses multiple periods of cross polarization, each followed by an evolution period. The latter is increased stepwise in a pseudo 2D experiment, in which the signal of the rare spin is detected as modulation of the abundant spin. As an illustration of this method, the natural abundance deuterium NMR spectrum of a static powder sample of 1,2,4,5-tetramethylbenzene is presented.     

固体核磁共振魔角旋转条件下的定量交叉极化技术(英文)

交叉极化与魔角旋转结合（CP/MAS）的方法已经成为增强固体核磁共振（NMR）检测灵敏度最重要的技术之一.CP/MAS技术的应用大大提高了固体NMR谱图的采集效率.然而,I-S偶极耦合作用、旋转坐标系下的自旋-晶格弛豫、分子运动,以及样品中丰核的分布情况等因素,通常会导致CP/MAS谱图失去定量作用.近年来,多个研究组通过改进或者设计新型固体NMR脉冲序列,获得了基于CP的可用于定量分析的固体NMR谱图.本综述首先简要介绍了CP及CP动力学,随后介绍了一系列基于CP的定量固体NMR信号增强技术,具体包括ramped-amplitude CP（RAMP-CP）、multiple-contact CP、quantification of CP（QCP）、Lee-Goldburg frequency modulated CP（LG-FMCP）和quantitative CP（QUCP）.     

在CP MAS NMR中测量质子自旋扩散速率的方法

自旋扩散在固体核磁共振的许多现象中都起着非常重要的作用。现有几种理论方案以估算扩散系数。然而在实践中这种估算既不实际也不可靠。本文提出了确定自旋扩散速率的新方案,它利用的是CP MAS NMR中的稀核退极化规律。带质子的稀核磁化矢量在退极化中表现出两个阶段,慢衰减的第二阶段是单一指数过程,它提供了自旋扩散速率的直接度量。自旋扩散实质上是极化转移的一种宏观表现形式,这种转移通过一系列成对自旋的flip-flop进行,可以用一维随机走步模型描述。从退磁过程半对数曲线的斜率可以求得平均flip-flop时间。自旋扩散系数可以由此估算。在一些典型的刚性有机固体和结晶高分子聚合物中,求得平均flip-flop的时间是700微秒左右。它比偶极相关时间大一个数量级。这意味着,自旋扩散时间常数与自旋—自旋弛豫时间常数是很不相同的,虽然这两个相应过程虽密切相关的。由质子线宽估计自旋扩散系数是不可靠的。     

The multiple quantum NMR dynamics in systems of equivalent spins with a dipolar ordered initial state

The multiple quantum (MQ) NMR dynamics in the system of equivalent spins with the dipolar ordered initial state is considered. The high symmetry of the Hamiltonian responsible for the MQ NMR dynamics (the MQ Hamiltonian) is used to develop analytic and numerical methods for the investigation of the MQ NMR dynamics in systems consisting of hundreds of spins from the “first principles.” We obtain the dependence of the intensities of the MQ NMR coherences on their orders (profiles of the MQ NMR coherences) for systems of 200–600 spins. It is shown that these profiles may be well approximated by exponential distribution functions. We also compare the MQ NMR dynamics in the systems of equivalent spins having two different initial states, the dipolar ordered state and the thermal equilibrium state in a strong external magnetic field.     

Multiple Quantum Coherences (MQ) NMR and Entanglement Dynamics in the Mixed-Three-Spin XXX Heisenberg Model with Single-Ion Anisotropy

We analytically investigate Multiple Quantum (MQ) NMR dynamics in a mixed-three-spin (1/2,1,1/2) system with XXX Heisenberg model at the front of an external homogeneous magnetic field B. A single-ion anisotropy property ζ is considered for the spin-1. The intensities dependence of MQ NMR coherences on their orders (zeroth and second orders) for two pairs of spins (1,1/2) and (1/2,1/2) of the favorite tripartite system are obtained. It is also investigated dynamics of the pairwise quantum entanglement for the bipartite (sub)systems (1,1/2) and (1/2,1/2) permanently coupled by, respectively, coupling constants J₁ and J₂, by means of concurrence and fidelity. Then, some straightforward comparisons are done between these quantities and the intensities of MQ NMR coherences and ultimately some interesting results are reported. We also show that the time evolution of MQ coherences based on the reduced density matrix of the pair spins (1,1/2) is closely connected with the dynamics of the pairwise entanglement. Finally, we prove that one can introduce MQ coherence of the zeroth order corresponds to the pair spins (1,1/2) as an entanglement witness at some special time intervals.     

Fast and accurate algorithm for the simulation of NMR spectra of large spin systems

The computational cost for the simulation of NMR spectra grows exponentially with the number of nuclei. Today, the memory available to store the Hamiltonian limits the size of the system that can be studied. Modern computers enable to tackle systems containing up to 13 spins [1], which obviously does not allow to study most molecules of interest in research. This issue can be addressed by identifying groups of spins or fragments that are not or only weakly interacting together, i.e., that only share weakly coupled spin pairs. Such a fragmentation is only permitted in the weak coupling regime, i.e., when the coupling interaction is weak compared to the difference in chemical shift of the coupled spins. Here, we propose a procedure that removes weak coupling interactions in order to split the spin system efficiently and to correct a posteriori for the effect of the neglected couplings. This approach yields accurate spectra when the adequate interactions are removed, i.e., between spins only involved in weak coupling interactions, but fails otherwise. As a result, the computational time for the simulation of 1D spectra grows linearly with the size of the spin system.     

14N NMR作为一种氮含量定量分析的方法及其在检测几种腐殖酸样品中硝酸根离子含量上的应用

本文介绍了氮 1 4核磁共振技术作为一种氮含量定量分析的方法 ,并应用该技术检测了几种腐殖酸样品中硝酸根离子的含量 .结果表明 ,液体氮 1 4核磁共振技术具有较高的灵敏度 ,其定量检测下限可达毫摩尔级 (mmol/L) ,而且操作方便 ,对样品不具损伤性 ,还可以对同一样品中几种小分子氮化物同时进行定量检测 ,是一种较好的氮含量分析方法     

Chemical shift anisotropy edited complete unraveling of overlapped 1H NMR spectra of enantiomers: application to small chiral molecules

The differential values of NMR spectral parameters like chemical shift anisotropies, dipolar couplings and quadrupolar couplings of enantiomers in chiral liquid crystalline media are employed not only for their visualization but also for their quantification. Large differences in chemical shift anisotropies and the quadrupolar couplings between the enantiomers enable the use of 13C and extensive 2H NMR detection for such a purpose. In spite of high magnetic moment, high sensitivity and abundant presence of protons in all the chiral molecules, 1H detection is not routinely employed due to severe overlap of unresolved transitions arising from short and long distance couplings. Furthermore, the doubling of the spectra from two enantiomers and their indistinguishable overlap due to negligible difference in chemical shift anisotropies hampers their discrimination. The present study demonstrates the use of proton chemical shift anisotropy as an exclusive parameter for such a discrimination. The method employs the non-selective excitation of homonuclear Nth quantum coherence of N coupled protons. The simultaneous flipping of all the coupled spins results in a single transition in the multiple quantum dimension at the cumulative sum of their anisotropic chemical shifts for each enantiomer, with the measurable difference between them, resulting in their complete unraveling.     

Natural abundance (17)O NMR spectroscopy of rat brain in vivo

Oxygen is an abundant element that is present in almost all biologically relevant molecules. NMR observation of oxygen has been relatively limited since the NMR-active isotope, oxygen-17, is only present at a 0.037% natural abundance. Furthermore, as a spin 5/2 nucleus oxygen-17 has a moderately strong quadrupole moment which leads to fairly broad resonances (T(2)=1-4 ms). However, the similarly short T(1) relaxation constants allow substantial signal averaging, whereas the large chemical shift range (>300 ppm) improves the spectral resolution of (17)O NMR. Here it is shown that high-quality, natural abundance (17)O NMR spectra can be obtained from rat brain in vivo at 11.74 T. The chemical shifts and line widths of more than 20 oxygen-containing metabolites are established and the sensitivity and potential for (17)O-enriched NMR studies are estimated.