单扫描快速采样方法及其在NMR中的应用

单扫描快速采样方法利用空间编码技术,只需单次扫描就能获得二维及多维核磁共振(NMR)谱数据,极大地缩短了二维和多维核磁共振谱的采样时间,有望在NMR领域得到广泛的应用. 该文以离散编码单扫描快速采样方法为例阐明了单扫描快速采样方法的原理,介绍了连续幅度调制、连续相位调制等各种单扫描快速采样新方法及其在NMR领域中的应用, 指出了单扫描快速采样方法的局限性,并对其未来发展进行了展望.     

不均匀不稳定磁场下高分辨液体核磁共振新技术的研究进展

高分辨核磁共振（Nuclear Magnetic Resonance,NMR）谱的获得通常需要高度稳定且均匀的强静磁场. 阻抗磁体或阻抗－超导混合磁体可获得比超导磁体高得多的磁场, 但它们的磁场的稳定性与均匀性比较差;另一方面, 在活体定域波谱研究中,样品内部组分的磁化率差异,运动或生理活动等作用将不可避免地导致磁场的不均匀不稳定,并且这些不稳定不均匀性无法通过锁场匀场等传统的方法消除. 基于分子间零量子相干的方法、空间编码单扫描快速方法、反卷积技术等日渐成为在不均匀不稳定磁场下获取高分辨率的NMR谱的研究热点.     

不均匀场下基于分子间双量子相干核磁共振技术的果肉检测

核磁共振（NMR）谱图可在不破坏生物样品的状态下提供组织成分组成及其含量的信息,已被广泛应用于生物、医学和食品检测等领域.NMR谱图分辨率越高,提供的与组织成分相关的信息越丰富、越准确,也越有利于未知成分的定性和定量分析.传统的高分辨NMR谱图通常要在均匀磁场下采集.但在实际应用中,均匀的磁场较难获得.这就使得我们采集的NMR谱图的分辨率,以及由此获得的生物组织成分组成和含量等信息的准确性受到影响.源于远程偶极相互作用的分子间双量子相干（iDQC）技术对磁场均匀度不敏感,可在不均匀场下获得高分辨率NMR谱图.本文采用基于iDQC技术的IDEAL-Ⅱ序列对甲基丙烯酸丁酯、蕃茄和西瓜三种样品进行了NMR实验,结果证明基于iDQC技术在不均匀场下获得水果的高分辨NMR谱图是可行的,这对食品科学以及食品检测具有积极的意义.     

基于哈德曼编码的新型高分辨定域谱

核磁共振（NMR）技术作为一种非植入无损伤的检测技术，已经广泛应用于化学、生物和医学等领域.本文基于哈德曼（Hadamard）编码的分子间单量子相干（iSQC）技术提出了一种新的序列，首先从理论上对该序列进行了简要的分析并阐明其原理，然后用套管模型实验和脑模型实验验证该序列在不均匀磁场下准确定域和快速获取高分辨谱的能力.实验表明，该序列在不均匀磁场下可以快速获取高分辨定域谱，同时抑制溶剂峰信号，具备一定的应用价值.     

基于深度神经网络的时空编码磁共振成像超分辨率重建方法

单扫描时空编码磁共振成像是一种新型超快速磁共振成像技术,它对磁场不均匀和化学位移伪影有较强的抵抗性,但是其固有的空间分辨率较低,因此通常需要进行超分辨率重建,以在不增加采样点数的情况下提高时空编码磁共振图像的空间分辨率.然而,现有的重建方法存在迭代求解时间长、重建结果有混叠伪影残留等问题.为此,本文提出了一种基于深度神经网络的单扫描时空编码磁共振成像超分辨率重建方法.该方法采用模拟样本训练深度神经网络,再利用训练好的网络模型对实际采样信号进行重建.数值模拟、水模和活体鼠脑的实验结果表明,该方法能快速重建出无残留混叠伪影、纹理信息清楚的超分辨率时空编码磁共振图像.适当增加训练样本数量以及在训练样本中加入适当的随机噪声水平,有助于改善重建效果.     

2D NMR技术在石油测井中的应用

近几年,2D NMR技术得到迅速发展,特别是在核磁共振测井领域. 该文将主要介绍2D NMR技术的脉冲序列、弛豫原理以及2D NMR技术在石油测井中应用. 2D NMR技术是在梯度场的作用下,利用一系列回波时间间隔不同的CPMG脉冲进行测量,利用二维的数学反演得到2D NMR. 2D NMR技术可以直接测量自扩散系数、弛豫时间、原油粘度、含油饱和度、可动水饱和度、孔隙度、渗透率等地层流体性质和岩石物性参数. 从2D NMR谱上,可以直观的区分油、气、水,判断储层润湿性,确定内部磁场梯度等. 2D NMR技术为识别流体类型提供了新方法.     

先进固体NMR技术研究高分子结构与动力学

随着固体NMR理论和谱仪硬件技术的不断发展,近年来固体NMR技术在高分子多尺度结构与动力学研究领域中正发挥着越来越重要的作用. 多脉冲及高速魔角旋转（MAS）等质子高分辨技术的发展使得高灵敏度的¹H谱可有效地用于高分子化学结构与链间相互作用的检测;基于化学键（J-耦合）相关和通过空间（偶极耦合）相互作用的各种二维异核相关谱NMR新技术,使得复杂高分子的链结构得以严格解析. 基于MAS下同核和异核偶极-偶极相互作用、化学位移各向异性等各向异性相互作用重聚的系列新技术,使得研究者可在采用高分辨¹H或¹³C 检测信号的同时检测准静态下的各向异性相互作用,进而获得与之密切相关的结构和动力学信息. 通过质子偶极滤波技术可有效检测多相聚合物中的界面相与相区尺寸、高分子共混物中的相容性等问题. 在动力学的研究中,通过质子间自旋扩散的有效压制技术和化学位移各向异性的重聚,目前已经可以有效地获取链段上单个化学键的快速局域运动以及链段的超慢分子运动. 上述丰富的多尺度NMR技术可以使研究者在不同空间和时间尺度上对高分子聚合物的微观结构、相分离和动力学行为等进行详细的研究,进而阐明高分子微观结构与宏观性能的关联. 该文以固体NMR中最主要的2类核（¹H和¹³C）的检测技术为主线,简单介绍近年来固体NMR领域的一些最新研究进展及其在高分子结构和动力学研究中的应用.     

相干衍射成像的相位复原及重建

相干衍射成像是一种对材料体密度敏感的超高分辨成像技术。相较于传统表面敏感的超高分辨成像技术,相干衍射成像利用了硬X射线的强穿透能力,可以深入材料体内部进行成像,且成像分辨能力可以根据成像布局进行调整,最高达到原子级空间分辨能力。这种灵活的空间分辨调整依赖于相干衍射成像独特的相位复原技术,即通过对图像成像强度的过采样,利用含约束的迭代算法同时获得光场的强度及相位,进而对样品进行重建;同时结合图像定向及组合技术,相干衍射成像可以实现对样品的三维重建。本文主要从成像原理、复原算法和重建方法介绍相干衍射成像技术,并结合实验进展及模拟研究展示该技术在多种重建情形下具备的诊断能力,以期较为全面地给出相干衍射成像技术的发展趋势。     

应用半正定规划的目标方位超分辨方法

针对水下目标方位超分辨估计问题,提出了一种基于半正定规划(Sdp)的常规波束(CBF)方位超分辨算法(SdpCBF).Sdp-CBF算法基于常规波束形成获得多目标方位谱数据,利用阵列响应矩阵和半正定规划技术,精确估计目标数量和波达角方向.该算法的本质是利用阵列特性和信号能量信息获得超分辨方位估计,不用进行子空间分解,通过卷积反演的方式将阵列孔径的有限效应消除,在L₂范数约束条件下重构空间谱.仿真表明,Sdp-CBF算法具有较强的噪声抑制能力,对非相干和相干信号均具有目标方位超分辨能力,在低信噪比环境下的方位分辨性能超过多重信号分类(MUSIC)等经典高分辨算法。对消声水池以及湖上实验数据的处理结果显示,Sdp-CBF算法在复杂环境中对相干信号及微弱信号具有较强的分辨能力。      

基于低秩矩阵的非均匀采样NMR波谱重建进展

多维核磁共振（Nuclear Magnetic Resonance，NMR）利用多维波谱来分析分子结构，被广泛用于化学、生物学和医学等领域，但信号采样时间随波谱维度和采样点数增加而迅速增长．非均匀采样通过降低间接维采样点数来加速数据采集，并引入合理的重建方法获得完整的NMR波谱．如何快速重建高质量的波谱，是NMR信号处理研究的前沿．本文主要综述近年来基于低秩矩阵的NMR波谱重建方法的发展．首先介绍了低秩矩阵的相关数学基础；然后从一般低秩矩阵和结构化低秩汉克尔矩阵两个角度来论述重建模型，并讨论相关的NMR波谱应用；最后分析了该技术存在的不足，并展望其未来发展的趋势．     

High-resolution heteronuclear correlation spectroscopy based on spatial encoding and coherence transfer in inhomogeneous fields

Two-dimensional (2D) nuclear magnetic resonance (NMR) spectroscopy has been proven to be a powerful technique for chemical, biological, and medical studies. Heteronuclear single quantum correlation (HSQC) and heteronuclear multiple bond correlation (HMBC) are two frequently used 2D NMR methods. In combination with spatially encoded techniques, a heteronuclear 2D NMR spectrum can be acquired in several seconds and may be applied to monitoring chemical reactions. However, it is difficult to obtain high-resolution NMR spectra in inhomogeneous fields. Inspired by the idea of tracing the difference of precession frequencies between two different spins to yield high-resolution spectra, we propose a method with correlation acquisition option and J-resolved-like acquisition option to ultrafast obtain high-resolution HSQC/HMBC spectra and heteronuclear J-resolved-like spectra in inhomogeneous fields.     

Fast high-resolution nuclear magnetic resonance spectroscopy through indirect zero-quantum coherence detection in inhomogeneous fields

In many cases, high-resolution nuclear magnetic resonance （NMR） spectra are virtually impossible to obtain by con- ventional nuclear magnetic resonance methods because of inhomogeneity of magnetic field and inherent heterogeneity of sample. Although conventional intramolecular zero-quantum coherence （ZQC） can be used to obtain high-resolution spectrum in inhomogeneous field, the acquisition takes rather long time. In this paper, a spatially encoded intramolecular ZQC technique is proposed to fast acquire high-resolution NMR spectrum in inhomogeneous field. For the first time, the gradient-driven decoding technique is employed to selectively acquire intramolecular ZQC signals. Theoretical analyses and experimental observations demonstrate that high-resolution NMR spectral information can be retrieved within several scans even when the field inhomogeneity is severe enough to erase most spectral information. This work provides a new way to enhance the acquisition efficiency of high-resolution intramolecular ZQC spectroscopy in inhomogeneous fields.     

Improving spectral resolution in spatial encoding dimension of single-scan nuclear magnetic resonance 2D spin echo correlated spectroscopy

The spatial encoding technique can be used to accelerate the acquisition of multi-dimensional nuclear magnetic resonance spectra. However, with this technique, we have to make trade-offs between the spectral width and the resolution in the spatial encoding dimension (F1 dimension), resulting in the difficulty of covering large spectral widths while preserving acceptable resolutions for spatial encoding spectra. In this study, a selective shifting method is proposed to overcome the aforementioned drawback. This method is capable of narrowing spectral widths and improving spectral resolutions in spatial encoding dimensions by selectively shifting certain peaks in spectra of the ultrafast version of spin echo correlated spectroscopy (UFSECSY). This method can also serve as a powerful tool to obtain high-resolution correlated spectra in inhomogeneous magnetic fields for its resistance to any inhomogeneity in the F1 dimension inherited from UFSECSY. Theoretical derivations and experiments have been carried out to demonstrate performances of the proposed method. Results show that the spectral width in spatial encoding dimension can be reduced by shortening distances between cross peaks and axial peaks with the proposed method and the expected resolution improvement can be achieved. Finally, the shifting-absent spectrum can be recovered readily by post-processing.     

Ultrafast hetero-nuclear 2D J-resolved spectroscopy

Ultrafast techniques enable the acquisition of 2D NMR spectra in a single scan. In this study, we propose a new ultrafast experiment designed to record hetero-nuclear (1)H-(13)C J-resolved spectra in a fraction of a second. The approach is based on continuous constant-time phase modulated spatial encoding followed by a J-resolved detection scheme. An optional isotopic filter is implemented to remove the signal arising from (1)H bound to (12)C. While the most evident application of the technique proposed in this paper is the direct measurement of one bond scalar (13)C-(1)H couplings for structural elucidation purposes, it also offers interesting potentialities for measuring (13)C isotopic enrichments in metabolic samples. The main features of this methodology are presented, and the analytical performances of the ultrafast hetero-nuclear J-resolved pulse sequence are evaluated on model samples.     

A continuous phase-modulated approach to spatial encoding in ultrafast 2D NMR spectroscopy

Ultrafast 2D NMR replaces the time-domain parametrization usually employed to monitor the indirect-domain spin evolution, with an equivalent encoding along a spatial geometry. When coupled to a gradient-assisted decoding during the acquisition, this enables the collection of complete 2D spectra within a single transient. We have presented elsewhere two strategies for carrying out the spatial encoding underlying ultrafast NMR: a discrete excitation protocol capable of imparting a phase-modulated encoding of the interactions, and a continuous protocol yielding amplitude-modulated signals. The former is general but has associated with it a number of practical complications; the latter is easier to implement but unsuitable for certain 2D NMR acquisitions. The present communication discusses a new protocol that incorporates attractive attributes from both alternatives, imparting a continuous spatial encoding of the interactions yet yielding a phase modulation of the signal. This in turn enables a number of basic experiments that have shown particularly useful in the context of in vivo 2D NMR, including 2D J-resolved and 2D H,H-COSY spectroscopies. It also provides a route to achieving sensitivity-enhanced acquisitions for other homonuclear correlation experiments, such as ultrafast 2D TOCSY. The main features underlying this new spatial encoding protocol are derived, and its potential demonstrated with a series of phase-modulated homonuclear single-scan 2D NMR examples.     

Ultrafast 2D NMR spectroscopy using a continuous spatial encoding of the spin interactions

A new protocol for acquiring multidimensional NMR spectra within a single scan is introduced and illustrated. The approach relies on applying a pair of frequency-chirped excitation and storage pulses in combination with echoing magnetic field gradients, in order to impart the kind of linear spatial encoding of the NMR interactions that is required by ultrafast 2D NMR spectroscopy. It is found that when dealing with 2D NMR experiments involving a t1 amplitude-modulation of the spin evolution, such continuous encoding scheme presents a number of advantages over alternatives employing discrete excitation pulses. From an experimental standpoint this is mainly reflected by the use of a single pair of bipolar gradients during the course of the indirect-domain encoding, as opposed to the numerous (and more intense) gradient echoes required so far. In terms of the spectral outcome, main advantages of the continuous spatial encoding scheme are the avoidance of "ghost peaks" and of "enveloping effects" associated to the discrete excitation mode. The principles underlying this new spatial encoding protocol are derived, and its applicability is demonstrated with homo- and heteronuclear 2D ultrafast NMR applications on small molecule and on protein samples.     

Sensitivity losses and line shape modifications due to molecular diffusion in continuous encoding ultrafast 2D NMR experiments

Recent ultrafast techniques make it possible to obtain multidimensional (nD) NMR spectra in a single scan. These ultrafast methods rely on a spatial encoding process based on radiofrequency (RF) pulses applied simultaneously with magnetic field gradients. Numerous approaches have been proposed in the past few years to perform this excitation process, most of them relying on a continuous excitation of the spins throughout the whole sample. However, the resolution and sensitivity of ultrafast nD spectra are often reduced by molecular diffusion effects due to the presence of gradients during the excitation process. In particular, increasing the excitation period is necessary to improve the resolution in the ultrafast dimension, but it leads to high sensitivity losses due to diffusion. In order to understand better and to limit molecular diffusion effects, a detailed theoretical and experimental study of the various continuous ultrafast excitation processes is carried out in the present study. New numerical simulations of ultrafast echo line shapes are presented and compared to experimental data. The evolution of the signal intensity with the excitation process duration is also simulated and compared to experimental intensity losses. The different excitation schemes are compared in order to determine the best excitation conditions to perform 2D ultrafast experiments with optimum resolution and sensitivity. The experimental and theoretical results put in evidence the efficiency of the multi-echo scheme.