Bruker UK Ltd., Banner Lane, Coventry CV4 9GH, United Kingdom.
TIFR Centre for Interdisciplinary Sciences, Tata Institute of Fundamental Research-Hyderabad, 36/P Gopanpally Village, Ranga Reddy District, Hyderabad 500 046, Telangana, India.
Prog Nucl Magn Reson Spectrosc. 2021 Jun-Aug;124-125:1-56. doi: 10.1016/j.pnmrs.2021.03.001. Epub 2021 Mar 15.
Multiplexing NMR experiments by direct detection of multiple free induction decays (FIDs) in a single experiment offers a dramatic increase in the spectral information content and often yields significant improvement in sensitivity per unit time. Experiments with multi-FID detection have been designed with both homonuclear and multinuclear acquisition, and the advent of multiple receivers on commercial spectrometers opens up new possibilities for recording spectra from different nuclear species in parallel. Here we provide an extensive overview of such techniques, designed for applications in liquid- and solid-state NMR as well as in hyperpolarized samples. A brief overview of multinuclear MRI is also provided, to stimulate cross fertilization of ideas between the two areas of research (NMR and MRI). It is shown how such techniques enable the design of experiments that allow structure elucidation of small molecules from a single measurement. Likewise, in biomolecular NMR experiments multi-FID detection allows complete resonance assignment in proteins. Probes with multiple RF microcoils routed to multiple NMR receivers provide an alternative way of increasing the throughput of modern NMR systems, effectively reducing the cost of NMR analysis and increasing the information content at the same time. Solid-state NMR experiments have also benefited immensely from both parallel and sequential multi-FID detection in a variety of multi-dimensional pulse schemes. We are confident that multi-FID detection will become an essential component of future NMR methodologies, effectively increasing the sensitivity and information content of NMR measurements.
在单次实验中直接检测多个自由感应衰减(FID)来实现多重化 NMR 实验,可以显著增加光谱信息量,并且通常可以提高单位时间内的灵敏度。已经设计了具有同核和多核采集功能的多 FID 检测实验,并且商业光谱仪上的多个接收器的出现为同时从不同核物种记录光谱开辟了新的可能性。在这里,我们提供了此类技术的广泛概述,这些技术专为液体和固态 NMR 以及超极化样品中的应用而设计。还简要概述了多核 MRI,以激发两个研究领域(NMR 和 MRI)之间的思想交叉。结果表明,这些技术如何使设计能够从单个测量中阐明小分子结构的实验。同样,在生物分子 NMR 实验中,多 FID 检测允许在蛋白质中进行完整的共振分配。具有路由到多个 NMR 接收器的多个 RF 微线圈的探头提供了一种增加现代 NMR 系统吞吐量的替代方法,有效地降低了 NMR 分析的成本,同时增加了信息量。在各种多维脉冲方案中,固态 NMR 实验也从并行和顺序多 FID 检测中受益匪浅。我们相信,多 FID 检测将成为未来 NMR 方法学的重要组成部分,有效地提高 NMR 测量的灵敏度和信息量。