EaStCHEM School of Chemistry, University of Edinburgh , David Brewster Rd, Edinburgh EH9 3FJ, U.K.
Anal Chem. 2017 Sep 19;89(18):10013-10021. doi: 10.1021/acs.analchem.7b02437. Epub 2017 Aug 25.
We report a new pure-shift method, termed SHARPER (Sensitive, Homogeneous, And Resolved PEaks in Real time) designed for the analysis of reactions and equilibria by NMR. By focusing on a single selected signal, SHARPER removes all heteronuclear couplings of a selected nucleus without the need to pulse on X channels, thus overcoming hardware limitations of conventional spectrometers. A more versatile decoupling scheme, termed sel-SHARPER, removes all heteronuclear and homonuclear couplings of the selected signal. Both methods are characterized by a periodic inversion of the active spin during the real-time acquisition. In addition to decoupling, they also compensate for pulse imperfections and magnetic field inhomogeneity, generating an extremely narrow singlet with a linewidth approaching limits dictated by the spin-spin relaxation. The decoupling and line narrowing effected by (sel)-SHARPER provide significant increases in the signal-to-noise (S/N) ratio. Increases of 20-fold were routinely achieved for F detection. sel-SHARPER is also applicable to first- and higher-order H spectra. The sensitivity gains are substantially greater for inhomogeneous magnetic fields, including dynamic inhomogeneity caused by gas sparging. The parameters of the pulse sequences have been analyzed in detail to provide guidelines for their most effective application. The considerable reduction in the detection threshold induced by (sel)-SHARPER make the technique particularly suited for in situ monitoring of reaction kinetics. The approach is illustrated by a F NMR study of the protodeboronation of an aryl boronic acid. Here, the high S/N allowed reliable determination of the net protodeoboronation kinetics, and the excess line broadening of F singlets was utilized to characterize the boronic acid/boronate equilibrium kinetics. Oxidation of diphenylphosphine, monitored by P NMR under optimized gas-flow conditions, demonstrated the high tolerance of SHARPER to dynamic inhomogeneity. The principles of the (sel)-SHARPER sequences are expected to find numerous applications in the design of new NMR experiments.
我们报告了一种新的纯位移方法,称为 SHARPER(敏感、均匀、实时分辨峰),用于通过 NMR 分析反应和平衡。通过聚焦于单个选定信号,SHARPER 无需在 X 通道上施加脉冲即可去除所选核的所有异核耦合,从而克服了传统光谱仪的硬件限制。一种更通用的去耦方案,称为 sel-SHARPER,去除所选信号的所有异核和同核耦合。这两种方法的特点是在实时采集过程中,主动自旋周期性反转。除去耦外,它们还补偿了脉冲不完美和磁场不均匀性,生成了一个极其狭窄的单峰,其线宽接近由自旋-自旋弛豫决定的极限。(sel)-SHARPER 产生的去耦和线宽变窄可显著提高信噪比(S/N)。对于 F 检测,通常可实现 20 倍的信号增益。sel-SHARPER 也适用于一阶和更高阶 H 谱。对于不均匀磁场,包括由气体喷射引起的动态不均匀性,灵敏度增益更大。已详细分析了脉冲序列的参数,以提供其最有效应用的指南。(sel)-SHARPER 引起的检测阈值的大幅降低使得该技术特别适合原位监测反应动力学。该方法通过芳基硼酸的原脱硼反应的 F NMR 研究得到了说明。在这里,高 S/N 允许可靠地确定净原脱硼动力学,并且 F 单峰的过剩线宽用于表征硼酸/硼酸盐平衡动力学。在优化的气流条件下通过 P NMR 监测的二苯基膦氧化,证明了 SHARPER 对动态不均匀性的高容忍度。(sel)-SHARPER 序列的原理有望在新的 NMR 实验设计中得到广泛应用。