Kakita Veera Mohana Rao, Vemulapalli Sahithya Phani Babu, Bharatam Jagadeesh
Centre for NMR and Structural Chemistry, CSIR-Indian Institute of Chemical Technology, Tarnaka, Hyderabad, 500 007, India.
Academy of Scientific and Innovative Research (AcSIR), Hyderabad, 500 007, India.
Magn Reson Chem. 2016 Apr;54(4):308-14. doi: 10.1002/mrc.4376. Epub 2015 Nov 2.
Precise assignments of (1) H atomic sites and establishment of their through-bond COSY or TOCSY connectivity are crucial for molecular structural characterization by using (1) H NMR spectroscopy. However, this exercise is often hampered by signal overlap, primarily because of (1) H-(1) H scalar coupling multiplets, even at typical high magnetic fields. The recent developments in homodecoupling strategies for effectively suppressing the coupling multiplets into nice singlets (pure-shift), particularly, Morris's advanced broadband pure-shift yielded by chirp excitation (PSYCHE) decoupling and ultrahigh resolution PSYCHE-TOCSY schemes, have shown new possibilities for unambiguous structural elucidation of complex organic molecules. The superior broadband PSYCHE-TOCSY exhibits enhanced performance over the earlier TOCSY methods, which however warrants prolonged experimental times due to the requirement of large number of dwell increments along the indirect dimension. Herein, we present fast and band-selective analog of the broadband PSYCHE-TOCSY, which is useful for analyzing complex organic molecules that exhibit characteristic yet crowded spectral regions. The simple pulse scheme relies on band-selective excitation (BSE) followed by PSYCHE homodecoupling in the indirect dimension. The BSE-PSYCHE-TOCSY has been exemplified for Estradiol and a complex carbohydrate mixture comprised of six constituents of closely comparable molecular weights. The experimental times are greatly reduced viz., ~20 fold for Estradiol and ~10 fold for carbohydrate mixture, with respect to the broadband PSYCHE-TOCSY. Furthermore, unlike the earlier homonuclear band-selective decoupling, the BSE-PSYCHE-decoupling provides fully decoupled pure-shift spectra for all the individual chemical sites within the excited band. The BSE-PSYCHE-TOCSY is expected to have significant potential for quick screening of complex organic molecules and mixtures at ultrahigh resolution. Copyright © 2015 John Wiley & Sons, Ltd.
通过¹H NMR光谱对分子结构进行表征时,精确确定¹H原子位点并建立其通过化学键的COSY或TOCSY连接关系至关重要。然而,即使在典型的高磁场下,这项工作也常常受到信号重叠的阻碍,主要原因是¹H-¹H标量耦合多重峰。最近在同核去耦策略方面的进展,能够有效地将耦合多重峰抑制为单一峰(纯位移),特别是通过线性调频脉冲激发产生的Morris高级宽带纯位移(PSYCHE)去耦和超高分辨率PSYCHE-TOCSY方案,为复杂有机分子的明确结构解析展示了新的可能性。先进的宽带PSYCHE-TOCSY相较于早期的TOCSY方法具有更高的性能,然而由于在间接维度上需要大量的驻留增量,其实验时间较长。在此,我们提出了宽带PSYCHE-TOCSY的快速且带选择性类似物,它对于分析具有特征性但光谱区域拥挤的复杂有机分子很有用。简单的脉冲序列依赖于带选择性激发(BSE),随后在间接维度上进行PSYCHE同核去耦。BSE-PSYCHE-TOCSY已在雌二醇和由六种分子量相近的成分组成的复杂碳水化合物混合物中得到验证。相对于宽带PSYCHE-TOCSY,实验时间大幅减少,雌二醇减少了约20倍,碳水化合物混合物减少了约10倍。此外,与早期的同核带选择性去耦不同,BSE-PSYCHE去耦为激发带内的所有单个化学位点提供了完全去耦的纯位移光谱。BSE-PSYCHE-TOCSY有望在超高分辨率下快速筛选复杂有机分子和混合物方面具有巨大潜力。版权所有© 2015 John Wiley & Sons, Ltd.