Equbal Asif, Basse Kristoffer, Nielsen Niels Chr
Center for Insoluble Protein Structures (inSPIN), Interdisciplinary Nanoscience Center (iNANO) and Department of Chemistry, Aarhus University, Gustav Wieds Vej 14, DK-8000 Aarhus C, Denmark.
Phys Chem Chem Phys. 2016 Dec 7;18(45):30990-30997. doi: 10.1039/c6cp06574k. Epub 2016 Nov 2.
We present heteronuclear F refocused CW (rCW) decoupling pulse sequences for solid-state magic-angle-spinning NMR applications. The decoupling sequences have been designed specifically to ensure suppression of the pertinent C-F dipolar coupling interactions while simultaneously suppressing strong anisotropic chemical shift as well as homonuclear F-F dipolar coupling effects as typically present in perfluorated compounds. In an extensive numerical and experimental analysis using a rigid, organic solid as a model compound, it becomes evident that the supercycled rCW schemes markedly improve the decoupling efficiency, leading to substantial enhancements in resolution and sensitivity when compared to previous state-of-the-art methods. Furthermore, considerable gains in robustness toward rf mismatch as well as offset in the radio-frequency carrier frequency are observed, all of which clearly render the new rCW schemes the methods of choice for F decoupling in rigid, fluorinated compounds - which is further supported by a Floquet-based theoretical analysis.
我们提出了用于固态魔角旋转核磁共振应用的异核F重聚焦连续波(rCW)去耦脉冲序列。这些去耦序列经过专门设计,以确保抑制相关的C-F偶极耦合相互作用,同时抑制强各向异性化学位移以及全氟化合物中通常存在的同核F-F偶极耦合效应。在使用刚性有机固体作为模型化合物的广泛数值和实验分析中,很明显超循环rCW方案显著提高了去耦效率,与之前的先进方法相比,分辨率和灵敏度有了大幅提高。此外,还观察到对射频失配以及射频载波频率偏移的鲁棒性有了显著提高,所有这些都清楚地表明新的rCW方案是刚性氟化化合物中F去耦的首选方法——基于弗洛凯理论的分析进一步支持了这一点。