Radboud University Nijmegen, Institute for Molecules and Materials, Heyendaalseweg 135, 6525 AJ Nijmegen, The Netherlands.
J Magn Reson. 2013 Jun;231:79-89. doi: 10.1016/j.jmr.2013.03.008. Epub 2013 Mar 29.
The use of fluorine in molecules obtained from chemical synthesis has become increasingly important within the pharmaceutical and agricultural industry. NMR characterization of these compounds is of great value with respect to their structure elucidation, their screening in metabolomics investigations and binding studies. The favorable NMR properties of the fluorine nucleus make NMR with fluorine detection of great value in this respect. A suite of NMR 2D F-F- and F-C-correlation experiments with fluorine detection was applied to the assignment of resonances, (n)J(CF)- and (n)J(FF)-couplings as well as the determination of their size and sign. The utilization of this experiment suite was exemplarily demonstrated for a highly fluorinated vinyl alkyl ether. Especially F-C HSQC and J-scaled F-C HMBC experiments allowed determining the size of the J-couplings of this compound. The relative sign of its homo- and heteronuclear couplings was achieved by different combinations of 2D NMR experiments, including non-selective and F2-selective F-C XLOC, F2-selective F-C HMQC, and F-F COSY. The F2-one/two-site selective F-C XLOC versions were found highly useful, as they led to simplifications of the common E.COSY patterns and resulted in a higher confidence level of the assignment by using selective excitation. The combination of F2-one/two-site selective F-C XLOC experiments with a F2-one-site selective F-C HMQC experiment provided the signs of all (n)J(CF)- and (n)J(FF)-couplings in the vinyl moiety of the test compound. Other combinations of experiments were found useful as well for special purposes when focusing for example on homonuclear couplings a combination of F-F COSY-10 with a F2-one-site selective F-C HMQC could be used. The E.COSY patterns in the spectra demonstrated were analyzed by use of the spin-selective displacement vectors, and in case of the XLOC also by use of the DQ- and ZQ-displacement vectors. The variety of experiments presented shall contribute to facilitate the interpretation of F-C correlations as well as to open alternative pathways for the determination of size and signs of homo- and heteronuclear couplings of multiply fluorinated small molecules.
在制药和农业领域,化学合成分子中氟的使用变得越来越重要。这些化合物的 NMR 特征在结构阐明、代谢组学研究和结合研究中的筛选方面具有重要价值。氟核的有利 NMR 性质使得在这方面使用氟检测 NMR 具有很高的价值。一套带有氟检测的 NMR 2D F-F 和 F-C 相关实验被应用于共振的分配、(n)J(CF)-和(n)J(FF)-偶合以及它们大小和符号的确定。该实验套件的应用实例为高度氟化的乙烯基烷基醚。特别是 F-C HSQC 和 J 标度的 F-C HMBC 实验允许确定该化合物 J 偶合的大小。通过不同的二维 NMR 实验组合,包括非选择性和 F2-选择性 F-C XLOC、F2-选择性 F-C HMQC 和 F-F COSY,实现了同核和异核偶合的相对符号。发现 F2-单/双位点选择性 F-C XLOC 版本非常有用,因为它们简化了常见的 E.COSY 模式,并通过选择性激发提高了分配的置信度水平。F2-单/双位点选择性 F-C XLOC 实验与 F2-单位点选择性 F-C HMQC 实验的组合提供了测试化合物乙烯基部分中所有(n)J(CF)-和(n)J(FF)-偶合的符号。其他实验组合也被发现对于特殊目的有用,例如,当聚焦于同核偶合时,可以使用 F-F COSY-10 与 F2-单位点选择性 F-C HMQC 的组合。所展示的光谱中的 E.COSY 模式通过使用自旋选择性位移向量进行了分析,在 XLOC 的情况下,也通过使用 DQ 和 ZQ 位移向量进行了分析。所呈现的实验多样性将有助于促进 F-C 相关的解释,并为确定多氟小分子同核和异核偶合的大小和符号开辟替代途径。