Pure shift NMR approach for fast and accurate extraction of heteronuclear couplings

被引:18
作者
Chaudhari, Sachin Rama [1 ]
Suryaprakash, N. [1 ]
机构
[1] Indian Inst Sci, Solid State & Struct Chem Unit, NMR Res Ctr, Bangalore 560012, Karnataka, India
关键词
RELATIVE SIGNS; CONSTANTS; SPECTROSCOPY; SCALAR; DEPENDENCE; FLUORINE; CONFIGURATION; ELUCIDATION; SPECTRA; BOND;
D O I
10.1039/c4ra01436g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The direct and accurate determination of heteronuclear ((n)J(HX), X = F-19, P-31) couplings from the one dimensional H-1-NMR spectrum is severely hampered due to the simultaneous presence of large numbers of (n)J(HH). The present study demonstrates the utility of the pure shift NMR approach for spectral simplification, and precise and direct measurement of heteronuclear couplings. As a consequence of refocusing of homonuclear couplings ((n)J(HH)) by the pure shift NMR, only heteronuclear couplings ((n)J(HX)) appear as simple multiplets at the resonance position of each chemically non-equivalent proton, enabling their direct measurement from the 1D-H-1 spectrum. The experiment is demonstrated on a number of molecules containing either F-19 or P-31, where (n)J(HF) and (n)J(HP) could be precisely measured in a straightforward manner. The distinct advantage of the experiment is demonstrated on molecules containing more than one fluorine atom, where most of the available NMR experiments fail or have restricted utility.
引用
收藏
页码:15018 / 15021
页数:4
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