14N overtone transition in double rotation solid-state NMR

被引:15
|
作者
Haies, Ibraheem M. [1 ,2 ]
Jarvis, James A. [3 ]
Brown, Lynda J. [1 ]
Kuprov, Ilya [1 ]
Williamson, Philip T. F. [3 ]
Carravetta, Marina [1 ]
机构
[1] Univ Southampton, Sch Chem, Southampton SO17 1BJ, Hants, England
[2] Univ Mosul, Dept Chem, Coll Sci, Mosul, Iraq
[3] Univ Southampton, Ctr Biol Sci, Southampton SO17 1BJ, Hants, England
基金
英国工程与自然科学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
NUCLEAR-MAGNETIC-RESONANCE; ANGLE-SPINNING NMR; QUADRUPOLAR NUCLEI; SPECTROSCOPY; SPECTRA; POLARIZATION; C-13;
D O I
10.1039/c5cp03266k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Solid-state NMR transitions involving outer energy levels of the spin-1 N-14 nucleus are immune, to first order in perturbation theory, to the broadening caused by the nuclear quadrupole interaction. The corresponding overtone spectra, when acquired in conjunction with magic-angle sample spinning, result in lines, which are just a few kHz wide, permitting the direct detection of nitrogen compounds without the need for labeling. Despite the success of this technique, "overtone'' resonances are still broadened due to indirect, second order effects arising from the large quadrupolar interaction. Here we demonstrate that another order of magnitude in spectral resolution may be gained by using double rotation. This brings the width of the N-14 solid-state NMR lines much closer to the region commonly associated with high-resolution solid-state NMR spectroscopy of N-15 and demonstrates the improvements in resolution that may be possible through the development of pulsed methodologies to suppress these second order effects.
引用
收藏
页码:23748 / 23753
页数:6
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