Correlating fast and slow chemical shift spinning sideband patterns in solid-state NMR

被引:29
作者
Orr, RM
Duer, MJ
Ashbrook, SE
机构
[1] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
[2] Univ Cambridge, Dept Earth Sci, Cambridge CB2 3EQ, England
基金
英国工程与自然科学研究理事会;
关键词
solid-state NMR; magic-angle spinning; chemical shift anisotropy; recoupling;
D O I
10.1016/j.jmr.2005.03.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An experiment is presented that enables the measurement of small chemical shift anisotropy tensors under fast magic-angle spinning (MAS). The two-dimensional spectra obtained give a fast MAS sideband pattern in the directly observed dimension with the spinning sideband intensities equivalent to the chemical shift anisotropy scaled by a factor of N, or equivalently the sample spinning frequency scaled by 1/N, in the indirectly observed dimension. The scaling factor may be arbitrarily varied by changing the number and timings of the rotor synchronized pi-pulses used. Desirable features of the experiment include a fixed length pulse sequence and efficient sampling of the indirectly observed dimension. In addition, neither quadrature detection in the indirect dimension nor storage periods are required, consequently no signal intensity is discarded by the pulse sequence. The experiment is demonstrated using P-31 NMR of sodium phosphate and C-13 NMR of fumaric acid monoethyl ester for which a scaling factor of N = 10.2 was employed. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:301 / 309
页数:9
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