Estimation of carbon-carbon bond lengths and medium-range internuclear:: Distances by solid-state nuclear magnetic resonance

被引:91
作者
Carravetta, M
Edén, M
Johannessen, OG
Luthman, H
Verdegem, PJE
Lugtenburg, J
Sebald, A
Levitt, MH [1 ]
机构
[1] Univ Stockholm, Div Phys Chem, S-10691 Stockholm, Sweden
[2] Weizmann Inst Sci, Dept Chem Phys, IL-76100 Rehovot, Israel
[3] Numico Res BV, Div Nutr Supplements, NL-6700 CA Wageningen, Netherlands
[4] Leiden Univ, Leiden Inst Chem, NL-2300 RA Leiden, Netherlands
[5] Univ Bayreuth, Bayer Geoinst, D-95440 Bayreuth, Germany
[6] Univ Southampton, Dept Chem, Southampton SO17 1BJ, Hants, England
关键词
D O I
10.1021/ja016027f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We describe magic-angle-spinning NMR methods for the accurate determination of internuclear dipole-dipole. couplings between homonuclear spins-1/2 in the solid state. The new sequences use symmetry principles to treat the effect of magic-angle sample-rotation and resonant radio frequency fields. The pulse-sequence symmetries generate selection rules which reduce the interference of undesirable interactions and improve the robustness of the pulse sequences with respect to chemical shift anisotropies. We show that the pulse sequences may be used to estimate distances between C-13 spins in organic solids, including bond lengths in systems with large chemical shift anisotropies, such as conjugated systems. For bond-length measurements, the precision of the method is +/-2 pm with a systematic overestimate of the internuclear distance by 3 +/-1 pm. The method is expected to be a useful tool for investigating structural changes in macromolecules.
引用
收藏
页码:10628 / 10638
页数:11
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