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利用固体中剩余偶极分裂的氮-14核磁共振光谱学。

Nitrogen-14 NMR spectroscopy using residual dipolar splittings in solids.

作者信息

Cavadini Simone, Lupulescu Adonis, Antonijevic Sasa, Bodenhausen Geoffrey

机构信息

Laboratoire de Résonance Magnétique Biomoléculaire, Ecole Polytechnique Fédérale de Lausanne, Batochime, CH-1015 Lausanne, Switzerland.

出版信息

J Am Chem Soc. 2006 Jun 21;128(24):7706-7. doi: 10.1021/ja0618898.

Abstract

It is shown that nuclear magnetic resonance (NMR) spectra of nitrogen-14 (spin I = 1) can be obtained by indirect detection in powders spinning at the magic angle (MAS). The method relies on the transfer of coherence from a neighboring nucleus with S = 1/2, such as carbon-13, to single- or double-quantum transitions of nitrogen-14 nuclei. The transfer of coherence occurs through second-order quadrupole-dipole cross terms, also known as residual dipolar splittings. The two-dimensional NMR spectra reveal powder patterns determined by the second-order quadrupolar interactions of nitrogen-14. Analysis of the spectra yields the quadrupolar coupling constant, CQ, and asymmetry parameter, etaQ, of nitrogen-14. These parameters can be related to the structure of nitrogen-containing solids.

摘要

结果表明,通过在魔角旋转(MAS)的粉末中进行间接检测,可以获得氮-14(自旋I = 1)的核磁共振(NMR)谱。该方法依赖于相干性从相邻的自旋S = 1/2的核(如碳-13)转移到氮-14核的单量子或双量子跃迁。相干性的转移通过二阶四极-偶极交叉项发生,也称为残余偶极分裂。二维NMR谱揭示了由氮-14的二阶四极相互作用决定的粉末图谱。对谱的分析得出氮-14的四极耦合常数CQ和不对称参数etaQ。这些参数可以与含氮固体的结构相关联。

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