Dynamic Nuclear Polarization NMR Spectroscopy of Microcrystalline Solids

被引:230
|
作者
Rossini, Aaron J. [1 ]
Zagdoun, Alexandre [1 ]
Hegner, Franziska [1 ]
Schwarzwalder, Martin [2 ]
Gajan, David [1 ]
Coperet, Christophe [2 ]
Lesage, Anne [1 ]
Emsley, Lyndon [1 ]
机构
[1] Univ Lyon CNRS ENS Lyon UCB Lyon 1, Ctr RMN Tres Hauts Champs, F-69100 Villeurbanne, France
[2] ETH, Inorgan Chem Lab, Dept Chem, CH-8093 Zurich, Switzerland
关键词
MODEL ORGANIC-COMPOUNDS; SAMPLE-SPINNING NMR; HIGH-RESOLUTION H-1; STATE NMR; CROSS-POLARIZATION; POWDER CRYSTALLOGRAPHY; HYDROCHLORIDE SALTS; ROTATING SOLIDS; SPECTRA; RELAXATION;
D O I
10.1021/ja308135r
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Dynamic nuclear polarization (DNP) solid-state NMR has been applied to powdered microcrystalline solids to obtain sensitivity enhancements on the order of 100. Glucose, sulfathiazole, and paracetamol were impregnated with bis-nitroxide biradical (bis-cyclohexyl-TEMPO-bisketal, bCTbK) solutions of organic solvents. The organic solvents were carefully chosen to be nonsolvents for the compounds, so that DNP-enhanced solid-state NMR spectra of the unaltered solids could be acquired. A theoretical model is presented that illustrates that for externally doped organic solids characterized by long spin-lattice relaxation times (T-1(H-1) > 200 s), H-1-H-1 spin diffusion can relay enhanced polarization over micrometer length scales yielding substantial DNP enhancements (epsilon). epsilon on the order of 60 are obtained for microcrystalline glucose and sulfathiazole at 9.4 T and with temperatures of ca. 105 K. The large gain in sensitivity enables the rapid acquisition of C-13-C-13 correlation spectra at natural isotopic abundance. It is anticipated that this will be a general method for enhancing the sensitivity of solid-state NMR experiments of organic solids.
引用
收藏
页码:16899 / 16908
页数:10
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