Merging concepts from liquid-state and solid-state NMR spectroscopy for the investigation of supra- and biomolecular systems

被引:14
作者
Schnell, I [1 ]
机构
[1] Max Planck Inst Polymer Res, D-55021 Mainz, Germany
关键词
NMR spectroscopy; fast magic-angle spinning (MAS); high-resolution magic-angle spinning (HRMAS); dipolar recoupling; double-quantum coherences; polarisation transfer;
D O I
10.2174/1573411052948415
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
After the fields of liquid- and solid-state NMR spectroscopy have developed largely independently of each other over the past 50 years, materials of current interest call for new approaches which combine and merge spectroscopic techniques from either side. A particular possibility to promote NMR spectroscopy into this direction is provided by magic-angle sample spinning (MAS), which can be performed either at high speeds in solid-state NMR or at moderate speeds in combination with high-resolution NMR. In this way, new NMR methods and experiments have recently been developed, as will be discussed in this review. In solid-state NMR, new and versatile experiments are based on coherent spin-states and coherent transfer mechanisms, provided that fast MAS ensures efficient averaging of anisotropic interactions, and recoupling schemes selectively re-introduce the interactions of interest. In high-resolution NMR, MAS can be borrowed from solid-state NMR in order to ensure sufficient spectral resolution for samples with residual anisotropies or heterogeneities (so-called HRMAS). In such HRMAS studies, recoupling techniques become applicable and provide fully quantitative information on molecular structure and dynamics.
引用
收藏
页码:3 / 27
页数:25
相关论文
共 137 条
[1]   NUCLEAR MAGNETIC RESONANCE SPECTRA FROM A CRYSTAL ROTATED AT HIGH SPEED [J].
ANDREW, ER ;
BRADBURY, A ;
EADES, RG .
NATURE, 1958, 182 (4650) :1659-1659
[2]   CHEMICAL EFFECTS ON NUCLEAR INDUCTION SIGNALS FROM ORGANIC COMPOUNDS [J].
ARNOLD, JT ;
DHARMATTI, SS ;
PACKARD, ME .
JOURNAL OF CHEMICAL PHYSICS, 1951, 19 (04) :507-507
[3]  
ASHBROOK E, J MAGN RESON, V147, P238
[4]   2-DIMENSIONAL SPECTROSCOPY - APPLICATION TO NUCLEAR MAGNETIC-RESONANCE [J].
AUE, WP ;
BARTHOLDI, E ;
ERNST, RR .
JOURNAL OF CHEMICAL PHYSICS, 1976, 64 (05) :2229-2246
[5]   MULTIPLE-QUANTUM DYNAMICS IN SOLID-STATE NMR [J].
BAUM, J ;
MUNOWITZ, M ;
GARROWAY, AN ;
PINES, A .
JOURNAL OF CHEMICAL PHYSICS, 1985, 83 (05) :2015-2025
[6]   CORRELATION OF PROTON AND N-15 CHEMICAL-SHIFTS BY MULTIPLE QUANTUM NMR [J].
BAX, A ;
GRIFFEY, RH ;
HAWKINS, BL .
JOURNAL OF MAGNETIC RESONANCE, 1983, 55 (02) :301-315
[7]   AN NMR TECHNIQUE FOR TRACING OUT THE CARBON SKELETON OF AN ORGANIC-MOLECULE [J].
BAX, A ;
FREEMAN, R ;
FRENKIEL, TA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1981, 103 (08) :2102-2104
[8]   NATURAL ABUNDANCE C-13-C-13 COUPLING OBSERVED VIA DOUBLE-QUANTUM COHERENCE [J].
BAX, A ;
FREEMAN, R ;
KEMPSELL, SP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1980, 102 (14) :4849-4851
[9]   AN IMPROVED METHOD FOR TWO-DIMENSIONAL HETERONUCLEAR RELAYED-COHERENCE-TRANSFER NMR-SPECTROSCOPY [J].
BAX, A ;
DAVIS, DG ;
SARKAR, SK .
JOURNAL OF MAGNETIC RESONANCE, 1985, 63 (01) :230-234
[10]   HETERONUCLEAR DECOUPLING IN ROTATING SOLIDS [J].
BENNETT, AE ;
RIENSTRA, CM ;
AUGER, M ;
LAKSHMI, KV ;
GRIFFIN, RG .
JOURNAL OF CHEMICAL PHYSICS, 1995, 103 (16) :6951-6958