Dipolar Recoupling in Magic Angle Spinning Solid-State Nuclear Magnetic Resonance

被引:109
作者
De Paepe, Gael [1 ]
机构
[1] UJF Grenoble 1, UMR E CEA 3, Serv Chim Inorgan & Biol, Inst Nanosci & Cryogenie, F-38054 Grenoble, France
来源
ANNUAL REVIEW OF PHYSICAL CHEMISTRY, VOL 63 | 2012年 / 63卷
关键词
dipolar truncation; polarization transfer; structure determination; solid-state NMR; magic angle spinning; SHIFT CORRELATION SPECTROSCOPY; MOLECULAR TORSIONAL ANGLE; HOMONUCLEAR CORRELATION SPECTROSCOPY; PROTEIN-STRUCTURE DETERMINATION; TILTED ROTATING-FRAME; PROTON-ENHANCED NMR; CHEMICAL-SHIFT; DISTANCE MEASUREMENTS; POLARIZATION TRANSFER; ROTARY RESONANCE;
D O I
10.1146/annurev-physchem-032511-143726
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Solid-state nuclear magnetic resonance (SSNMR) magic angle spinning (MAS) can be used to record high-resolution data dominated by site-specific information. Although MAS introduces high resolution by attenuating the anisotropic broadening, it also suppresses the nuclear dipole-dipole distance information that is the source of most structural data in the spectra. Such information can be reintroduced coherently and thus selectively by the application of a carefully chosen sequence of radiofrequency pulses, an approach that was introduced 20 years ago and is referred to as dipolar recoupling. This review presents the establishment of recoupling techniques in SSNMR and recalls the major steps achieved by the community throughout the last two decades. This review also presents emerging techniques and their corresponding new concepts. Finally, we present some recent developments based on second-order recoupling mechanisms and discuss their implications regarding dipolar truncation and the possibility to extract structural constraints in uniformly labeled systems.
引用
收藏
页码:661 / 684
页数:24
相关论文
共 138 条
[1]  
ABRAGAM A, 1958, CR HEBD ACAD SCI, V246, P2253
[2]  
Abragam A., 1982, NUCL MAGNETISM ORDER
[3]  
Abragam A., 1961, The principles of nuclear magnetism
[4]   RESONANT ROTATIONAL BROADENING OF NUCLEAR MAGNETIC RESONANCE SPECTRA [J].
ANDREW, ER ;
CLOUGH, S ;
FARNELL, LF ;
GLEDHILL, TD ;
ROBERTS, I .
PHYSICS LETTERS, 1966, 21 (05) :505-&
[5]   REMOVAL OF DIPOLAR BROADENING OF NUCLEAR MAGNETIC RESONANCE SPECTRA OF SOLIDS BY SPECIMEN ROTATION [J].
ANDREW, ER ;
BRADBURY, A ;
EADES, RG .
NATURE, 1959, 183 (4678) :1802-1803
[6]   NUCLEAR MAGNETIC RESONANCE SPECTRA FROM A CRYSTAL ROTATED AT HIGH SPEED [J].
ANDREW, ER ;
BRADBURY, A ;
EADES, RG .
NATURE, 1958, 182 (4650) :1659-1659
[7]  
[Anonymous], 1990, Principles of Nuclear Magnetic Resonance in One and Two Dimensions
[8]   2-DIMENSIONAL SPECTROSCOPY - APPLICATION TO NUCLEAR MAGNETIC-RESONANCE [J].
AUE, WP ;
BARTHOLDI, E ;
ERNST, RR .
JOURNAL OF CHEMICAL PHYSICS, 1976, 64 (05) :2229-2246
[9]   TWO-DIMENSIONAL ROTATIONAL SPIN-ECHO NMR IN SOLIDS - RESOLUTION OF ISOTROPIC AND ANISOTROPIC CHEMICAL-SHIFTS [J].
AUE, WP ;
RUBEN, DJ ;
GRIFFIN, RG .
JOURNAL OF MAGNETIC RESONANCE, 1981, 43 (03) :472-477
[10]   HOMONUCLEAR BROAD-BAND DECOUPLING AND 2-DIMENSIONAL J-RESOLVED NMR-SPECTROSCOPY [J].
AUE, WP ;
KARHAN, J ;
ERNST, RR .
JOURNAL OF CHEMICAL PHYSICS, 1976, 64 (10) :4226-4227