Determination of internuclear distances by suppressing spin diffusion in rotating-frame overhauser measurements

1999 ◽  
Vol 17 (2-3) ◽  
pp. 189-196
Author(s):  
S. J. F. Vincent ◽  
G. Bodenhausen
2005 ◽  
Vol 127 (12) ◽  
pp. 4477-4483 ◽  
Author(s):  
Jarrod J. Buffy ◽  
Alan J. Waring ◽  
Mei Hong

2018 ◽  
Vol 4 (6) ◽  
pp. eaat1670 ◽  
Author(s):  
Xinde Tao ◽  
Qi Liu ◽  
Bingfeng Miao ◽  
Rui Yu ◽  
Zheng Feng ◽  
...  

2008 ◽  
pp. 339-343
Author(s):  
Axel Kretschmer ◽  
Robert A. Drake ◽  
Simeon J. Bones ◽  
Michael Neidhoefer ◽  
Manfred Wilhelm ◽  
...  

The combination of cross polarization, dipolar decoupling and magic angle spinning results in liquid-like high-resolution 13 C and 15 N n.m.r. spectra of a wide variety of solid materials. Structural determinations based on such 13 C n.m.r. spectra include the measurement of the extent to which pyrolysed polyacrylonitrile fibres (Orion) retain aliphatic character during the first step of the production of a carbon fibre, the determination of the chemical identity of the cross links formed from an acetyleneterminated polyimide resin, and the characterization of the metabolic products of a bacterial fermentation of wood lignin. All of these non-destructive analyses are performed on intact heterogeneous samples. The high resolution of the carbon experiment can also be exploited by obtaining proton spin-lattice relaxation parameters for chemically different protons in solids. Because of spin diffusion, these parameters are dependent on spatial proximity and so are helpful in measuring the homogeneity of solid blends of polymers such as poly(phenylene oxide) and polystyrene. High-resolution 13 C n.m.r. spectra of polymers can also be used for measuring microscopic chain dynamics. 13 C rotating-frame relaxation parameters observed for polycarbonate and poly (ethylene terephthalate) are related to the effects on motion of annealing, additives and structural substitutions. Individual relaxation rates are observed for individual carbons, so the behaviour of side groups is cleanly separated from that of the main chain. All of the line-narrowing and sensitivity-enhancing techniques applied to 13 C n.m.r. of solids work equally well for 15 N n.m.r. Use of 15 N rotating-frame and cross-polarization parameters leads to the assessment of the relative concentrations of 13 C - 15 N and 12 C - 15 N pair concentrations in the main chains of multiply labelled proteins. Such measurements can be used to characterize the rate of protein turnover in fully expanded soybean leaves, as well as the details of protein synthesis in cultured soybean cotyledons.


2016 ◽  
Vol 49 (42) ◽  
pp. 425104 ◽  
Author(s):  
C Rinaldi ◽  
S Bertoli ◽  
M Asa ◽  
L Baldrati ◽  
C Manzoni ◽  
...  

1999 ◽  
Vol 121 (16) ◽  
pp. 4064-4065 ◽  
Author(s):  
Kaoru Nomura ◽  
K. Takegoshi ◽  
Takehiko Terao ◽  
Kenichi Uchida ◽  
Masatsune Kainosho

Biochemistry ◽  
1994 ◽  
Vol 33 (20) ◽  
pp. 6129-6136 ◽  
Author(s):  
A. E. McDermott ◽  
F. Creuzet ◽  
R. Gebhard ◽  
K. van der Hoef ◽  
M. H. Levitt ◽  
...  

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