11B Nuclear Spin–Electron Spin Interactions in 11B MAS NMR Spectra of Paramagnetic Metal Borohydrides

Author(s):  
Jørgen Skibsted ◽  
SeyedHosein Payandeh ◽  
Morten B. Ley ◽  
Torben R. Jensen
1992 ◽  
Vol 96 (19) ◽  
pp. 7560-7567 ◽  
Author(s):  
John V. Hanna ◽  
Mark E. Smith ◽  
S. N. Stuart ◽  
Peter C. Healy

2005 ◽  
Vol 97 (4) ◽  
pp. 043706 ◽  
Author(s):  
Seungwon Lee ◽  
Paul von Allmen ◽  
Fabiano Oyafuso ◽  
Gerhard Klimeck ◽  
K. Birgitta Whaley

2009 ◽  
Vol 36 (2-4) ◽  
pp. 181-194 ◽  
Author(s):  
Elena G. Bagryanskaya ◽  
David Bardelang ◽  
Sandrine Chenesseau ◽  
Jean-Pierre Finet ◽  
Laszlo Jicsinszky ◽  
...  

2009 ◽  
Vol 24 (2) ◽  
pp. 023001 ◽  
Author(s):  
Y Hirayama ◽  
G Yusa ◽  
K Hashimoto ◽  
N Kumada ◽  
T Ota ◽  
...  

2002 ◽  
Vol 80 (5) ◽  
pp. 597-604 ◽  
Author(s):  
S J Opella ◽  
A Nevzorov ◽  
M F Mesleh ◽  
F M Marassi

Current strategies for determining the structures of membrane proteins in lipid environments by NMR spectroscopy rely on the anisotropy of nuclear spin interactions, which are experimentally accessible through experiments performed on weakly and completely aligned samples. Importantly, the anisotropy of nuclear spin interactions results in a mapping of structure to the resonance frequencies and splittings observed in NMR spectra. Distinctive wheel-like patterns are observed in two-dimensional 1H–15N heteronuclear dipolar/15N chemical shift PISEMA (polarization inversion spin-exchange at the magic angle) spectra of helical membrane proteins in highly aligned lipid bilayer samples. One-dimensional dipolar waves are an extension of two-dimensional PISA (polarity index slant angle) wheels that map protein structures in NMR spectra of both weakly and completely aligned samples. Dipolar waves describe the periodic wave-like variations of the magnitudes of the heteronuclear dipolar couplings as a function of residue number in the absence of chemical shift effects. Since weakly aligned samples of proteins display these same effects, primarily as residual dipolar couplings, in solution NMR spectra, this represents a convergence of solid-state and solution NMR approaches to structure determination.Key words: NMR spectroscopy, protein structure, dipolar couplings, membrane proteins, structure determination.


1972 ◽  
Vol 50 (18) ◽  
pp. 2232-2234 ◽  
Author(s):  
Gerald F. Dionne

The argument that Ti3+ ions produce 12 magnetic complexes when substituted for Al3+ in CsAl (SO4)2∙12H2O (Cs alum) is supported neither by experimental evidence nor a realistic physical model. The uniform intensity of the superhyperfine structure in Rb(TiAl) alum disproves the idea that titanium nuclei are involved because the natural abundance of nuclear magnetic isotopes is only 13%. In addition, the magnitudes of the splittings are too small to represent electron–nuclear spin interactions within the Ti3+ ions.


2014 ◽  
Vol 59 (2) ◽  
pp. 57-73 ◽  
Author(s):  
Christopher L. Suiter ◽  
Sivakumar Paramasivam ◽  
Guangjin Hou ◽  
Shangjin Sun ◽  
David Rice ◽  
...  

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