Observation of 2izsz order in NMR relaxation studies for measuring cross-correlation of chemical shift anisotropy and dipolar interactions

1987 ◽  
Vol 138 (6) ◽  
pp. 601-606 ◽  
Author(s):  
Guy Jaccard ◽  
Stephen Wimperis ◽  
Geoffrey Bodenhausen
Keyword(s):  
Chemical Shift ◽  
Cross Correlation ◽  
Chemical Shift Anisotropy ◽  
Nmr Relaxation ◽  
Dipolar Interactions ◽  
Relaxation Studies

Temperature Dependence of Molecular Conformation, Dynamics, and Chemical Shift Anisotropy of α,α-Trehalose in D2O by NMR Relaxation

1997 ◽  
Vol 119 (6) ◽  
pp. 1336-1345 ◽  
Author(s):  
Gyula Batta ◽  
Katalin E. Kövér ◽  
Jacquelyn Gervay ◽  
Miklós Hornyák ◽  
Gareth M. Roberts
Keyword(s):  
Chemical Shift ◽  
Temperature Dependence ◽  
Molecular Conformation ◽  
Chemical Shift Anisotropy ◽  
Nmr Relaxation

Selenium-77 and phosphorus-31 nuclear spin relaxation in tri-(tert-butyl) phosphine selenide

1991 ◽  
Vol 69 (7) ◽  
pp. 1054-1056 ◽  
Author(s):  
Glenn H. Penner
Keyword(s):  
Chemical Shift ◽  
Nuclear Spin ◽  
Chemical Shift Anisotropy ◽  
Relaxation Times ◽  
Nmr Relaxation ◽  
Lattice Relaxation ◽  
Spin Rotation ◽  
Spin Lattice Relaxation ◽  
Phosphine Selenide ◽  
High Fields

Selenium-77 and phosphorus-31 spin-lattice relaxation times are reported for tri-tert-butylphosphine selenide in chloroform-d, at 303 K and at several different magnetic field strengths. At moderate fields the 31P–1H dipole–dipole, spin-rotation, and chemical shift anisotropy mechanisms contribute significantly towards the 31P T1. At high fields chemical shift anisotropy dominates. The selenium-77 nuclear spin relaxes almost exclusively by spin rotation at low to moderate fields and the chemical shift anisotropy contribution only becomes significant at very high fields. This is due to an unusually small 77Se CSA. The contribution due to 31P–77Se dipole–dipole interactions is small but significant. Key words: 77Se NMR, NMR relaxation, phosphine selenide.

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