A study of 14N relaxation and nitrogen–proton spin coupling in nucleoside, indole, and ε-caprolactam systems through Fourier transform measurements of NH proton spin–lattice relaxation in the rotating frame

1978 ◽  
Vol 56 (9) ◽  
pp. 1302-1305 ◽  
Author(s):  
Michael Eugene Moseley ◽  
Peter Stilbs
Keyword(s):  
Relaxation Times ◽  
Lattice Relaxation ◽  
Proton Spin ◽  
Coupling Constants ◽  
Spin Coupling ◽  
Spin Lattice Relaxation ◽  
Indole Derivatives ◽  
Spin Lattice ◽  
Proton Coupling ◽  
Nuclear Spin Lattice Relaxation

Measurements of nitrogen-14 nuclear spin–lattice relaxation times and direct proton coupling constants are presented for a series of nucleosides and nucleoside bases and indole derivatives in DMSO-d6 and for a series of ε-caprolactam concentrations in CDCl3. The data were obtained through NH proton T1ρ measurements, a potentially useful alternative to direct 14N and 15N nuclear magnetic resonance for the study of e.g. NH hydrogen bonding.

A study of 14N relaxation and nitrogen–proton spin coupling in Watson–Crick base pair models through Fourier transform measurements on NH proton spin–lattice relaxation in the rotating frame

1979 ◽  
Vol 57 (9) ◽  
pp. 1075-1079 ◽  
Author(s):  
Michael E. Moseley ◽  
Peter Stilbs
Keyword(s):  
Relaxation Times ◽  
Lattice Relaxation ◽  
Proton Spin ◽  
Coupling Constants ◽  
Spin Coupling ◽  
Spin Lattice Relaxation ◽  
Indirect Measurements ◽  
Spin Lattice ◽  
Proton Coupling ◽  
Nuclear Spin Lattice Relaxation

Indirect measurements of nitrogen-14 nuclear spin-lattice relaxation times and direct proton coupling constants are presented together with carbon-13 T1 data for a series of alkyl-substituted nucleic acid bases and mixtures thereof in DMSO-d6. With the exception of the guanine NH nitrogen, which possibly experiences a decrease in the electric field gradient upon complexation with cytosine, no indications of significant changes in the electronic environment around the nitrogen nuclei were found for any combination of bases. Forsen–Hoffman spin saturation transfer experiments on the NH and NH2 protons are also presented.

Deuterium Nuclear Spin–Lattice Relaxation Times and Quadrupolar Coupling Constants in Isotopically Labeled Saccharides

2000 ◽  
Vol 144 (2) ◽  
pp. 207-216 ◽  
Author(s):  
Bidisha Bose-Basu ◽  
Jaroslav Zajicek ◽  
Gail Bondo ◽  
Shikai Zhao ◽  
Meredith Kubsch ◽  
...  
Keyword(s):  
Nuclear Spin ◽  
Relaxation Times ◽  
Lattice Relaxation ◽  
Coupling Constants ◽  
Spin Lattice Relaxation ◽  
Spin Lattice ◽  
Quadrupolar Coupling ◽  
Nuclear Spin Lattice Relaxation

Scalar Second-Kind Relaxation of 27Al, 69Ga and 71Ga Nuclei in Aluminium and Gallium Complexes

1983 ◽  
Vol 38 (10) ◽  
pp. 1173-1181 ◽  
Author(s):  
V. P. Tarasov ◽  
V. I. Privalov ◽  
G. A. Kirakosyan ◽  
Yu. A. Buslaev
Keyword(s):  
Relaxation Times ◽  
Lattice Relaxation ◽  
Coupling Constants ◽  
Spin Coupling ◽  
Spin Lattice Relaxation ◽  
Nuclear Spins ◽  
Quadrupole Relaxation ◽  
Spin Lattice ◽  
Exchange Processes ◽  
Scalar Contribution

Abstract Spin-spin and spin-lattice relaxation times of nuclei 69,71Ga, 27Al, 14N in anions [MClnBr4-n]-and the solvate complexes [M(CH3CN)6]3+, produced from dissolution of MCl3 and MBr3 in the mixture CH3CN + CH3NO2 (M = Ga, Al), are measured in the temperature range from -40 up to + 70 °C. It is shown that nuclear spins of 69,71Ga, 27Al relax in the anionic and cationic complexes by means of the second-kind scalar and quadrupole relaxation mechanisms (due to the relaxation of the nuclei 35,37Cl, 79,81Br, 14N). The complexes [MClnBr4-n]-and [M(CH3CN)6]3+ in the investigated solutions are inert and do not undergo exchange processes in the NMR time scale. The scalar spin coupling constants in [M(CH3CN)6]3+ are determined from the scalar contribution to the relaxation rate of 69,71Ga, 27Al, and the measured relaxation time of 14N in the solvate complex; the results are J(69Ga-14N) = 59 ± 5 Hz, J(71Ga-14N) = 74 ± 6Hz, J(27Al-14N) = 22 ± 2Hz.

1H–1H internuclear distance measurements in carbohydrates: proton transient nuclear Overhauser enhancement and spin-lattice relaxation in (13C)- and (2H)-substituted compounds

1990 ◽  
Vol 68 (12) ◽  
pp. 2171-2182 ◽  
Author(s):  
Paul C. Kline ◽  
Anthony S. Serianni ◽  
Shaw-Guang Huang ◽  
Michael Hayes ◽  
Robert Barker
Keyword(s):  
Relaxation Times ◽  
Lattice Relaxation ◽  
Coupling Constants ◽  
Spin Coupling ◽  
Spin Lattice Relaxation ◽  
Substitution Effects ◽  
Distance Measurements ◽  
Spin Lattice ◽  
Nuclear Overhauser Enhancement ◽  
Nuclear Overhauser

Proton transient nuclear Overhauser enhancement (TnOe) and spin-lattice relaxation times (T1) have been used to evaluate the conformations of several monosaccharides and disaccharides containing (13C) and (2H) substitution. Absolute 1H–1H internuclear distances were determined by TnOe and DESERT (deuterium substitution effects on relaxation times) experiments on conformationally rigid methyl β-D-galactopyranoside and α- and β-D-xyloses, respectively. The DESERT method was extended to examine O-glycoside conformation in two blood-group disaccharides that were prepared enzymically with (13C) and (or) (2H) substitution. Preferred disaccharide conformations deduced from these distance measurements are compared to those determined from 13C–13C and 13C–1H spin coupling constants, theoretical calculations, and crystallographic studies. Keywords: TnOe, DESERT, carbohydrate conformation.

PROTON SPIN-LATTICE RELAXATION TIMES OF HUMIC ACIDS AS DETERMINED BY SOLUTION NMR

Soil Science ◽  
2003 ◽  
Vol 168 (2) ◽  
pp. 128-136 ◽  
Author(s):  
Kaijun Wang ◽  
L. Charles Dickinson ◽  
Elham A. Ghabbour ◽  
Geoffrey Davies ◽  
Baoshan Xing
Keyword(s):  
Humic Acids ◽  
Relaxation Times ◽  
Lattice Relaxation ◽  
Proton Spin ◽  
Spin Lattice Relaxation ◽  
Solution Nmr ◽  
Spin Lattice
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