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Anisotropic chemical shifts and spin rotation constants of 15N from liquid and solid state NMR: Nitrobenzene

MPG-Autoren
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Schweitzer,  Dieter
Department of Molecular Physics, Max Planck Institute for Medical Research, Max Planck Society;

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Spiess,  Hans W.
MPI for Polymer Research, Max Planck Society;

Externe Ressourcen

http://www.sciencedirect.com/science/article/pii/0022236474900481/pdf?md5=c0b5635283f77acf6f7a8485c495149c&pid=1-s2.0-0022236474900481-main.pdf
(beliebiger Volltext)

https://doi.org/10.1016/0022-2364(74)90048-1
(beliebiger Volltext)

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Zitation

Schweitzer, D., & Spiess, H. W. (1974). Anisotropic chemical shifts and spin rotation constants of 15N from liquid and solid state NMR: Nitrobenzene. Journal of Magnetic Resonance, 16(2), 243-251. doi:10.1016/0022-2364(74)90048-1.


Zitierlink: https://hdl.handle.net/11858/00-001M-0000-002D-E602-6
Zusammenfassung
The study of the 15N spin-lattice relaxation time T1 in nitrobenzene at 14 and 32 MHz from −10 to 60°C showed that at 32 MHz relaxation due to anisotropic chemical shift is predominant. At low frequencies, the relaxation is caused mainly by spin rotation and at low temperature also by intermolecular dipole-dipole interaction. From the powder spectrum in solid nitrobenzene, the principal elements of the shielding tensor σ̂ were obtained: σxx = −273 ± 10 ppm, σyy = +94 ± 10 ppm, and σzz = +156 ± 10 ppm relative to liquid nitrobenzene, . From the almost axially symmetric σ̂-tensor, the spin rotation constants were calculated: C‖ = 11.4 ± 1.5 kHz and C⊥ = 1.35 ± 0.5 kHz, where C‖ is the component parallel to the twofold axis of the molecule. These values for Δσ and the spin rotation constants are in excellent agreement with those obtained by analysis of the relaxation data. A comparison of anisotropic chemical shifts and spin rotation constants for 15N and 13C in isoelectronic compounds is given.