The spin-lattice relaxation of ten polychloroalkanes (ethanes to pentanes) have been studied both neat and in a 50% solution in CDC13. The Tl values for the CH,, CH,Cl and CHCl, carbons decrease with increasing molecular weight in accordance with a dipolar-dominated mechanism, whereas those of the C
13C Spin—lattice relaxation behaviour of pyridine and tetrahydrofurane
✍ Scribed by E. von Goldammer; H.-D. Lüdemann; O. Röder
- Publisher
- Elsevier Science
- Year
- 1974
- Tongue
- English
- Weight
- 491 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
Spin-lattice relaxation times of 13C nuclei in pyridine and tetrahydrofurane
have been measured at various temperatures. Mainly dipole-dipole interaction was found to influence the relaxation behaviour below 273°K. Spinrotation, which predominates at higher temperatures, was found to contribute about 25% to the measured relaxation rates at room temperature. The components of the spin-rotation coupling constant, ~11 and cl have been determined for pure pyridine, using :esults from 'H and 14N relaxation. Anisotropic rotational diffusion was found for both organic molecules in their mixtures with water.
📜 SIMILAR VOLUMES
## Spin-lattice relaxation times of t3C nuclei in organic compounds have been measured in a wide temperature range. The dipole-dipole interaction with protons is predominant at lower temperatures and the spin-rotation interaction at higher temperatures. Both the measured relaxation times and r3C c
The paper is devoted to investigations of spin-lattice relaxation ation determined by nuclear dipole-dipole interactions for processes in 99% 13 C-enriched diamonds. Relaxation time measpin-1 2 nuclei and T imp 1 is the impurity component of the spinsurements were performed as a function of orientat