Additional insights from very-high-resolution 13C NMR spectra of long-chain n-alkanes
Article first published online: 25 JUL 2013
Copyright © 2013 John Wiley & Sons, Ltd.
Magnetic Resonance in Chemistry
Volume 51, Issue 10, pages 605–613, October 2013
How to Cite
Alemany, L. B. (2013), Additional insights from very-high-resolution 13C NMR spectra of long-chain n-alkanes. Magn. Reson. Chem., 51: 605–613. doi: 10.1002/mrc.3988
- Issue published online: 10 SEP 2013
- Article first published online: 25 JUL 2013
- Manuscript Accepted: 24 JUN 2013
- Manuscript Revised: 20 JUN 2013
- Manuscript Received: 27 MAR 2013
- long-chain alkanes;
- very high resolution
New information has been obtained from very-high-resolution 13C NMR studies of a series of long-chain n-alkanes. These compounds are fundamentally important in the petroleum industry and are essential to the life of some plants, flowers, and insects. At least partial resolution of the ten different 13C NMR signals of n-C20H42 is observed at 11.7 T for solutions in C6D6 or C6D5CD3. A 13C T1 inversion-recovery experiment provides much more detailed information than in previous studies of long-chain n-alkanes, demonstrates a steady increase in the relaxation times of the ten different carbons proceeding from the middle to the end of the chain because of segmental motion, and thus confirms the assignments for the interior carbons. In contrast, there is significant overlap for the signals for C-7 and the more interior carbons in a solution of n-C16 or longer chain alkanes in CDCl3. Not only are the chemical shifts sensitive to the solvent used, but also the relative chemical shifts change. Signals for the interior carbons of the odd-number alkanes in CDCl3 are better resolved than in the spectra of their even-number counterparts. Some mixed aromatic solvent systems give increased dispersion of the cluster of C-6 through C-10 signals of n-C20H42, n-C21H44, and n-C22H46. However, none of the solvents used could even partially resolve the C-10 and C-11 signals of n-C21H44 or n-C22H46 at 11.7 T, which may result from a different distribution of conformers for n-C21H44 or n-C22H46 than for n-C20H42 and shorter n-alkanes. Copyright © 2013 John Wiley & Sons, Ltd.