日本語
 
Help Privacy Policy ポリシー/免責事項
  詳細検索ブラウズ

アイテム詳細


公開

学術論文

Initial conditions for carbon-13 MAS NMR 1D exchange involving chemically equivalent and inequivalent nuclei.

MPS-Authors
/persons/resource/persons128263

Zimmermann,  Herbert
Emeritus Group Biophysics, Max Planck Institute for Medical Research, Max Planck Society;

Fulltext (restricted access)
There are currently no full texts shared for your IP range.
フルテキスト (公開)
公開されているフルテキストはありません
付随資料 (公開)
There is no public supplementary material available
引用

Tekely, P., Reichert, D., Zimmermann, H., & Luz, Z. (2000). Initial conditions for carbon-13 MAS NMR 1D exchange involving chemically equivalent and inequivalent nuclei. Journal of Magnetic Resonance, 145(2), 173-183. doi:10.1006/jmre.2000.2092.


引用: https://hdl.handle.net/11858/00-001M-0000-0028-2AB1-0
要旨
A major problem in dynamic 1D (13)C MAS NMR concerns the exchange between magnetically inequivalent, but chemically equivalent sites, whose signals are not resolved in the regular 1D spectrum. This difficulty may be overcome by properly preparing the initial nonequilibrium state of the spin system in the exchange experiments. In the present paper we discuss the advantages and limitations of several such experiments already in use and propose a new sequence, which we term SELDOM−ODESSA. Unlike the other 1D−exchange methods, this experiment yields pure absorption spectra that can more readily be analyzed quantitatively. The experiment is a hybrid comprising a SELDOM sequence, for selective excitation of one of the spinning sideband manifolds in the spectrum, followed by the ODESSA sequence, which induces alternate polarization in the excited sideband manifold. The evolution of the spectrum following this sequence provides information on both the exchange between congruent sites belonging to the same group of equivalent nuclei, and the exchange between inequivalent sites. Results are presented for a tropolone sample specifically enriched in carbon−13 at the carbonyl and hydroxyl sites. The dominant exchange mechanism in this sample involves spin diffusion. The various spin exchange processes in this sample, in the presence and absence of proton decoupling during the mixing time, are measured and discussed