A deuteron NMR study of the tetrahydrofuran clathrate hydrate - Part I: Relaxation pathways

被引:26
作者
Kirschgen, TM
Zeidler, MD
Geil, B
Fujara, F
机构
[1] Rhein Westfal TH Aachen, Inst Phys Chem, D-52056 Aachen, Germany
[2] Tech Univ Darmstadt, Inst Festkorperphys, D-64289 Darmstadt, Germany
关键词
D O I
10.1039/b212471h
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Longitudinal H-2-relaxation rates 1/T-1 of the polycrystalline clathrate hydrates THF-h(8).17D(2)O and THF-d(8).17H(2)O have been recorded at 55.3 MHz over the temperature range 20 K to 250 K. In spite of the generally dominating intramolecular quadrupolar relaxation mechanism of the deuteron, intermolecular dipolar contributions to relaxation have been observed. The effect is most obvious for the lattice-forming D2O molecules which become immobile at lower temperatures while the guest molecules still perform fast reorientations.
引用
收藏
页码:5243 / 5246
页数:4
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