Solid-state NMR of endohedral hydrogen-fullerene complexes

被引:60
|
作者
Carravetta, M.
Danquigny, A.
Mamone, S.
Cuda, F.
Johannessen, O. G.
Heinmaa, I.
Panesar, K.
Stern, R.
Grossel, M. C.
Horsewill, A. J.
Samoson, A.
Murata, M.
Murata, Y.
Komatsu, K.
Levitt, M. H. [1 ]
机构
[1] Univ Southampton, Sch Chem, Southampton SO17 1BJ, Hants, England
[2] NICPB, EE-12618 Tallinn, Estonia
[3] Univ Nottingham, Dept Phys, Nottingham NG7 2RD, England
[4] Kyoto Univ, Kyoto 6110011, Japan
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1039/b707075f
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
We present an overview of solid-state NMR studies of endohedral H-2-fullerene complexes, including H-1 and C-13 NMR spectra, H-1 and C-13 spin relaxation studies, and the results of H-1 dipole-dipole recoupling experiments. The available data involves three different endohedral H-2-fullerene complexes, studied over a wide range of temperatures and applied magnetic fields. The symmetry of the cage influences strongly the motionally-averaged nuclear spin interactions of the endohedral H-2 species, as well as its spin relaxation behaviour. In addition, the non-bonding interactions between fullerene cages are influenced by the presence of endohedral hydrogen molecules. The review also presents several pieces of experimental data which are not yet understood, one example being the structured H-1 NMR lineshapes of enclohedral H-2 molecules trapped in highly symmetric cages at cryogenic temperatures. This review demonstrates the richness of NMR phenomena displayed by H-2-fullerene complexes, especially in the cryogenic regime.
引用
收藏
页码:4879 / 4894
页数:16
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