Anisotropic nuclear spin interactions in H2O@C60 determined by solid-state NMR

被引:10
|
作者
Concistre, M. [1 ]
Mamone, S. [1 ]
Denning, M. [1 ]
Pileio, G. [1 ]
Lei, X. [2 ]
Li, Y. [2 ]
Carravetta, M. [1 ]
Turro, N. J. [2 ]
Levitt, M. H. [1 ]
机构
[1] Univ Southampton, Sch Chem, Southampton SO17 1BJ, Hants, England
[2] Columbia Univ, Dept Chem, New York, NY 10027 USA
基金
英国工程与自然科学研究理事会; 美国国家科学基金会;
关键词
solid-state NMR; endohedral water fullerene; spin interaction; MAGNETIC-RESONANCE; FULLERENE; HYDROGEN;
D O I
10.1098/rsta.2012.0102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We report a solid-state NMR study of the anisotropic nuclear spin interactions in H2O@C-60 at room temperature. We find evidence of significant dipole-dipole interactions between the water protons, and also a proton chemical shift anisotropy (CSA) interaction. The principal axes of these interaction tensors are found to be perpendicular. The magnitude of the CSA is too large to be explained by a model in which the water molecules are partially aligned with respect to an external axis. The evidence indicates that the observed CSA is caused by a distortion of the geometry or electronic structure of the fullerene cages, in response to the presence of the endohedral water.
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页数:11
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