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Symmetry-breaking in the endofullerene H2O@C60 revealed in the quantum dynamics of ortho and para-water: a neutron scattering investigation

机译:邻水和对水的量子动力学揭示了富勒烯H2O @ C60中对称性的破坏:中子散射研究

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摘要

Inelastic neutron scattering (INS) has been employed to investigate the quantum dynamics of water molecules permanently entrapped inside the cages of C60 fullerene molecules. This study of the supramolecular complex, H2O@C60, provides the unique opportunity to study isolated water molecules in a highly symmetric environment. Free from strong interactions, the water molecule has a high degree of rotational freedom enabling its nuclear spin isomers, ortho-H2O and para-H2O to be separately identified and studied. The INS technique mediates transitions between the ortho and para spin isomers and using three INS spectrometers, the rotational levels of H2O have been investigated, correlating well with the known levels in gaseous water. The slow process of nuclear spin conversion between ortho-H2O and para-H2O is revealed in the time dependence of the INS peak intensities over periods of many hours. Of particular interest to this study is the observed splitting of the ground state of ortho-H2O, raising the three-fold degeneracy into two states with degeneracy 2 and 1 respectively. This is attributed to a symmetry-breaking interaction of the water environment.
机译:非弹性中子散射(INS)已用于研究永久滞留在C60富勒烯分子笼中的水分子的量子动力学。这项对超分子复合物H2O @ C60的研究为在高度对称的环境中研究孤立的水分子提供了独特的机会。由于没有强烈的相互作用,水分子具有高度的旋转自由度,从而可以分别鉴定和研究其核自旋异构体,邻-H2O和对-H2O。 INS技术介导了正旋异构体和对旋自旋异构体之间的跃迁,并使用三个INS光谱仪对H2O的旋转水平进行了研究,与气态水中的已知水平高度相关。邻水和对水之间核自旋转化的缓慢过程体现在INS峰强度在许多小时内的时间依赖性。这项研究特别有趣的是观察到的邻位H2O基态分裂,将三重简并性提升为简并性分别为2和1的两个状态。这归因于水环境破坏对称性的相互作用。

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