Fushitani Mizuho, Miyamoto Yuki, Hoshina Hiromichi, Momose Takamasa
Department of Chemistry, Graduate School of Science, Kyoto University, Kyoto 606-8502, Japan.
J Phys Chem A. 2007 Dec 13;111(49):12629-34. doi: 10.1021/jp0761113. Epub 2007 Nov 13.
Photochemical reactions of molecules in solid orthodeuterium (o-D2) have been studied by high-resolution infrared spectroscopy and compared with previous results obtained in solid parahydrogen (p-H2). Ultraviolet photolysis of CD3I molecules in solid o-D2 yielded CD3 radicals and iodine atoms efficiently, which indicates a small cage effect in solid o-D2, as in the case of solid p-H2. The Fourier transform infrared spectrum of the nu3 vibrational band of CD3 showed a rotational structure with additional splitting due to crystal field interactions. The magnetic dipole transition (2P1/2<--2P3/2) of the I atom isolated in solid o-D2 was observed together with a strong rotational satellite of deuterium molecules through the electron-roton coupling in solid hydrogen. The tunneling reaction between CD3 and D2 was not observed in a time scale of a few days, which gives the upper limit of the tunneling reaction rate of 10(-8) s(-1) at 4.2 K.
通过高分辨率红外光谱研究了固体正氘(o-D₂)中分子的光化学反应,并与之前在固体仲氢(p-H₂)中获得的结果进行了比较。固体o-D₂中CD₃I分子的紫外光解有效地产生了CD₃自由基和碘原子,这表明固体o-D₂中的笼效应较小,与固体p-H₂的情况相同。CD₃的ν₃振动带的傅里叶变换红外光谱显示出由于晶体场相互作用而产生额外分裂的转动结构。通过固体氢中的电子-罗顿耦合,观察到了固体o-D₂中孤立的I原子的磁偶极跃迁(2P₁/₂←--2P₃/₂)以及氘分子的强转动卫星峰。在几天的时间尺度内未观察到CD₃与D₂之间的隧穿反应,这给出了4.2 K时隧穿反应速率的上限为10⁻⁸ s⁻¹。