Chemical Resources Laboratory, Tokyo Institute of Technology, Yokohama 226-8503, Japan.
Phys Chem Chem Phys. 2011 Feb 21;13(7):2744-7. doi: 10.1039/c0cp01961e. Epub 2010 Dec 10.
The dynamics of the intermolecular motion of the phenol(+)-Kr cation generated by photoionization of the neutral π-structure is probed by picosecond time-resolved infrared spectroscopy. The spectrum at zero delay displays only the free OH stretch band of the π-structure. The appearance of the hydrogen-bonded OH stretch band of the H-structure after a few ps is due to ionization-induced π → H site switching. Spectra at long delay (>20 ns) show that the Kr atom delocalizes from one π-site of the aromatic ring to the opposite π-site via the OH-site, like a pendular motion in the classical picture.
通过光解中性π结构生成的苯酚 (+)-Kr 阳离子的分子间运动动力学,采用皮秒时间分辨红外光谱进行了探测。零延迟时的光谱仅显示了 π 结构的游离 OH 伸缩带。几皮秒后,H 结构的氢键 OH 伸缩带的出现是由于电离诱导的 π → H 位切换。长延迟(>20 ns)的光谱表明,Kr 原子通过 OH 位从芳环的一个 π 位离域到相反的 π 位,就像经典图像中的钟摆运动一样。