Kim Taiho, Felker Peter M
Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095-1569, USA.
J Phys Chem A. 2007 Dec 13;111(49):12466-70. doi: 10.1021/jp075053i. Epub 2007 Oct 9.
We report stimulated Raman spectra at 0.2 and 0.03 cm(-1) resolution in the CH-stretching region of jet-cooled fluorene. The results were obtained by a version of ionization-gain stimulated Raman spectroscopy in which resonant two-photon ionization probing of the state-population changes arising from stimulated Raman transitions is assisted by the process of intramolecular vibrational redistribution (IVR) in the Raman-excited molecule. The fluorene spectra reveal extensive vibrational coupling interactions involving both the aliphatic and aromatic CH-stretching first excited states with nearby background states. Results pertaining to the symmetric aliphatic CH-stretching fundamental are consistent with a tier model of IVR and point to vibrational energy flow out of the CH stretch on a approximately 1 ps time scale with subsequent redistribution on a approximately 5 ps time scale.
我们报道了在喷射冷却芴的CH拉伸区域中分辨率为0.2和0.03 cm⁻¹的受激拉曼光谱。结果是通过一种电离增益受激拉曼光谱法获得的,其中受激拉曼跃迁引起的态布居变化的共振双光子电离探测借助于拉曼激发分子中的分子内振动再分布(IVR)过程。芴的光谱揭示了广泛的振动耦合相互作用,涉及脂肪族和芳香族CH拉伸的第一激发态与附近的背景态。与对称脂肪族CH拉伸基频相关的结果与IVR的层级模型一致,并表明振动能量在大约1 ps的时间尺度上从CH拉伸流出,随后在大约5 ps的时间尺度上重新分布。