Physical and Theoretical Chemistry Laboratory, Oxford University , South Parks Road, Oxford OX1 3QZ, U.K.
J Am Chem Soc. 2015 Mar 4;137(8):2886-91. doi: 10.1021/ja508941k. Epub 2015 Feb 20.
Conical intersections play a crucial role in photochemical processes, but limited experimental information exists on the structural distortions that couple electronic with reactive nuclear motion. Using ultra-broadband and highly time-resolved optical spectroscopy, we follow the evolution of vibrational wavepackets after passage through a conical intersection during the primary visual event, the 11-cis to all-trans photoisomerization of the retinal chromophore in rhodopsin. Comparison of nuclear coherences generated under resonant and off-resonant impulsive excitation conclusively reveals coherent wavepacket motion in the bathorhodopsin photoproduct over the full vibrational manifold. We observe strongly enhanced coherences in low-frequency torsional degrees of freedom over the fingerprint region and almost complete suppression of some hydrogen wagging motion. Our ability to monitor the multidimensional evolution of nuclear wavepackets across multiple electronic states is a general means for studying the structural and dynamic origins of efficient photochemistry and provides critical experimental information for theoretical studies.
圆锥交叉在光化学反应过程中起着至关重要的作用,但关于电子与反应核运动耦合的结构变形的实验信息有限。使用超宽带和高度时间分辨的光学光谱,我们在视紫红质中视黄醛的 11-顺式到全反式光异构化的主要视觉事件期间,通过圆锥交叉后,跟踪振动波包的演化。在共振和非共振脉冲激发下产生的核相干的比较,明确揭示了在完整的振动简并中,bathorhodopsin 光产物中相干波包的运动。我们观察到指纹区域中低频扭转自由度的相干性大大增强,并且一些氢摇摆运动几乎完全被抑制。我们能够监测跨越多个电子态的核波包的多维演化,这是研究高效光化学的结构和动力学起源的一般手段,并为理论研究提供了关键的实验信息。