Stallhofer Klara, Nuber Matthias, Schüppel Franziska, Thumser Stefan, Iglev Hristo, de Vivie-Riedle Regina, Zinth Wolfgang, Dube Henry
Physik-Department, Lehrstuhl für Laser- und Röntgenphysik, Technische Universität München, James-Franck-Str. 1, 85748 Garching, Germany.
Department für Chemie, Ludwig-Maximilians-Universität München, Butenandtstr. 5-13, 81377 Munich, Germany.
J Phys Chem A. 2021 May 27;125(20):4390-4400. doi: 10.1021/acs.jpca.1c02646. Epub 2021 May 14.
Deciphering the exact electronic and geometric changes of photoexcited molecules is an important task not only to understand the fundamental atomistic mechanisms but also to rationally design molecular properties and functions. Here, we present a combined experimental and theoretical study of the twisted intramolecular charge transfer (TICT) process in hemithioindigo photoswitches. Using ultrafast transient IR spectroscopy as the main analytical method, a detailed understanding of the extent and direction of charge transfer within the excited molecule is obtained. At the same time, the geometrical distortion is monitored directly via changes of indicative vibrational modes over the time course of the photoreaction. These high-resolution data deliver a detailed molecular movie of the TICT process in this important class of chromophores with picosecond time resolution.
解析光激发分子的确切电子和几何变化不仅是理解基本原子机制的重要任务,也是合理设计分子性质和功能的重要任务。在此,我们展示了对半硫靛光开关中扭曲分子内电荷转移(TICT)过程的实验与理论相结合的研究。使用超快瞬态红外光谱作为主要分析方法,我们详细了解了激发分子内电荷转移的程度和方向。同时,通过光反应过程中指示性振动模式的变化直接监测几何畸变。这些高分辨率数据以皮秒时间分辨率提供了这一重要发色团类中TICT过程的详细分子动态。