Department of Chemistry, University of Michigan, 930 North University Avenue, Ann Arbor, Michigan 40109, USA.
J Am Chem Soc. 2010 Sep 22;132(37):12784-5. doi: 10.1021/ja1043853.
We present the first implementation of transient vibrational Stark-effect spectroscopy as an ultrafast probe of solvation dynamics. The method is applied to the phototriggered intramolecular charge-transfer reaction of Betaine-30, where the vibrational Stark shifts of the nearby solvent molecules--arising from the change in the electrostatic environment--are measured using a three-pulse photon echo probe. This new experiment provides a direct subpicosecond measure of the chromophore's excited-state dynamics and back electron transfer as viewed from the solvent's perspective. We develop a simple ab initio model that offers semiquantitative prediction of the experimental Stark shifts.
我们首次实现了瞬态振动斯塔克效应光谱学,将其作为超快溶剂动力学探针。该方法应用于甜菜碱-30 的光触发分子内电荷转移反应中,通过三脉冲光子回波探针测量附近溶剂分子的振动斯塔克位移,这是由于静电环境的变化而产生的。这种新实验提供了一种直接的亚皮秒测量方法,用于观察发色团的激发态动力学和从溶剂角度来看的反向电子转移。我们开发了一个简单的从头算模型,该模型可以对半定量地预测实验中的斯塔克位移。