Department of Chemistry, Technische Universität München, D-85747 Garching, Germany.
J Chem Phys. 2017 Feb 28;146(8):084105. doi: 10.1063/1.4976317.
We theoretically investigate the feasibility of characterizing conical intersections with time-resolved resonant femtosecond stimulated Raman spectroscopy (FSRS) using an intense actinic pump pulse. We perform nonperturbative numerical simulations of FSRS signals for a three-electronic-state two-vibrational-mode model, which is inspired by the S(ππ)-S(nπ) conical intersection in pyrazine. Our results show that moderately strong actinic pulses increase the intensity of vibrational fingerprint lines in FSRS transients. They facilitate the extraction of useful spectroscopic information by enhancing peaks revealing the coupling and tuning modes of the conical intersection.
我们从理论上研究了使用强激发脉冲的时间分辨共振飞秒受激拉曼光谱(FSRS)来描述圆锥交叉的可行性。我们对受激拉曼光谱信号进行了非微扰数值模拟,该模型基于吡嗪中的 S(ππ)-S(nπ)圆锥交叉,采用了三电子态两振动模式模型。我们的结果表明,中等强度的激发脉冲会增加 FSRS 瞬态中振动指纹线的强度。它们通过增强揭示圆锥交叉耦合和调谐模式的峰,促进了有用光谱信息的提取。