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利用时间分辨脉冲受激拉曼光谱追踪四极苝二酰亚胺对称破缺电荷分离过程中的结构演化

Tracking Structural Evolution during Symmetry-Breaking Charge Separation in Quadrupolar Perylene Bisimide with Time-Resolved Impulsive Stimulated Raman Spectroscopy.

作者信息

Kim Woojae, Kim Taeyeon, Kang Seongsoo, Hong Yongseok, Würthner Frank, Kim Dongho

机构信息

Department of Chemistry, Spectroscopy Laboratory for Functional π-Electronic Systems, Yonsei University, 03722, Seoul, Korea.

Institut für Organische Chemie & Center for, Nanosystems Chemistry, Universität Würzburg, Am Hubland, 97074, Würzburg, Germany.

出版信息

Angew Chem Int Ed Engl. 2020 May 25;59(22):8571-8578. doi: 10.1002/anie.202002733. Epub 2020 Apr 28.

Abstract

Elucidating structural roles in photoinduced charge transfer is indispensable, as nuclear rearrangements are simultaneously usually involved in the dynamics. However, it is hard to evaluate whether the structural changes occur or not by using conventional time-resolved electronic spectroscopy. Here, time-resolved impulsive stimulated Raman spectroscopy is applied to record the evolution of vibrational snapshots during charge-separation dynamics of donor-acceptor-donor-type quadrupolar perylene bisimide in real time. Drastic frequency shifts were observed for several Raman bands with their population kinetics, thus symmetry-breaking charge separation accompanies significant structural changes, as supported by (TD)-DFT calculations. A comparison between time-resolved Raman spectra of the neutral S state and the radical anion species shows that the spectral signatures, especially in high-frequency regions, provide important clues to bond length alternation patterns in the PBI core.

摘要

阐明光诱导电荷转移中的结构作用是必不可少的,因为核重排通常同时参与动力学过程。然而,使用传统的时间分辨电子光谱很难评估结构变化是否发生。在此,应用时间分辨脉冲受激拉曼光谱实时记录供体-受体-供体型四极苝二酰亚胺电荷分离动力学过程中振动快照的演变。观察到几个拉曼带及其布居动力学有剧烈的频率变化,因此,如(TD)-DFT计算所支持的那样,对称性破缺的电荷分离伴随着显著的结构变化。中性S态和自由基阴离子物种的时间分辨拉曼光谱之间的比较表明,光谱特征,特别是在高频区域,为PBI核中的键长交替模式提供了重要线索。

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