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Excited State Structural Dynamics of the Charge Transfer State of Peridinin

机译:Peridinin电荷转移态的激发态结构动力学

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摘要

We present infrared and visible transient absorption measurements of the first excited singlet state(S1 and S_(1/ICT))of peridinin in methanol,isopropanol,and chloroform solution following one-photon excitation,using 490 nm light,to excite the S2 state that populates S1 via rapid(~50 fs in methanol)internal conversion.This technique enables the study of subsequent structural dynamics in S1 involved in the formation of the charge transfer state.The S1 lifetime of peridinin in methanol,isopropanol,and chloroform is found to be 12,54,and 65 ps,respectively,as determined by infrared transient absorption.We observe two formation timescales in the S1 state.We attribute the shortest timescale to relaxation following internal conversion and the longer timescale to formation of the S_(1/ICT)state.
机译:我们介绍了在单光子激发后,使用490 nm光激发,在甲醇,异丙醇和氯仿溶液中,peridinin的第一激发单重态(S1和S_(1 / ICT))的红外和可见光瞬态吸收测量通过快速的内部转化(在甲醇中约50 fs)填充S1。这项技术使得能够研究S1中后续的结构动力学,参与电荷转移状态的形成。发现了苦瓜素在甲醇,异丙醇和氯仿中的S1寿命。分别由红外瞬态吸收确定为12,54和65 ps。我们在S1状态观察到两个形成时标。我们将最短的时标归因于内部转换后的弛豫,将更长的时标归因于S_(1 / ICT)状态。

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