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揭示溶液中吲哚的激发态动力学。

Unveiling the Excited State Dynamics of Indole in Solution.

机构信息

Department of Chemistry, Sapienza University of Rome, Rome 00185, Italy.

Department of Technological and Chemical Sciences, Tor Vergata University of Rome, Rome 00133, Italy.

出版信息

J Chem Theory Comput. 2023 Jul 11;19(13):4114-4124. doi: 10.1021/acs.jctc.3c00221. Epub 2023 Jun 17.

Abstract

In this paper, we reconstruct in detail the dynamics of the emitting electronic excited state of aqueous indole, investigating its relaxation mechanism and kinetics to be related to the time-dependent fluorescence signal. Taking advantage of the results shown in a very recent paper, we were able to model the relaxation process in solution in terms of the transitions between two gas-phase singlet electronic states (L and L), subsequently irreversibly relaxing to the gas-phase singlet dark state (πσ*). A comparison of the results with the available experimental data shows that the relaxation mechanism we obtain by our theoretical-computational model is reliable, reproducing rather accurately all the experimental observables.

摘要

在本文中,我们详细重建了水合吲哚发射电子激发态的动力学,研究了其弛豫机制和动力学,以与时间相关的荧光信号相关。利用最近一篇论文中的结果,我们能够根据两个气相单重电子态(L 和 L)之间的跃迁来模拟溶液中的弛豫过程,随后不可逆地弛豫到气相单重暗态(πσ*)。将结果与现有实验数据进行比较表明,我们的理论计算模型得到的弛豫机制是可靠的,能够相当准确地再现所有实验可观测结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ebf/10339669/2c8cc863c1f6/ct3c00221_0001.jpg

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