Structure and dynamic role of conical intersections in the πσ*-mediated photodissociation reactions

IF 2.5 2区 化学 Q3 CHEMISTRY, PHYSICAL
Hyun Sik You, Songhee Han, Jungki Yoon, Jeong Sik Lim, Jeongmook Lee, Soyeun Kim, Doo-Sik Ahn, J. Lim, Sang Kyu Kim
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引用次数: 17

Abstract

Conical intersection as a dynamic funnel in nonadiabatic transition dictates many important chemical reaction outputs such as reaction rates, yields, and energy disposals especially for chemical reactions taking place on electronically excited states. Therefore, the energetics and topology of conical intersections have been subjected to intensive theoretical and experimental studies for decades as these things are the keys to understanding and controlling nonadiabatic transitions which are ubiquitous in nature. In this article, we focus on πσ*-mediated photodissociation reactions of thiophenols and thioanisoles. Interestingly, for these chemical systems, the nonadiabatic transition probability can be precisely measured as a function of the excitation energy, giving a great opportunity for spectroscopic characterization of the multi-dimensional conical intersection seam that governs the nonadiabatic transition dynamics of polyatomic molecules. The passage of the reactive flux in the proximity of the conical intersection gives rise to dynamic resonances corresponding to dramatic state-specific increases of the nonadiabatic transition probability. Accordingly, it is found that the electronic and nuclear configurations of the reactive flux and their evolution, coupled to the conical intersection seam, are critical in nonadiabatic transition dynamics. Nonadiabaticity is found to be extremely sensitive to the conformational molecular structure, and this has been demonstrated in the photodissociation dynamics of the chemical derivatives of thiophenol. Intramolecular vibrational redistribution, which is nontrivial in surmounting the reaction barrier, is found to wash out state-specific dynamic resonances, implying the importance of the dynamic interplay between vibrational energy flow and nonadiabatic transition. The experimental results on conical intersection dynamics presented in this review provide many interesting and important issues to be pursued in the near future by both theoreticians and experimentalists.
πσ*介导的光解反应中锥形交点的结构和动力学作用
锥形交点作为非绝热过渡的动态漏斗,决定了许多重要的化学反应输出,如反应速率、产率和能量消耗,特别是发生在电子激发态的化学反应。因此,锥形交点的能量学和拓扑结构几十年来一直受到广泛的理论和实验研究,因为它们是理解和控制自然界中普遍存在的非绝热过渡的关键。本文主要研究了πσ*介导的硫代苯酚和硫代苯甲醚的光解反应。有趣的是,对于这些化学体系,非绝热跃迁概率可以被精确地测量为激发能的函数,为控制多原子分子非绝热跃迁动力学的多维锥形交叉缝的光谱表征提供了很大的机会。在锥形交点附近,反应通量的通过产生了动态共振,对应于非绝热跃迁概率的急剧增加。因此,发现在非绝热跃迁动力学中,与锥形相交缝耦合的反应通量的电子和核构型及其演化是至关重要的。发现非绝热性对构象分子结构极为敏感,这已在噻吩化学衍生物的光解动力学中得到证明。分子内的振动重分布,在克服反应势垒的过程中是非常重要的,它可以冲掉特定态的动态共振,这意味着振动能量流和非绝热跃迁之间的动态相互作用的重要性。本文所介绍的圆锥交动力学的实验结果为今后理论和实验工作者提供了许多有趣和重要的研究方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
14.20
自引率
1.60%
发文量
5
审稿时长
1 months
期刊介绍: International Reviews in Physical Chemistry publishes review articles describing frontier research areas in physical chemistry. Internationally renowned scientists describe their own research in the wider context of the field. The articles are of interest not only to specialists but also to those wishing to read general and authoritative accounts of recent developments in physical chemistry, chemical physics and theoretical chemistry. The journal appeals to research workers, lecturers and research students alike.
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