一维贝取代手性 PDI 的电子吸收光谱和圆二色光谱:分子间相互作用、振动耦合和聚合体大小的影响

IF 3.3 3区 化学 Q2 CHEMISTRY, PHYSICAL
Yuchuan Xu, Yi Zhao, WanZhen Liang
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引用次数: 0

摘要

电子圆二色性(ECD)光谱是研究有机手性超分子的首选工具。然而,如何在实验中阐明分子振动运动和分子间相互作用对 ECD 光谱的贡献是一个巨大的挑战,而分子振动运动和分子间相互作用是化学传感器、催化剂或光电子学高效系统结构设计的关键因素。针对这一问题,我们在本文中采用非马尔可夫随机薛定谔方程(NMSSE),针对二重态表示的模型哈密顿,包括分子内局部激发态(LEs)、分子间变化传递激发态(CTEs)和振动耦合(VC),对两种一维畦取代手性过二亚胺(PDIs)的振动分辨吸收和 ECD 光谱进行了理论研究。我们的计算结果表明,加入 VC 效应的理论光谱与实验光谱的吻合程度要好于未加入 VC 效应的光谱,而且两种贝叶取代 PDI 的传统吸收光谱之间的差异远不如它们的 ECD 光谱那么明显,这验证了 ECD 光谱对手性超分子的绝对构型和构象非常敏感。我们进一步比较了用时变密度泛函理论和混合激子模型计算出的不同聚合体尺寸的纯电子能谱,并对 LE 和 CTE 状态进行了解耦。结果表明,LE 和 CTE 状态之间的杂化会导致高能带出现新的峰值或谷值,并且计算出的 ECD 光谱与激子手性规则预测的光谱之间存在显著偏差。研究进一步表明,低聚物的 ECD 光谱会随着聚合体大小的变化而呈现奇偶交替模式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Electronic Absorption and Circular Dichroism Spectra of One-Dimensional Bay-Substituted Chiral PDIs: Effects of Intermolecular Interactions, Vibronic Coupling, and Aggregate Size

Electronic Absorption and Circular Dichroism Spectra of One-Dimensional Bay-Substituted Chiral PDIs: Effects of Intermolecular Interactions, Vibronic Coupling, and Aggregate Size
Electronic circular dichroism (ECD) spectroscopy is the preferred tool for studying organic chiral supramolecules. However, it is a great challenge to experimentally clarify the contributions to ECD spectra from molecular vibrational motions and the intermolecular interactions, key factors for an efficient system architecture design of chemical sensors, catalysts, or optoelectronics. Focusing on this issue, here, we perform theoretical studies on the vibrationally resolved absorption and ECD spectra of two one-dimensional bay-substituted chiral perylene diimides (PDIs) by employing the non-Markovian stochastic Schrödinger equation (NMSSE) with respect to the model Hamiltonian in the diabatic representation, which includes the intramolecular localized excited states (LEs), intermolecular change-transfer excited states (CTEs), and the vibronic couplings (VC) as well. Our calculated results exhibit that the theoretical spectra, with the inclusion of the VC effect, agree better with the experimental ones than those without this effect and that the difference between the traditional absorption spectra of the two bay-substituted PDIs is much less obvious than that in their ECD spectra, verifying that ECD spectroscopy is sensitive to the absolute configuration and conformation of chiral supramolecules. We further make a comparison among the pure electronic spectra of aggregates with different aggregate sizes calculated by the time-dependent density functional theory and the mixed exciton model with and without decoupling the LE and CTE states. It is shown that the hybridization between LE and CTE states results in the emergence of new peaks or troughs in the high-energy band and a significant deviation between the calculated ECD spectrum and that predicted by the exciton chirality rule. It is further shown that the ECD spectra of oligomers exhibit an odd–even alternation pattern with changes in aggregate size.
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来源期刊
The Journal of Physical Chemistry C
The Journal of Physical Chemistry C 化学-材料科学:综合
CiteScore
6.50
自引率
8.10%
发文量
2047
审稿时长
1.8 months
期刊介绍: The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.
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