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通过增强电子跃迁偶极矩提高圆二色响应

Boost of Chiroptical Responses Through the Enhancement of Electron Transition Dipole Moment.

作者信息

Gómez-Oya Iván, Portela-Pino Julia, Salonen Laura M, Peña-Gallego Ángeles, Alonso-Gómez José Lorenzo

机构信息

Departamento de Química Orgánica, Universidade de Vigo, Vigo, 36310, Spain.

Departamento de Química Física, Universidade de Vigo, Vigo, 36310, Spain.

出版信息

Chemistry. 2025 Jul 2;31(37):e202501266. doi: 10.1002/chem.202501266. Epub 2025 May 24.

Abstract

The development of robust chiroptical systems is crucial for advancing optoelectronic technologies. Spirobifluorenes (SBFs) have proven to be versatile scaffolds for the construction of a wide variety of robust axially chiral compounds presenting strong chiroptical responses. Herein, we present a strategy for boosting the chiroptical responses via enhancing electric transition dipole moment (ETDM) of interacting chromophores in C-symmetric SBFs presenting exciton coupling. To experimentally validate this approach, we peripherally extended the SBF scaffold through Knoevenagel condensation with the aim of increasing the ETDM of the featured chromophores. The influence of the functionalization on the ETDM was investigated using a combination of computational modeling and experimental techniques, enabling a detailed examination of the relationship between molecular structure and chiroptical properties. Our results demonstrate that peripheral functionalization of SBFs significantly enhances the electric transition dipole moment (ETDM) of the constituent chromophores, with each incremental increase in ETDM resulting in a five-fold enhancement of the g-factor, thereby substantially amplifying the overall chiroptical activity. This straightforward strategy underscores the importance of the ETDM of interacting chromophores in fine-tuning the optoelectronic properties and provides a promising avenue for the rational design of high-performance chiroptical materials.

摘要

强大的手性光学系统的发展对于推进光电子技术至关重要。螺二芴(SBFs)已被证明是构建各种具有强手性光学响应的稳健轴向手性化合物的通用支架。在此,我们提出了一种策略,通过增强具有激子耦合的C对称SBFs中相互作用发色团的电跃迁偶极矩(ETDM)来增强手性光学响应。为了通过实验验证这种方法,我们通过克诺文纳格尔缩合反应对外围扩展SBF支架,目的是增加特色发色团的ETDM。使用计算建模和实验技术相结合的方法研究了功能化对ETDM的影响,从而能够详细考察分子结构与手性光学性质之间的关系。我们的结果表明,SBFs的外围功能化显著增强了组成发色团的电跃迁偶极矩(ETDM),ETDM的每一次增量增加都会导致g因子提高五倍,从而大幅放大整体手性光学活性。这种直接的策略强调了相互作用发色团的ETDM在微调光电子性质方面的重要性,并为高性能手性光学材料的合理设计提供了一条有前景的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/877d/12223341/a3245fe42655/CHEM-31-e202501266-g004.jpg

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