共轭聚合物的手性表达与其聚集类型的联系

IF 5.2 1区 化学 Q1 POLYMER SCIENCE
Annelien van Oosten, Karen Aerts, Yovan de Coene, Thierry Verbiest and Guy Koeckelberghs*, 
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引用次数: 0

摘要

由于其对可见光的强吸收,手性共轭聚合物(CPs)的手性通常用电子圆二色性(ECD)来表达。不幸的是,虽然许多手性CPs在叠加时会产生很强的ECD,但预测和再现最终的行为已被证明是极其困难的。在这里,我们表明CPs的ECD与已知的I型和II型聚集相关。结果表明,I型聚集导致ECD信号具有额外的单信号棉花效应,因此产生不对称频谱。相反,在II型聚合中,产生的ECD信号是对称的。这是确定模型手性CP,聚(3-(3,7-(S)-二甲基辛基)噻吩)的两种方法。此外,两种聚集类型的实际过程是由线性和非线性光学技术的组合监测。最后,各种CPs的分子结构与聚集类型相关,提供了CPs的分子结构与其ECD之间的一般关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Linking the Chiral Expression of Conjugated Polymers to Their Aggregation Type

Linking the Chiral Expression of Conjugated Polymers to Their Aggregation Type

Due to their strong absorption of visible light, chirality in chiral conjugated polymers (CPs) is typically expressed by electronic circular dichroism (ECD). Unfortunately, while many chiral CPs give rise to strong ECD upon stacking, predicting and reproducing the resulting behavior has proven to be extremely difficult. Here we show that the ECD of CPs is correlated to the known types I and II aggregation. It is demonstrated that type I aggregation results in an ECD signal with an additional monosignal Cotton effect, therefore yielding an asymmetrical spectrum. In contrast, in type II aggregation, the resulting ECD signal is symmetrical. This is determined for a model chiral CP, poly(3-(3,7-(S)-dimethyloctyl)thiophene) in two ways. Additionally, the actual process of both aggregation types is monitored by a combination of linear and nonlinear optical techniques. Finally, the molecular structure of various CPs is correlated to the aggregation type, providing a general relationship between the molecular structure of CPs and their ECD.

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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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