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增塑剂诱导的不同链长手性聚合物薄膜中细观不对称性增强

Plasticizer-Induced Enhancement of Mesoscale Dissymmetry in Thin Films of Chiral Polymers with Variable Chain Length.

作者信息

Joseph Jojo P, Malone Trent, Abraham Shema R, Dutta Avisek, Gupta Sonal, Kuzmin Andrey, Baev Alexander, Swihart Mark T, Hendrickson Joshua R, Prasad Paras N

机构信息

Department of Chemistry and The Institute for Lasers, Photonics, and Biophotonics, University at Buffalo, SUNY, Buffalo, NY, 14260, USA.

Department of Electro-Optics and Photonics, University of Dayton, Dayton, OH, 45469, USA.

出版信息

Adv Mater. 2024 Jan;36(4):e2305684. doi: 10.1002/adma.202305684. Epub 2023 Dec 4.

DOI:10.1002/adma.202305684
PMID:37725635
Abstract

Conjugated polymers with chiral side chains are of interest in areas including chiral photonics, optoelectronics, and chemical and biological sensing. However, the low dissymmetry factors of most neat polymer thin films have limited their practical application. Here, a robust method to increase the absorption dissymmetry factor in a poly-fluorene-thiophene (PF8TS series) system is demonstrated by varying molecular weight and introducing an achiral plasticizer, polyethylene mono alcohol (PEM-OH). Extending chain length within the optimal range and adding this long-chain alcohol significantly enhance the chiroptical properties of spin-coated and annealed thin films. Mueller matrix spectroscopic ellipsometry (MMSE) analysis shows good agreement with the steady-state transmission measurements confirming a strong chiral response (circular dichroism (CD) and circular birefringence (CB)), ruling out linear dichroism, birefringence, and specific reflection effects. Solid-state NMR studies of annealed hybrid chiral polymer systems show enhancement of signals associated with aromatic π-stacked backbone and the ordered side-chain conformations. Further studies using Raman spectroscopy, X-ray diffraction (XRD), differential scanning calorimetry (DSC), atomic force microscopy (AFM), and polarized optical microscopy (POM) indicate that PEM-OH facilitates mesoscopic crystal domain ordering upon annealing. This provides new insights into routes for tuning optical activity in conjugated polymers.

摘要

具有手性侧链的共轭聚合物在手性光子学、光电子学以及化学和生物传感等领域备受关注。然而,大多数纯聚合物薄膜的低不对称因子限制了它们的实际应用。在此,通过改变分子量并引入非手性增塑剂聚乙烯单醇(PEM-OH),展示了一种在聚芴-噻吩(PF8TS系列)体系中提高吸收不对称因子的稳健方法。在最佳范围内延长链长并添加这种长链醇可显著增强旋涂和退火薄膜的手性光学性质。穆勒矩阵光谱椭偏仪(MMSE)分析与稳态透射测量结果吻合良好,证实了强烈的手性响应(圆二色性(CD)和圆双折射(CB)),排除了线性二色性、双折射和特定反射效应。对退火后的混合手性聚合物体系进行的固态核磁共振研究表明,与芳香族π堆积主链和有序侧链构象相关的信号增强。使用拉曼光谱、X射线衍射(XRD)、差示扫描量热法(DSC)、原子力显微镜(AFM)和偏振光学显微镜(POM)进行的进一步研究表明,PEM-OH在退火时促进介观晶畴有序化。这为调节共轭聚合物光学活性的途径提供了新的见解。

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