一锅制备聚合驱动的非常规发光聚合物凝胶

IF 3.9 2区 化学 Q2 POLYMER SCIENCE
Nan Jiang , Xin Pu , Ke-Xin Li , Chang-Yi Zhu , Yu-Wei Sun , Yan-Hong Xu , You-Liang Zhu , Martin R. Bryce
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引用次数: 0

摘要

非常规发色团是制备发光凝胶的良好候选材料,因为它们的发光通常在聚集状态下会增强。本研究开发了一种简单的聚合物荧光凝胶聚合诱导凝胶化的一锅策略,并获得了一种基于非共轭/非常规发光聚氨酯衍生物的自物理交联发光凝胶 PUHG。详细的实验和理论研究探究了 PUHG 聚合态的物理性质和发光原理。分子动力学模拟表明,聚氨酯链之间丰富的非共价相互作用和物理纠缠是凝胶形成的主要驱动力和发光源。PUHG 显示出稳定的光物理性质、环境耐受性、良好的粘附性和可加工性,从而验证了 PUHG 在不同有机/无机基底上的图案化应用。这项工作拓宽了非常规发光聚合物的应用范围,并为大规模制备荧光凝胶软材料提供了一条简单的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

One-pot preparation of nonconventional luminescent polymer gels driven by polymerization†

One-pot preparation of nonconventional luminescent polymer gels driven by polymerization†

One-pot preparation of nonconventional luminescent polymer gels driven by polymerization†
Nonconventional chromophores are good candidates for preparing luminous gels because their luminescence is usually enhanced in the aggregated state. In this work, a simple one-pot strategy for polymerization-induced gelation of polymer fluorescent gels was developed, and a self physically crosslinked luminous gel PUHG based on a non-conjugated/nonconventional luminous polyurethane derivative was obtained. Detailed experimental and theoretical studies probed the physical properties and luminescence principles of PUHG's aggregated state. Molecular dynamics simulations suggest that abundant non-covalent interactions and physical entanglement between polyurethane chains are the main driving forces of gel formation and the source of luminescence. PUHG displays stable photophysical properties, environmental tolerance, good adhesion properties and processability, leading to the validation of patterning applications of PUHG on different organic/inorganic substrates. This work broadens the application range of nonconventional luminous polymers and provides a simple route for large-scale preparation of fluorescent gel soft materials.
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来源期刊
Polymer Chemistry
Polymer Chemistry POLYMER SCIENCE-
CiteScore
8.60
自引率
8.70%
发文量
535
审稿时长
1.7 months
期刊介绍: Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.
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