Aziridine-Based Organocatalytic Polymerization for Tunable Sulfur Incorporation in Polyureas

IF 4.1 2区 化学 Q2 POLYMER SCIENCE
Leying Xu, Changzheng Ju, Jiazi Zheng, Qingyong Chen, Zhen Zhang
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引用次数: 0

Abstract

Developing new methods for converting inorganic sulfur into sulfur-containing polymers is crucial for advancing both sustainable development and innovative polymeric materials. In this study, we present an aziridine-based polymerization strategy to synthesize polyureas with tunable sulfur incorporation. The process begins with the reaction of aziridine with isocyanate, followed by a ring-opening reaction with an inorganic sulfur reagent. When elemental sulfur is used, oligosulfide anions form in the presence of an organobase, which then nucleophilically attack the aziridine ring, producing oligosulfide-functionalized polyureas. Alternatively, using sodium sulfide generates poly(thioether urea)s through a similar ring-opening mechanism. Model reactions confirm successful sulfur incorporation during these processes. Additionally, a cross-linked polyurea synthesized with tri-isocyanate exhibits excellent mechanical properties, with tensile stress exceeding 30 MPa, and demonstrates good reprocessability due to the dynamic nature of the oligosulfide bonds. Overall, this polymerization approach broadens the range of sulfur-containing materials and supports further advances in aziridine-based polymer chemistry.
基于叠氮吡啶的可调硫合成聚氨酯的有机催化聚合
开发将无机硫转化为含硫聚合物的新方法对于推进可持续发展和创新聚合物材料至关重要。在这项研究中,我们提出了一种基于叠氮吡啶的聚合策略来合成含硫可调的聚氨酯。该工艺以叠氮吡啶与异氰酸酯的反应开始,然后与无机硫试剂进行开环反应。当使用单质硫时,低硫阴离子在有机碱的存在下形成,然后亲核攻击氮吡啶环,产生低硫功能化聚氨酯。或者,使用硫化钠通过类似的开环机制生成聚硫醚尿素。模型反应证实在这些过程中硫的成功掺入。此外,由三异氰酸酯合成的交联聚脲具有优异的力学性能,拉伸应力超过30 MPa,并且由于低聚硫键的动态性质而表现出良好的再加工性能。总的来说,这种聚合方法拓宽了含硫材料的范围,并支持了氮吡啶基聚合物化学的进一步发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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