封面专题:探索丙烯酸作为氧烷亲核试剂:直接获得聚(β-羟基丙烯酸酯)(ChemSusChem 18/2025)

IF 6.6 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ChemSusChem Pub Date : 2025-09-23 DOI:10.1002/cssc.70133
Céline Montanari, Lukas Marcos Celada, Wenhao Zhang, Peter Olsén
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引用次数: 0

摘要

覆盖特征显示了丙烯酸的开环丙烯酸化,这使得通过与氧烷(环氧化物)直接反应生成β-羟基丙烯酸酯成为一种可扩展的、高收率的途径。这种简单的、原子经济的工艺产生了透明、热稳定的聚合物单体,具有可调的机械性能,从柔软和可拉伸到坚硬和坚固。这项工作突出了丙烯酸在下一代可持续材料中的潜力。更多信息可以在P. Olsen及其同事的研究文章中找到(DOI: 10.1002/cssc.202500575)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cover Feature: Exploring Acrylic Acid as an Oxirane Nucleophile: Direct Access to Poly(β-Hydroxy Acrylates) (ChemSusChem 18/2025)

Cover Feature: Exploring Acrylic Acid as an Oxirane Nucleophile: Direct Access to Poly(β-Hydroxy Acrylates) (ChemSusChem 18/2025)

The Cover Feature shows ring-opening acrylation with acrylic acid, which enables a scalable, high-yield route to β-hydroxy acrylates via direct reaction with oxiranes (epoxides). This simple, atom-economic process yields monomers for transparent, thermally stable polymers with tunable mechanical properties, ranging from soft and stretchable to stiff and strong. The work highlights the potential of acrylic acid in next-generation sustainable materials. More information can be found in the Research Article by P. Olsen and co-workers (DOI: 10.1002/cssc.202500575).

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来源期刊
ChemSusChem
ChemSusChem 化学-化学综合
CiteScore
15.80
自引率
4.80%
发文量
555
审稿时长
1.8 months
期刊介绍: ChemSusChem Impact Factor (2016): 7.226 Scope: Interdisciplinary journal Focuses on research at the interface of chemistry and sustainability Features the best research on sustainability and energy Areas Covered: Chemistry Materials Science Chemical Engineering Biotechnology
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