双吡咯烷酮结构作为合成生物基聚酯和制备添加剂的通用构件。

IF 9.3 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Green Chemistry Pub Date : 2025-01-03 DOI:10.1039/d4gc04951a
Nele Schulte, Giacomo Damonte, Valeria Marisa Rocca, Anamaria Todea, Orietta Monticelli, Alessandro Pellis
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引用次数: 0

摘要

本研究将衣康酸的二甲酯衍生物衣康酸二甲酯(DMI)与碳链长度为C4至C12的脂肪族二胺结合,合成了三种双吡咯烷酮基结构(BP),目的是开发新的生物基构建模块。所有三种bp的纯度都达到了约93%,无需进行任何繁琐的纯化步骤即可进一步使用,因此可以轻松地在10克规模上进行合成。它们的潜在应用在现代高分子科学的两个关键领域得到了证明:(1)酶促合成聚酯和(2)用作聚乳酸(PLA)添加剂。首先,由于酶催化的使用,在无溶剂反应体系中,BP单体与各种脂肪二醇反应获得低聚酯的可能性得到了证明。线性低聚酯的平均分子量在1000 g mol-1和6100 g mol-1之间,在聚酯基体中的分散值为-1 BP,与整齐的聚合物基体相比,其断裂伸长率提高了8倍,玻璃化转变温度降低了。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bis-pyrrolidone structures as versatile building blocks for the synthesis of bio-based polyesters and for the preparation of additives.

In this work, three bis-pyrrolidone-based structures (BP) were synthesized combining dimethyl itaconate (DMI), the dimethyl ester derivative of itaconic acid, with various aliphatic diamines having a C4 to C12 carbon chain length with the aim of developing novel bio-based building blocks. All three BPs were obtained with a purity >93% and could further be used without performing any tedious purification step, therefore allowing an easy scalability of the synthesis on a 10 g scale. Their potential application was demonstrated in two key areas of modern polymer science: (1) the enzymatic synthesis of polyesters and (2) their use as poly(lactic acid) (PLA) additives. Firstly, the possibility of obtaining oligoesters by reacting the BP monomers with various aliphatic diols in a solventless reaction system and under mild conditions (T < 90 °C) was demonstrated thanks to the use of enzymatic catalysis. Linear oligoesters having mean average molecular weights between 1000 g mol-1 and 6100 g mol-1 and dispersity values <2 were successfully obtained. When applying the BP structures as PLA additives, the incorporation of a 10% w w-1 BP in the polyester matrix resulted in systems with an 8× increased elongation at break and a decrease in the glass transition temperature compared to the neat polymer matrix.

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来源期刊
Green Chemistry
Green Chemistry 化学-化学综合
CiteScore
16.10
自引率
7.10%
发文量
677
审稿时长
1.4 months
期刊介绍: Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.
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