Synthesis and Postfunctionalization of Acrylate-Appended Poly(cyclohexene carbonate)s: Modulation of Properties of CO2-Based Polymers

IF 5.2 1区 化学 Q1 POLYMER SCIENCE Macromolecules Pub Date : 2025-02-03 DOI:10.1021/acs.macromol.4c02881
Chihiro Maeda, Hina Inoue, Tadashi Ema
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Abstract

Functional CO2-based polycarbonates are expected to be sustainable materials. Herein, a bifunctional aluminum porphyrin catalyzed the terpolymerization of cyclohexene oxide (CHO), acrylate-appended CHO, and CO2 to provide poly(cyclohexene carbonate)s (PCHCs) with acrylate groups. Postfunctionalization of PCHCs via Michael addition or Heck reaction enabled the incorporation of thiol, amine, and aromatics into PCHCs with high selectivity and efficiency. PCHCs with the flexible long alkyl chains showed a glass-transition temperature (Tg) of down to 52 °C, which was much lower than that of PCHC (127 °C). In sharp contrast, PCHCs with rigid pyrenyl groups showed Tg values of up to 152 °C and fluorescence emission. Thus, a wide range of polymers were obtained by robust and sustainable synthetic methods, and the functional groups modulated the properties of the CO2-based polycarbonates.

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含丙烯酸酯的聚碳酸环己烯的合成与后功能化:co2基聚合物性能的调节
功能性二氧化碳基聚碳酸酯有望成为可持续发展的材料。本研究中,双官能团卟啉铝催化氧化环己烯(CHO)、丙烯酸酯-附加CHO和CO2的三元聚合,得到具有丙烯酸酯基团的聚碳酸环己烯(PCHCs)。通过Michael加成或Heck反应对PCHCs进行后官能化,使得硫醇、胺和芳烃以高选择性和高效率结合到PCHCs中。具有柔性长烷基链的PCHC的玻璃化转变温度(Tg)低至52℃,远低于PCHC的127℃。与此形成鲜明对比的是,具有刚性芘基的PCHCs的Tg值高达152°C,并具有荧光发射。因此,通过稳健和可持续的合成方法获得了广泛的聚合物,并且官能团调节了co2基聚碳酸酯的性能。
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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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