脂环化合物
化学
有机化学
高分子科学
高分子化学
材料科学
解聚
聚合物
预聚物
反应机理
作者
Yue Wang,Mengwei Du,Ting Xu,Fenghuan Yang,Mingfa Guo,Ruimin Xie,Rongliang Wu,H P Wang,J Wu
出处
期刊:Macromolecules
[American Chemical Society]
日期:2026-05-21
卷期号:59 (11): 6209-6222
标识
DOI:10.1021/acs.macromol.6c00184
摘要
To advance the development of sustainable high-performance polycarbonates, a series of novel copolycarbonates (PITCs) were designed and synthesized using two biobased alicyclic building blocks: isosorbide (IS) and 2,5-tetrahydrofurandimethanol (THFDM). The target polycarbonates were prepared via melt polymerization, yielding materials with number-average molecular weights ranging from 51,600 to 75,500 g/mol. By integrating density functional theory calculations with kinetic studies, we elucidated the reaction mechanism and monomer reactivity, confirming that intermolecular interactions between the building blocks promote polymerization efficiency. Notably, the incorporation of THFDM significantly enhanced the cohesive energy density of the PITC matrix, enabling PI 89 T 11 C and PI 70 T 30 C to achieve balanced performance: high glass transition temperatures ( T g ) of 151.2 °C and 115.8 °C, respectively, superior tensile strength (74–75 MPa), and excellent elongation at break (70–92%). In contrast, PITCs with high THFDM content (≥90 mol %) exhibited exceptional flexibility, with elongation at break values ranging from 900% to 1600%. Additionally, all PITCs maintained high transparency (∼93% light transmittance) and elevated biobased content (82–84%). These biobased, high-performance copolycarbonates thus hold significant promise for the development of eco-friendly and sustainable advanced engineering materials.
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