1.南京工业大学,生物与制药工程学院 材料化学工程国家重点实验室,南京 211800
2.南京工业大学,材料科学与工程学院,南京 211800
E-mail: xinhu@njtech.edu.cn;
E-mail: ningzhu@njtech.edu.cn
收稿:2026-01-15,
录用:2026-03-12,
网络首发:2026-04-07,
移动端阅览
徐婷婷, 李牧舟, 胡欣, 朱宁. 开环易位聚合诱导自组装. 高分子学报, doi: 10.11777/j.issn1000-3304.2026.26009.
Xu, T. T.; Li, M. Z.; Hu, X.; Zhu, N. Ring-opening metathesis polymerization-induced self-assembly. Acta Polymerica Sinica (in Chinese), doi: 10.11777/j.issn1000-3304.2026.26009.
徐婷婷, 李牧舟, 胡欣, 朱宁. 开环易位聚合诱导自组装. 高分子学报, doi: 10.11777/j.issn1000-3304.2026.26009. DOI: CSTR: 32057.14.GFZXB.2026.7574.
Xu, T. T.; Li, M. Z.; Hu, X.; Zhu, N. Ring-opening metathesis polymerization-induced self-assembly. Acta Polymerica Sinica (in Chinese), doi: 10.11777/j.issn1000-3304.2026.26009. DOI: CSTR: 32057.14.GFZXB.2026.7574.
聚合诱导自组装(PISA)已成为一种高效合成固含量高、形貌多样纳米颗粒的新方法,在高分子化学和纳米材料等领域引起了广泛关注. 近年来,面向环烯烃单体的开环易位聚合(ROMP)具有可控性好、官能团耐受性高、适配大位阻单体等优势,越来越多地应用于聚合诱导自组装领域,成功获得系列主链含有不饱和双键的聚合物纳米颗粒. 本综述聚焦开环易位聚合诱导自组装(ROMPISA),从有机相、水相和有机/水相三个方面,总结开环易位聚合诱导自组装在纳米颗粒形貌控制、功能调控以及应用等方面的研究进展,同时探讨了相关领域存在的机遇与挑战,希望为聚合诱导自组装领域的发展提供借鉴.
Polymerization-induced self-assembly (PISA) has emerged as a highly efficient strategy for the synthesis of high-solid-content nano-objects with diverse morphologies
which has attracted growing interest in polymer chemistry and nanomaterials. In recent years
the ring-opening metathesis polymerization (ROMP) of cyclic olefin monomers has been used in PISA because of its good controllability
high tolerance for functional groups
and availability for sterically hindered monomers. Ring-opening metathesis polymerization-induced self-assembly (ROMPISA) has been demonstrated as a powerful platform for the preparation of a series of polyolefin block copolymer nano-objects containing unsaturated double bonds in the main chain. This review focuses on the advances in ring-opening metathesis polymerization-induced self-assembly. The morphologies
functions
and applications of nano-objects from ROMPISA are summarized from the perspectives of the organic
aqueous
and organic/aqueous phases
respectively. Challenges and opportunities are discussed to provide insights into the further development of polymerization-induced self-assembly.
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