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用于合成聚异戊二烯-聚苯乙烯嵌段共聚物和无规共聚物的聚合诱导自组装:迈向高分子量与高转化率

Polymerization-Induced Self-Assembly for the Synthesis of Polyisoprene-Polystyrene Block and Random Copolymers: Towards High Molecular Weight and Conversion.

作者信息

Moradi Maryam, Georgopanos Prokopios

机构信息

Helmholtz-Zentrum Hereon, Institute of Membrane Research, Max-Planck-Straße 1, 21502, Geesthacht, Germany.

出版信息

Macromol Rapid Commun. 2025 Feb;46(3):e2400727. doi: 10.1002/marc.202400727. Epub 2024 Oct 26.

DOI:10.1002/marc.202400727
PMID:39461895
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11800055/
Abstract

In this study, reversible addition-fragmentation chain- transfer (RAFT) polymerization combined with the polymerization-induced self-assembly (PISA) technique is used to synthesize polyisoprene (PI)-based block and random copolymers with polystyrene (PS), aiming for high molecular weight and monomer conversion. The focus is to optimize the polymerization conditions to overcome the existing challenge of cross-linking and Diels-Alder reactions during the polymerization of isoprene, which typically constrain the reaction conversion and molecular weight of the final polymers. Using a poly(methacrylic acid) (PMAA) macroRAFT agent synthesized in ethanol at 80 °C, random and block copolymers of PS-PI with a target molecular weight of 50 000 g mole and a high monomer conversion of ≈80% are achieved under optimized conditions in water-emulsion at 35 °C. H nuclear magnetic resonance (NMR) verified the successful synthesis as well as the high content of 1,4 microstructure in polyisoprene. The thermal analysis via differential scanning calorimetry indicated distinct glass transitions for the microphase-separated PI-PS block copolymer, while a single transition for PI-PS random copolymer, indicating no microphase separation. Furthermore, dynamic light scattering analysis together with transmission electron microscopy provided further insight into the self-assembled emulsion nanoparticles of the polymers indicating a particle size in the range 70 to 130 nm.

摘要

在本研究中,可逆加成-断裂链转移(RAFT)聚合与聚合诱导自组装(PISA)技术相结合,用于合成基于聚异戊二烯(PI)与聚苯乙烯(PS)的嵌段共聚物和无规共聚物,目标是实现高分子量和单体转化率。重点是优化聚合条件,以克服异戊二烯聚合过程中存在的交联和狄尔斯-阿尔德反应的挑战,这些反应通常会限制最终聚合物的反应转化率和分子量。使用在80°C乙醇中合成的聚(甲基丙烯酸)(PMAA)大分子RAFT试剂,在35°C水乳液的优化条件下,实现了目标分子量为50000 g/mol且单体转化率约为80%的PS-PI无规共聚物和嵌段共聚物。氢核磁共振(NMR)验证了合成成功以及聚异戊二烯中1,4微结构的高含量。通过差示扫描量热法进行的热分析表明,微相分离的PI-PS嵌段共聚物有明显的玻璃化转变,而PI-PS无规共聚物只有一个转变,表明没有微相分离。此外,动态光散射分析和透射电子显微镜进一步深入了解了聚合物的自组装乳液纳米颗粒,表明粒径在70至130 nm范围内。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eab8/11800055/a1463ef4acf4/MARC-46-2400727-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eab8/11800055/7c2aa4212ee2/MARC-46-2400727-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eab8/11800055/9cc079a3a115/MARC-46-2400727-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eab8/11800055/a047d0a6c1b5/MARC-46-2400727-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eab8/11800055/4c99705dfb8f/MARC-46-2400727-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eab8/11800055/94366336a1c5/MARC-46-2400727-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eab8/11800055/a1463ef4acf4/MARC-46-2400727-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eab8/11800055/7c2aa4212ee2/MARC-46-2400727-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eab8/11800055/9cc079a3a115/MARC-46-2400727-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eab8/11800055/a047d0a6c1b5/MARC-46-2400727-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eab8/11800055/4c99705dfb8f/MARC-46-2400727-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eab8/11800055/94366336a1c5/MARC-46-2400727-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eab8/11800055/a1463ef4acf4/MARC-46-2400727-g003.jpg

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本文引用的文献

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