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基于狄尔斯-阿尔德化学的“潜在”引发转移终止剂策略一锅法结构可控合成超支化聚合物

One-Pot Structure-Controlled Synthesis of Hyperbranched Polymers by a "Latent" Inimer Strategy Based on Diels-Alder Chemistry.

作者信息

Yang Neng, Jiang Yu, Tan Qinwen, Ma Jiahui, Zhan Dezhi, Wang Zhaohong, Wang Xin, Zhang Daohong, Hadjichristidis Nikos

机构信息

Key Laboratory of Catalysis and Energy Materials Chemistry of Ministry of Education & Hubei Key Laboratory of Catalysis and Materials Science, Hubei R&D Center of Hyperbranched Polymers Synthesis and Applications, South-Central Minzu University, Wuhan, 430074, P. R. China.

Polymer Synthesis Laboratory, KAUST Catalysis Center, Physical Sciences and Engineering Division, King Abdullah University of Science and Technology (KAUST), Thuwal, 23955, Saudi Arabia.

出版信息

Angew Chem Int Ed Engl. 2022 Oct 10;61(41):e202211713. doi: 10.1002/anie.202211713. Epub 2022 Sep 6.

Abstract

An efficient "one-pot" strategy for the structure-controlled synthesis of hyperbranched polymers (HBPs) based on a "latent" inimer (LI-Br), containing a furan-protected maleimide monomer and a haloalkane initiator, is presented. At high temperatures, the "latent" inimer is converted to a "real" inimer after releasing maleimide (MI) via a retro-Diels-Alder (r-DA) reaction and then copolymerized with methyl methacrylate by self-condensing vinyl copolymerization. Due to the dynamic characteristic of the r-DA reaction, the release of naked MI and the subsequent copolymerization can be regulated by the temperature or stereochemistry of Diels-Alder (DA) adducts. Thus, the "one-pot" structure-controlled synthesis of HBPs with various degrees of branching was achieved. By further implementation of a programmable temperature change, some valuable hyperbranched topologies such as star-shaped and long-chain hyperbranched polymers can be constructed avoiding sophisticated synthetic routes.

摘要

本文提出了一种基于“潜在”引发剂(LI-Br)的高效“一锅法”策略,用于结构可控地合成超支化聚合物(HBP),该引发剂包含一个呋喃保护的马来酰亚胺单体和一个卤代烷引发剂。在高温下,“潜在”引发剂通过逆狄尔斯-阿尔德(r-DA)反应释放马来酰亚胺(MI)后转化为“真正的”引发剂,然后通过自缩合乙烯基共聚与甲基丙烯酸甲酯共聚。由于r-DA反应的动态特性,裸MI的释放和随后的共聚可通过狄尔斯-阿尔德(DA)加合物的温度或立体化学来调节。因此,实现了具有不同支化度的HBP的“一锅法”结构可控合成。通过进一步实施可编程温度变化,可以构建一些有价值的超支化拓扑结构,如星形和长链超支化聚合物,避免了复杂的合成路线。

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