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无硫自由基 RAFT 聚合甲基丙烯酸酯均相溶液:外向烯烃链转移剂(R-CH=C(=CH )Z)的设计。

Sulfur-Free Radical RAFT Polymerization of Methacrylates in Homogeneous Solution: Design of exo-Olefin Chain-Transfer Agents (R-CH C(=CH )Z).

机构信息

Department of Molecular and Macromolecular Chemistry, Graduate School of Engineering, Nagoya University Furo-cho, Chikusa-ku, Nagoya, 464-8603, Japan.

Department of Chemical Science and Engineering, School of Materials and Chemical Technology, Tokyo Institute of Technology, 2-12-1-H120 Ookayama, Meguro-ku, Tokyo, 152-8550, Japan.

出版信息

Angew Chem Int Ed Engl. 2022 Dec 23;61(52):e202212633. doi: 10.1002/anie.202212633. Epub 2022 Nov 23.

Abstract

In this work, the development of exo-olefin compounds (R-CH C(=CH )Z) as chain-transfer agents for the sulfur-free reversible addition-fragmentation chain transfer (RAFT) radical polymerization of methacrylates in homogeneous solution is described. A series of exo-olefin compounds with a methyl methacrylate (MMA) dimer structure as the R group and a substituted α-methylstyrene unit as the -CH C(=CH )Z (Z: Ph-Y) group were synthesized and used for the radical polymerization of MMA in toluene and PhC(CF ) OH. These compounds underwent transfer of the CH C(=CH )Z group via addition-fragmentation of the propagating methacryloyl radical. More electron-donating (Y) substituents, such as methoxy and dimethylamino groups, produced polymers with narrower molecular weight distributions. A continuous monomer addition method further improved molecular weight control and enabled the synthesis of colorless, sulfur-free, multiblock copolymers of methacrylates in homogeneous solutions.

摘要

在这项工作中,开发了外烯烃化合物(R-CH=C(=CH )Z)作为链转移剂,用于在均相溶液中无硫的可逆加成-断裂链转移(RAFT)自由基聚合甲基丙烯酸酯。一系列具有甲基丙烯酸甲酯(MMA)二聚体结构作为 R 基团和取代的α-甲基苯乙烯单元作为-CH=C(=CH )Z(Z:Ph-Y)基团的外烯烃化合物被合成,并用于 MMA 在甲苯和 PhC(CF )OH 中的自由基聚合。这些化合物通过增长的丙烯酰基自由基的加成-断裂进行 CH=C(=CH )Z 基团的转移。更多供电子(Y)取代基,如甲氧基和二甲氨基,产生了具有更窄分子量分布的聚合物。连续单体添加方法进一步改善了分子量控制,并能够在均相溶液中合成无色、无硫的多嵌段甲基丙烯酸酯共聚物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b54/10099145/e6d7aca3977f/ANIE-61-0-g006.jpg

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