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    秦王俊, 雷啸天, 罗 静, 刘 仁, 朱 叶. 氢键辅助光诱导N-乙基马来酰亚胺/甲基丙烯酸甲酯序列可控共聚物的聚合[J]. 功能高分子学报,2023,36(4):372-380. doi: 10.14133/j.cnki.1008-9357.20230406001
    引用本文: 秦王俊, 雷啸天, 罗 静, 刘 仁, 朱 叶. 氢键辅助光诱导N-乙基马来酰亚胺/甲基丙烯酸甲酯序列可控共聚物的聚合[J]. 功能高分子学报,2023,36(4):372-380. doi: 10.14133/j.cnki.1008-9357.20230406001
    QIN Wangjun, LEI Xiaotian, LUO Jing, LIU Ren, ZHU Ye. Hydrogen Bond Driven Photoinduced Sequence Control Polymerization of N-Ethylmaleimide and Methyl Methacrylate[J]. Journal of Functional Polymers, 2023, 36(4): 372-380. doi: 10.14133/j.cnki.1008-9357.20230406001
    Citation: QIN Wangjun, LEI Xiaotian, LUO Jing, LIU Ren, ZHU Ye. Hydrogen Bond Driven Photoinduced Sequence Control Polymerization of N-Ethylmaleimide and Methyl Methacrylate[J]. Journal of Functional Polymers, 2023, 36(4): 372-380. doi: 10.14133/j.cnki.1008-9357.20230406001

    氢键辅助光诱导N-乙基马来酰亚胺/甲基丙烯酸甲酯序列可控共聚物的聚合

    Hydrogen Bond Driven Photoinduced Sequence Control Polymerization of N-Ethylmaleimide and Methyl Methacrylate

    • 摘要: 在405 nm光源辐照下,采用二硫代羰基苯甲酸异丁腈酯(CPDB)作为光引发剂和链转移剂,对N-乙基马来酰亚胺(NEM)和甲基丙烯酸甲酯(MMA)的光诱导链转移共聚行为进行了研究。通过核磁共振氢谱(1H-NMR)和基质辅助激光解吸电离飞行时间质谱(MALDI-TOF-MS)对共聚物的结构进行了表征。利用1,1,1,3,3,3-六氟-2-丙醇(HFP)溶剂与单体构筑氢键,探究了HFP的最佳添加量,并通过单体在聚合物中的累计组成(Fcum)与其在聚合过程中的瞬间组成(Finst)之间的关系,对不同聚合条件下聚合物的组成和序列结构进行了探究。结果表明:在405 nm光照下,CPDB能够成功引发NEM和MMA的共聚,且聚合行为具有活性特征;当HFP与单体的物质的量之比为1∶1时,MMA单体会优先与HFP形成氢键,使NEM和MMA反应速率相近,形成交替结构共聚物;当不以HFP为溶剂或在加热条件下进行聚合时,NEM和MMA共聚得到的共聚物均为梯度共聚物。

       

      Abstract: The photo copolymerization of N-ethylmaleimide (NEM) and methyl methacrylate (MMA) in 1,1,1,3,3,3-hexafluoro-2-propanol (HFP) and dichloromethane (DCM) was reported. The polymerization was carried out by Reversible Addition-Fragmentation Chain Transfer (RAFT) polymerization method using 2-(2-cyanopropyl) dithiobenzoate (CPDB) as the initiation-regulation dual functional agent. The copolymerization behavior of this monomer pair was investigated in detail at different reaction conditions. The structures of the copolymers were characterized by 1H-NMR and MALDI-TOF-MS. Results revealed that fluoroalcohols were quite effective in affording the copolymers with controlled molecular weights and adjustable MMA contents compared with the normal solvent DCM, due to the hydrogen-bonding interaction. When the molar ratio between HFP and monomer was 1∶1, the reaction rate of NEM was similar to that of MMA, and NEM and MMA were written alternately to the polymer chain to form an alternate copolymer with a well-defined sequence structure.

       

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