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Preparation of an amphiphilic diblock copolymer composed of polystyrene and hydrophilic alternating copolymer blocks
Polymer Journal ( IF 2.8 ) Pub Date : 2019-10-28 , DOI: 10.1038/s41428-019-0278-0
Maho Ohshio , Yoko Mizoue , Daijiro Shiino , Tatsuya Matsui , Kazuhiro Oda , Shin-ichi Yusa

Generally, conventional free-radical polymerization of an allyl monomer affords low-molecular-weight oligomers. However, since the allyl monomer can form a charge transfer complex with maleic anhydride (MA), in which the former acts as an electron donor and the latter acts as an acceptor, relatively high-molecular-weight alternating copolymers can be obtained via copolymerization of an allyl monomer and MA. In this study, hydrophilic alternating copolymers (P(11EO/MA)m) of methoxy poly(ethylene glycol) allyl ether (11EO) and MA were prepared via reversible addition–fragmentation chain transfer (RAFT)-controlled radical polymerization. The alternating nature of the polymers was confirmed by the consumption of both monomers during polymerization. The MA units in P(11EO/MA)m were hydrolyzed to prepare pendant carboxylic acid group-containing polymers (P(11EO/MH)m). Furthermore, an amphiphilic diblock copolymer (P(11EO/MH)m-PSn) was prepared via RAFT copolymerization of styrene monomer using P(11EO/MH)m as a macro-chain transfer agent. The association behavior of P(11EO/MH)m-PSn in water was also investigated. Hydrophilic alternating copolymers (P(11EO/MA)m) of methoxy poly(ethylene glycol) allyl ether (11EO) and maleic anhydride (MA) were prepared via controlled radical polymerization. The MA units in P(11EO/MA)m were hydrolyzed to prepare pendant carboxylic acid group-containing polymers (P(11EO/MH)m). Furthermore, an amphiphilic diblock copolymer (P(11EO/MH)m-PSn) was prepared via block copolymerization of styrene using P(11EO/MH)m as a macro-chain transfer agent. The association behavior of P(11EO/MH)m-PSn in water was also investigated.

中文翻译:

由聚苯乙烯和亲水交替共聚物嵌段组成的两亲双嵌段共聚物的制备

通常,烯丙基单体的常规自由基聚合提供低分子量低聚物。然而,由于烯丙基单体可以与马来酸酐(MA)形成电荷转移络合物,其中前者作为电子供体,后者作为受体,通过共聚可以得到较高分子量的交替共聚物。烯丙基单体和MA。在这项研究中,通过可逆加成-断裂链转移 (RAFT) 控制的自由基聚合制备了甲氧基聚(乙二醇)烯丙基醚(11EO)和 MA 的亲水交替共聚物(P(11EO/MA)m)。聚合物的交替性质通过聚合过程中两种单体的消耗得到证实。将 P(11EO/MA)m 中的 MA 单元水解以制备含羧酸侧基的聚合物 (P(11EO/MH)m)。此外,使用 P(11EO/MH)m 作为大链转移剂,通过苯乙烯单体的 RAFT 共聚制备了两亲二嵌段共聚物 (P(11EO/MH)m-PSn)。还研究了 P(11EO/MH)m-PSn 在水中的缔合行为。通过受控自由基聚合制备甲氧基聚(乙二醇)烯丙基醚(11EO)和马来酸酐(MA)的亲水交替共聚物(P(11EO/MA)m)。将 P(11EO/MA)m 中的 MA 单元水解以制备含羧酸侧基的聚合物 (P(11EO/MH)m)。此外,使用 P(11EO/MH)m 作为大链转移剂,通过苯乙烯的嵌段共聚制备了两亲二嵌段共聚物 (P(11EO/MH)m-PSn)。
更新日期:2019-10-28
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