链式转移
聚合
共聚物
高分子化学
单体
材料科学
活性聚合
甲基丙烯酸酯
可逆加成-断裂链转移聚合
乙二醇
聚合物
光化学
自由基聚合
两亲性
分散性
光致聚合物
化学
有机化学
复合材料
作者
Ali Bagheri,Jonathan Yeow,Hamidreza Arandiyan,Jiangtao Xu,Cyrille Boyer,May Lim
标识
DOI:10.1002/marc.201600127
摘要
The polymerization of the photocleavable monomer, o-nitrobenzyl methacrylate (NBMA), is investigated using photoinduced electron/energy transfer reversible addition-fragmentation chain transfer polymerization. The polymerizations under visible red (λ max = 635 nm, 0.7 mW cm(-2) ) and yellow (λ max = 560 nm, 9.7 mW cm(-2) ) light are performed and demonstrate rational evidence of a controlled/living radical polymerization process. Well-defined poly(o-nitrobenzyl methacrylate) (PNBMA) homopolymers with good control over the molecular weight and polymer dispersity are successfully synthesized by varying the irradiation time and/or targeted degree of polymerization. Chain extension of a poly(oligo(ethylene glycol) methyl ether methacrylate) macro-chain transfer agent with NBMA is carried out to fabricate photocleavable amphiphilic block copolymers (BCP). Finally, these self-assembled BCP rapidly dissemble under UV light suggesting the photoresponsive character of NBMA is not altered during the polymerization under yellow or red light. Such photoresponsive polymers can be potentially used for the remote-controlled delivery of therapeutic compounds.
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