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Ultrabright fluorescent polymeric nanoparticles made from a new family of BODIPY monomers

机译:由新型BODIPY单体制成的超亮荧光聚合物纳米颗粒

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摘要

Four novel BODIPY derivatives (π-) functionalized by different polymerizable groups, styrene (S), phenyl acrylate (PhA), ethyl methacrylate (EtMA) and ethyl acrylate (EtA) have been synthesized. Following a formerly established one-pot RAFT miniemulsion polymerization process (GrazonMacromol. Rapid Commun. 2011, 32, 699-705), the fluorophores were copolymerized in a controlled way at 2.6 mol % with styrene in water. On the basis of the polymerization-induced self-assembly (PISA) principle, the copolymers assembled during their formation into fluorescent nanoparticles. The distribution of the fluorescent monomers along the polymer backbone was monitored by kinetic studies of the copolymerization reaction. Fluorescent stationary and time-resolved spectroscopy was then performed on both the monomers and the nanoparticles (NPs) and the observed differences are discussed in view of the distribution of the fluorescent monomers in the polymer chain. With two of the novel fluorescent monomers (πS and πPhA), the brightness of the NPs could be significantly improved (by a factor 2) compared to particles comprising the other BODIPY monomers. The obtained particles were 200 to 2000 times brighter than usual quantum dots and 40 to 300 times brighter than most of the fluorescent polymeric nanoparticles reported in the literature.
机译:合成了四种由不同的可聚合基团官能化的新型BODIPY衍生物(π-),即苯乙烯(S),丙烯酸苯酯(PhA),甲基丙烯酸乙酯(EtMA)和丙烯酸乙酯(EtA)。按照先前建立的一锅法RAFT微乳液聚合工艺(GrazonMacromol.Rapid Commun.2011,32,699-705),将荧光团以2.6 mol%的可控方式与水中的苯乙烯共聚。基于聚合诱导的自组装(PISA)原理,共聚物在形成荧光纳米粒子期间会组装。通过共聚反应的动力学研究来监测荧光单体沿着聚合物主链的分布。然后对单体和纳米颗粒(NPs)进行了荧光固定和时间分辨光谱分析,并且鉴于荧光单体在聚合物链中的分布,讨论了观察到的差异。与包含其他BODIPY单体的颗粒相比,使用两种新型荧光单体(πS和πPhA),可以显着提高NP的亮度(提高2倍)。所获得的颗粒比普通量子点的亮度高200至2000倍,比文献中报道的大多数荧光聚合物纳米粒子的亮度高40至300倍。

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