原子转移自由基聚合
单体
高分子化学
聚合物
凝胶渗透色谱法
聚合
甲基丙烯酰胺
荧光
甲基丙烯酸甲酯
二乙烯基苯
甲基丙烯酸酯
化学
材料科学
共聚物
有机化学
苯乙烯
丙烯酰胺
物理
量子力学
作者
M. Spiniello,Anton Blencowe,Greg G. Qiao
摘要
Abstract A series of fluorescently labeled core cross‐linked star (CCS) polymers were synthesized via the “arm‐first” approach, employing atom transfer radical polymerization (ATRP) to control the resulting architecture. The initiator p ‐toluenesulfonyl chloride (TsCl) was used to synthesize “living” poly(methyl methacrylate) (PMMA) macroinitiator, which was subsequently cross‐linked to generate the CCS polymers. Divinylbenzene (DVB) was used as the cross‐linker and 7‐[4‐(trifluoromethyl)coumarin] methacrylamide ( F 1 , λ ex = 343 nm) was added as a fluorescent labeling monomer. A range of PMMA/DVB/ F 1 based CCS polymers were synthesized with the core domain made selectively fluorescent by using varying amounts of monomer F 1 . The core functionalized stars were characterized using gel permeation chromatography (GPC) equipped with multi‐angle laser light scattering (MALLS), refractive index (RI), and UV–visible detectors. The fluorescence quantum yield (Φ F ) and the amount of fluorescent monomer incorporated into the core were quantified by UV–visible and fluorescence spectrophotometry. It was recognized that the overall molecular weights of the stars produced, along with their core molecular weight, decreased as the mol % of monomer F 1 was increased relative to cross‐linker. Visual confirmation of F 1 incorporation was obtained by fluorescence microscopy of thin polymer films cast on glass substrates. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 2422–2432, 2008
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