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Preparation and Cross-Linking of All-Acrylamide Diblock Copolymer Nano-Objects via Polymerization-Induced Self-Assembly in Aqueous Solution

机译:通过聚合诱导的水溶液中的丙烯酰胺二嵌段共聚物纳米物体的制备与交联

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摘要

Various carboxylic acid-functionalized poly( N , N -dimethylacrylamide) (PDMAC) macromolecular chain transfer agents (macro-CTAs) were chain-extended with diacetone acrylamide (DAAM) by reversible addition-fragmentation chain transfer (RAFT) aqueous dispersion polymerization at 70 °C and 20% w/w solids to produce a series of PDMAC-PDAAM diblock copolymer nano-objects via polymerization-induced self-assembly (PISA). TEM studies indicate that a PDMAC macro-CTA with a mean degree of polymerization (DP) of 68 or higher results in the formation of well-defined spherical nanoparticles with mean diameters ranging from 40 to 150 nm. In contrast, either highly anisotropic worms or polydisperse vesicles are formed when relatively short macro-CTAs (DP = 40-58) are used. A phase diagram was constructed to enable accurate targeting of pure copolymer morphologies. Dynamic light scattering (DLS) and aqueous electrophoresis studies indicated that in most cases these PDMAC-PDAAM nano-objects are surprisingly resistant to changes in either solution pH or temperature. However, PDMAC40-PDAAM99 worms do undergo partial dissociation to form a mixture of relatively short worms and spheres on adjusting the solution pH from pH 2-3 to around pH 9 at 20 °C. Moreover, a change in copolymer morphology from worms to a mixture of short worms and vesicles was observed by DLS and TEM on heating this worm dispersion to 50 °C. Postpolymerization cross-linking of concentrated aqueous dispersions of PDMAC-PDAAM spheres, worms, or vesicles was performed at ambient temperature using adipic acid dihydrazide (ADH), which reacts with the hydrophobic ketone-functionalized PDAAM chains. The formation of hydrazone groups was monitored by FT-IR spectroscopy and afforded covalently stabilized nano-objects that remained intact on exposure to methanol, which is a good solvent for both blocks. Rheological studies indicated that the cross-linked worms formed a stronger gel compared to linear precursor worms.
机译:在70℃下,通过可逆加成-断裂链转移(RAFT)水分散聚合,用双丙酮丙烯酰胺(DAAM)对各种羧酸官能化的聚(N,N-二甲基丙烯酰胺)(PDMAC)大分子链转移剂(macro-CTA)进行扩链。 °C和20%w / w的固体通过聚合诱导自组装(PISA)来生产一系列PDMAC-PDAAM二嵌段共聚物纳米物体。 TEM研究表明,平均聚合度(DP)为68或更高的PDMAC宏观CTA导致形成平均直径范围为40至150 nm的轮廓分明的球形纳米颗粒。相反,当使用相对较短的宏CTA(DP = 40-58)时,会形成高度各向异性的蠕虫或多分散的囊泡。构造了一个相图,可以精确靶向纯共聚物形态。动态光散射(DLS)和水性电泳研究表明,在大多数情况下,这些PDMAC-PDAAM纳米物体令人惊讶地耐受溶液pH或温度的变化。但是,在将溶液的pH值从2-3调节到20°C时,PDMAC40-PDAAM99蠕虫确实会发生部分解离以形成相对较短的蠕虫和球体的混合物。此外,在将这种蠕虫分散体加热至50°C时,通过DLS和TEM观察到共聚物形态从蠕虫变为短蠕虫和囊泡的混合物。使用己二酸二酰肼(ADH)在室温下进行PDMAC-PDAAM球体,蠕虫或囊泡浓缩水分散体的后聚合交联,该己二酸与疏水性酮官能化的PDAAM链反应。基团的形成通过FT-IR光谱法进行监测,并提供了共价稳定的纳米物体,当暴露于甲醇时,该物体仍然完好无损,而甲醇对于这两种嵌段都是很好的溶剂。流变学研究表明,与线性前驱蠕虫相比,交联蠕虫形成了更强的凝胶。

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