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线性树枝状两嵌段共聚物的自组装:从纳米纤维到聚合物囊泡。

Self-assembly of linear-dendritic diblock copolymers: from nanofibers to polymersomes.

机构信息

Departamento de Química Orgánica y Química Física, Facultad de Ciencias-Instituto de Ciencia de Materiales de Aragón, Universidad de Zaragoza-CSIC, 50009 Zaragoza, Spain.

出版信息

J Am Chem Soc. 2010 Mar 24;132(11):3762-9. doi: 10.1021/ja9083946.

Abstract

We report the formation of cylindrical micelles, sheet-like micelles, tubular micelles, as well as polymer vesicles by a new series of amphiphilic linear-dendritic block-copolymers (BCs). The BCs, noted as PEGm-AZOn, are composed of poly(ethylene glycol) (PEG) chains of different molecular weights as hydrophilic blocks and the first four generations of azobenzene-containing dendrons based on 2,2-bis(hydroxymethyl)propionic acid (bis-MPA) as hydrophobic blocks (m represents the degree of polymerization of PEG, and n is the number of azobenzene units at the periphery of dendron). The polymeric aggregates were formed by adding water to solutions of the BCs in dioxane. The micellar dispersions in water were finally obtained by removing dioxane via dialysis against water. The morphology of the micellar self-assemblies was studied by transmission electron microscopy (TEM), cryo-electron microscopy (cryo-TEM), and atomic force microscopy (AFM). A generation-dependent aggregation behavior was found for the series of BCs PEG45-AZOn. Core-shell structured nanofibers with an inner diameter of 8 nm were observed for the copolymer PEG45-AZO2 (hydrophilic/hydrophobic weight ratio equal to 67/33). Lyotropic liquid crystalline behavior was detected for the aqueous solution of the nanofibers. The coexistence of sheet-like aggregates and tubular micelles was detected for the copolymer PEG45-AZO8 in which the number of cyanoazobenzene units is increased to 8 (hydrophilic/hydrophobic weight ratio equal to 33/67). The tubular micelles could be intermediates in the sheet-like aggregate-to-vesicle transition. Polymer vesicles (polymersomes) with a diameter in the range 300-800 nm were observed for the copolymer PEG45-AZO16 (hydrophilic/hydrophobic weight ratio equal to 20/80). The membrane of the sheet-like aggregates, tubular micelles, and polymersomes was shown to have a bilayer structure, as revealed by cryo-TEM. UV illumination of the aqueous polymersome dispersion induced the formation of wrinkles in the vesicle membrane, thus showing that this type of polymeric aggregate is photoresponsive.

摘要

我们报告了由一系列新型两亲性线性-树枝状嵌段共聚物(BCs)形成的圆柱形胶束、片状胶束、管状胶束以及聚合物囊泡。这些被标记为 PEGm-AZOn 的 BCs 由不同分子量的聚乙二醇(PEG)链作为亲水嵌段和基于 2,2-双(羟甲基)丙酸(bis-MPA)的第一代到第四代含偶氮苯的树枝状大分子作为疏水嵌段组成(m 代表 PEG 的聚合度,n 是树枝状大分子外围偶氮苯单元的数量)。通过在二氧六环中添加水,形成了聚合物的聚集体。通过透析将二氧六环除去,最终得到水相中的胶束分散体。通过透射电子显微镜(TEM)、冷冻电子显微镜(cryo-TEM)和原子力显微镜(AFM)研究了胶束自组装的形态。我们发现了这一系列 BCsPEG45-AZOn 的与代相关的聚集行为。共聚物 PEG45-AZO2(亲/疏水性重量比等于 67/33)观察到具有 8nm 内径的核壳结构纳米纤维。检测到纳米纤维水溶液的溶致液晶行为。对于共聚物 PEG45-AZO8,当氰基偶氮苯单元的数量增加到 8 时(亲/疏水性重量比等于 33/67),检测到片状聚集体和管状胶束的共存。管状胶束可能是片状聚集体到囊泡转变的中间体。对于共聚物 PEG45-AZO16(亲/疏水性重量比等于 20/80),观察到直径在 300-800nm 范围内的聚合物囊泡(聚合物囊泡)。通过 cryo-TEM 揭示,片状聚集体、管状胶束和聚合物囊泡的膜具有双层结构。水相聚合物囊泡分散体的紫外光照射诱导囊泡膜形成皱纹,表明这种类型的聚合物聚集体具有光响应性。

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