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通过同步聚合、结晶和自组装制备可扩展且均匀的 1D 纳米粒子。

Scalable and uniform 1D nanoparticles by synchronous polymerization, crystallization and self-assembly.

机构信息

School of Chemistry, University of Bristol, Cantock's Close, Bristol BS8 1TS, UK.

出版信息

Nat Chem. 2017 Aug;9(8):785-792. doi: 10.1038/nchem.2721. Epub 2017 Feb 13.

Abstract

The preparation of well-defined nanoparticles based on soft matter, using solution-processing techniques on a commercially viable scale, is a major challenge of widespread importance. Self-assembly of block copolymers in solvents that selectively solvate one of the segments provides a promising route to core-corona nanoparticles (micelles) with a wide range of potential uses. Nevertheless, significant limitations to this approach also exist. For example, the solution processing of block copolymers generally follows a separate synthesis step and is normally performed at high dilution. Moreover, non-spherical micelles-which are promising for many applications-are generally difficult to access, samples are polydisperse and precise dimensional control is not possible. Here we demonstrate the formation of platelet and cylindrical micelles at concentrations up to 25% solids via a one-pot approach-starting from monomers-that combines polymerization-induced and crystallization-driven self-assembly. We also show that performing the procedure in the presence of small seed micelles allows the scalable formation of low dispersity samples of cylindrical micelles of controlled length up to three micrometres.

摘要

基于软物质,采用商业化可行规模的溶液处理技术来制备具有明确结构的纳米颗粒,这是一个具有广泛重要意义的主要挑战。在选择性溶解其中一个链段的溶剂中,嵌段共聚物的自组装为核-壳纳米颗粒(胶束)提供了一条很有前途的途径,具有广泛的潜在用途。然而,这种方法也存在着显著的局限性。例如,嵌段共聚物的溶液处理通常遵循单独的合成步骤,并且通常在高稀释度下进行。此外,非球形胶束——对于许多应用来说很有前景——通常难以获得,样品多分散性较大,并且无法进行精确的尺寸控制。在这里,我们通过一种一锅法(从单体开始)演示了在高达 25%固含量下形成板状和圆柱状胶束,该方法结合了聚合诱导和结晶驱动的自组装。我们还表明,在小种子胶束存在的情况下进行该过程,允许可规模化制备具有低分散性的、长度可控至 3 微米的圆柱状胶束样品。

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