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Non-Centrosymmetric Cylindrical Micelles by Unidirectional Growth

机译:非中心对称圆柱状胶束的单向生长

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摘要

Although solution self-assembly of block copolymers (BCPs) represents one of the most promising approaches to the creation of nanoparticles from soft matter, the formation of non-centrosymmetric nanostructures with shape anisotropy remains a major challenge. Through a combination of crystallization-driven self-assembly of crystalline-coil BCPs in solution and selective micelle corona cross-linking, we have created short (about 130 nanometers), monodisperse cylindrical seed micelles that grow unidirectionally. These nanostructures grow to form long, non-centrosymmetric cylindrical A-B and A-B-C block co-micelles upon the addition of further BCPs. We also illustrate the formation of amphiphilic cylindrical A-B-C block co-micelles, which spontaneously self-assemble into hierarchical star-shaped supermicelle architectures with a diameter of about 3 micrometers. The method described enables the rational creation of non-centrosymmetric, high aspect ratio, colloidally stable core-shell nanoparticles in a manner that until now has been restricted to the biological domain.
机译:尽管嵌段共聚物(BCP)的溶液自组装代表了从软物质中制备纳米颗粒的最有前途的方法之一,但具有形状各向异性的非中心对称纳米结构的形成仍然是主要挑战。通过将结晶驱动的BCP在溶液中的结晶驱动自组装与选择性的胶束电晕交联相结合,我们创造了短的(约130纳米),单分散的圆柱状种子胶束。在添加其他BCP时,这些纳米结构生长形成长的,非中心对称的圆柱形A-B和A-B-C嵌段胶束。我们还说明了两亲圆柱形A-B-C嵌段胶束的形成,该胶束自发地自组装成直径约为3微米的分层星形胶束结构。所描述的方法能够以迄今仅限于生物学领域的方式合理地产生非中心对称的,高长宽比的,胶体稳定的核-壳纳米颗粒。

著录项

  • 来源
    《Science》 |2012年第6094期|p.559-562|共4页
  • 作者单位

    School of Chemistry, University of Bristol, Bristol BS8 1TS, UK;

    School of Chemistry, University of Bristol, Bristol BS8 1TS, UK;

    Department of Chemistry, University of Toronto, Toronto, Ontario M5S 3H6, Canada;

    School of Chemistry, University of Bristol, Bristol BS8 1TS, UK;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-18 02:53:34

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