Mann Stephen
Centre for Organized Matter Chemistry, School of Chemistry, University of Bristol, Bristol BS8 1TS, UK.
Nat Mater. 2009 Oct;8(10):781-92. doi: 10.1038/nmat2496. Epub 2009 Sep 6.
Understanding how chemically derived processes control the construction and organization of matter across extended and multiple length scales is of growing interest in many areas of materials research. Here we review present equilibrium and non-equilibrium self-assembly approaches to the synthetic construction of discrete hybrid (inorganic-organic) nano-objects and higher-level nanostructured networks. We examine a range of synthetic modalities under equilibrium conditions that give rise to integrative self-assembly (supramolecular wrapping, nanoscale incarceration and nanostructure templating) or higher-order self-assembly (programmed/directed aggregation). We contrast these strategies with processes of transformative self-assembly that use self-organizing media, reaction-diffusion systems and coupled mesophases to produce higher-level hybrid structures under non-equilibrium conditions. Key elements of the constructional codes associated with these processes are identified with regard to existing theoretical knowledge, and presented as a heuristic guideline for the rational design of hybrid nano-objects and nanomaterials.
了解化学衍生过程如何在扩展的多个长度尺度上控制物质的构建和组织,在材料研究的许多领域中越来越受到关注。在这里,我们回顾了目前用于合成离散杂化(无机-有机)纳米物体和更高层次纳米结构网络的平衡和非平衡自组装方法。我们研究了一系列在平衡条件下产生整合自组装(超分子包裹、纳米级包封和纳米结构模板化)或高阶自组装(编程/定向聚集)的合成方式。我们将这些策略与转化自组装过程进行对比,后者利用自组织介质、反应扩散系统和耦合中间相在非平衡条件下产生更高层次的杂化结构。根据现有的理论知识,确定了与这些过程相关的构建代码的关键要素,并将其作为合理设计杂化纳米物体和纳米材料的启发式指南呈现出来。