Gerencia de Química, Comisión Nacional de Energía Atómica, Argentina.
Langmuir. 2010 Apr 20;26(8):5559-67. doi: 10.1021/la9038304.
A robust and straightforward strategy allowing the controlled confinement of metal nanoparticles within the 3D framework of mesoporous films is presented. The chemical methodology is based on the inner surface modification of mesoporous silica films with polyelectrolyte brushes. We demonstrate that the macromolecular building blocks significantly enhance the site-selective preconcentration of nanoparticle precursors in the inner environment of the mesoporous film. Then, chemical reduction of the preconcentrated precursors led to the formation of metal nanoparticles locally addressed in the mesoporous structure. We show that the synergy taking place between two versatile functional nanobuilding blocks (ordered mesocavities and polymer brushes) can produce stable embedded nanoparticles with tuned optical properties in a very simple manner. As a general framework, the strategy can be easily adapted to different sets of polymer brushes and mesoporous films in order to regulate the monomer-precursor interactions and, consequently, manipulate the site-selective character of the different chemistries taking place in the film. We consider that the "integrative chemistry" approach described in this work provides new pathways to manipulate the physicochemical characteristics of hybrid organic-inorganic advanced functional assemblies based on the rational design of chemistry and topology in confined environments.
提出了一种稳健而直接的策略,可将金属纳米粒子在介孔薄膜的 3D 框架内进行受控限制。该化学方法基于通过聚电解质刷对内表面改性介孔硅薄膜。我们证明了这些大分子构建基块极大地增强了纳米颗粒前体在介孔薄膜的内环境中的选择性预浓缩。然后,通过化学还原预浓缩的前体导致金属纳米颗粒在介孔结构中局部形成。我们表明,两个多功能纳米构建基块(有序介孔腔和聚合物刷)之间发生的协同作用可以以非常简单的方式产生具有可调光学性质的稳定嵌入式纳米颗粒。作为一个通用框架,该策略可以很容易地适应不同的聚合物刷和介孔薄膜组,以调节单体-前体相互作用,从而控制在薄膜中发生的不同化学物质的选择性特征。我们认为,本文所述的“综合化学”方法为在受限环境中基于化学和拓扑结构的合理设计来操纵基于有机-无机杂化的先进功能组件的物理化学特性提供了新途径。