ISM, UMR CNRS N°5255, Univ. Bordeaux, 33405 Talence, France.
UMR 6226, Institut des Sciences Chimiques de Rennes, CNRS-Université de Rennes 1, Campus de Beaulieu, 35042 Rennes, France.
Nat Commun. 2016 Oct 19;7:13152. doi: 10.1038/ncomms13152.
Understanding the relationship between the location of nanoparticles (NPs) in an organic matrix and their catalytic performances is essential for catalyst design. Here we show that catalytic activities of Au, Ag and CuNPs stabilized by dendrimers using coordination to intradendritic triazoles, galvanic replacement or stabilization outside dendrimers strongly depends on their location. AgNPs are found at the inner click dendrimer periphery, whereas CuNPs and AuNPs are encapsulated in click dendrimer nanosnakes. AuNPs and AgNPs formed by galvanic replacement are larger than precursors and only partly encapsulated. AuNPs are all the better 4-nitrophenol reduction catalysts as they are less sterically inhibited by the dendrimer interior, whereas on the contrary CuNPs are all the better alkyne azide cycloaddition catalysts as they are better protected from aerobic oxidation inside dendrimers. This work highlights the role of the location in macromolecules on the catalytic efficiency of metal nanoparticles and rationalizes optimization in catalyst engineering.
了解纳米粒子(NPs)在有机基质中的位置与其催化性能之间的关系对于催化剂设计至关重要。在这里,我们表明,使用三唑与树枝状大分子内部配位、电置换或在树枝状大分子外部稳定的 Au、Ag 和 CuNPs 的催化活性强烈取决于它们的位置。AgNPs 位于点击树枝状大分子的内部外围,而 CuNPs 和 AuNPs 则被包裹在点击树枝状大分子纳米蛇中。通过电置换形成的 AuNPs 和 AgNPs 比前体大,且只有部分被包裹。AuNPs 是更好的 4-硝基苯酚还原催化剂,因为它们受到树枝状大分子内部的空间位阻抑制较小,而相反,CuNPs 是更好的炔烃叠氮化物环加成催化剂,因为它们在树枝状大分子内部更好地受到有氧氧化的保护。这项工作强调了大分子中位置对金属纳米粒子催化效率的作用,并合理化了催化剂工程中的优化。