Mawélé Loudy Coste, Allouche Joachim, Bousquet Antoine, Martinez Hervé, Billon Laurent
Universite de Pau et Pays de l'Adour, E2S UPPA, CNRS, Institut des Sciences Analytiques & de Physico-Chimie pour l'Environnement & les Matériaux, UMR5254, 64000, Pau, France.
Nanoscale. 2020 Apr 14;12(14):7532-7537. doi: 10.1039/c9nr10740a. Epub 2020 Mar 27.
Herein, we report the selective functionalization of nano-domains obtained by the self-assembly of a polystyrene-block-poly(vinyl benzyl azide) PS-b-PVBN copolymer synthesized in three steps. First, a polystyrene macro-initiator was synthesized, and then extended with vinyl benzyl chloride by nitroxide mediated polymerization to form polystyrene-block-poly(vinyl benzyl chloride) PS-b-PVBC. Nucleophilic substitution of vinyl benzyl chloride into a vinyl benzyl azide moiety is finally performed to obtain PS-b-PVBN which self-assembled into nano-domains of vinyl benzyl azide PVBN. Click chemistry was then used to bind functional gold nanoparticles and poly(N-isopropylacrylamide) (PNIPAM) on PVBN domains due to the specific anchoring at the surface of the nanopatterned film. Atomic force microscopy (AFM) was used to observe the block copolymer self-assembly and the alignment of the gold nanoparticles at the surface of the PVBN nanodomains. Thorough X-ray photoelectron spectroscopy (XPS) analysis of the functional film showed evidence of the sequential grafting of nanoparticles and PNIPAM. The hybrid surface expresses thermo-responsive properties and serves as a pattern to perfectly align and control the assembly of inorganic particles at the nanoscale.
在此,我们报道了通过三步合成的聚苯乙烯-嵌段-聚(乙烯基苄基叠氮)PS-b-PVBN共聚物自组装获得的纳米域的选择性功能化。首先,合成聚苯乙烯大分子引发剂,然后通过氮氧自由基介导的聚合反应与乙烯基苄基氯反应,形成聚苯乙烯-嵌段-聚(乙烯基苄基氯)PS-b-PVBC。最后将乙烯基苄基氯进行亲核取代反应生成乙烯基苄基叠氮部分,从而得到PS-b-PVBN,其自组装成乙烯基苄基叠氮PVBN的纳米域。由于在纳米图案化薄膜表面的特异性锚定作用,随后利用点击化学将功能性金纳米颗粒和聚(N-异丙基丙烯酰胺)(PNIPAM)结合到PVBN域上。利用原子力显微镜(AFM)观察嵌段共聚物的自组装以及金纳米颗粒在PVBN纳米域表面的排列情况。对功能薄膜进行全面的X射线光电子能谱(XPS)分析,结果表明纳米颗粒和PNIPAM存在顺序接枝的证据。这种杂化表面具有热响应特性,并作为一种图案在纳米尺度上完美地排列和控制无机颗粒的组装。