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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Light-Responsive Polymer Surfaces via Postpolymerization Modification of Grafted Polymer-Brush Structures
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Light-Responsive Polymer Surfaces via Postpolymerization Modification of Grafted Polymer-Brush Structures

机译:通过接枝聚合物-毛刷结构的后聚合改性获得光响应性聚合物表面

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摘要

Light-induced, spatially well-defined, reversible switching of surface properties enables the creation of remote-controlled smart surfaces. We have taken advantage of the unique high-resolution structuring capabilities of extreme ultraviolet (EUV) interference lithography to produce nanostructured photoresponsive polymer brushes. Patterns of poly(glycidyl methacrylate) (PGMA) and poly(methacrylic acid) (PMAA) were grafted from two different 100 mu m thick fluoropolymer substrates by means of a radiation-initiated, grafting-from approach based on free-radical polymerization (FRP). Photochromic properties were introduced via novel one- or two-step postpolymerization modifications with spiropyran (SP) derivatives, which allowed us to control the number of photochromic groups on the polymer brushes. Depending on the degree of functionalization and the local chemical environment, the SP moieties can open upon UV-light exposure to form zwitterionic, deeply colored, and fluorescent merocyanines (MCs) and reclose to the colorless SP configuration via thermal or visible light-induced relaxation. Switching kinetics were studied by means of time-resolved fluorescence microscopy and compared with kinetic measurements of the SP moiety in solution. The results indicated the importance, for the intensity of the switching, of the local chemical environment provided by both the polymer brush and added solvents, and showed the predominant influence on the ring-closing kinetics of polar solvents, which stabilize the MC form. To allow further characterization of the polymer-brush arrangements on a macroscopic scale, similar, but unstructured brush systems were grafted from fluoropolymers after large-area activation using EUV radiation or argon plasma. All steps of the postpolymerization modification were characterized in detail using attenuated total reflection infrared (ATR-IR) spectroscopy. Furthermore, a light-induced reversible static-contact-angle switch with a range of up to 15 degrees for PGMA-SP brushes and up to 30 degrees for PMA-SP brushes was demonstrated upon alternating UV- and visible-light irradiation.
机译:光诱导的,空间上明确定义的,可逆的表面特性切换可创建远程控制的智能表面。我们利用了极紫外(EUV)干涉光刻技术独特的高分辨率结构化能力来生产纳米结构的光敏聚合物刷。通过基于自由基聚合(FRP)的辐射引发接枝方法,从两种不同的100微米厚的含氟聚合物基材上接枝了聚甲基丙烯酸缩水甘油酯(PGMA)和聚甲基丙烯酸(PMAA)的图案。 )。通过使用螺吡喃(SP)衍生物进行新型的一步或两步后聚合修饰,引入了光致变色特性,这使我们能够控制聚合物刷上的光致变色基团的数量。取决于功能化程度和局部化学环境,SP部分可在紫外线照射下打开以形成两性离子,深色和荧光性花青素(MC),并通过热或可见光引起的弛豫重新接近无色SP构型。通过时间分辨荧光显微镜研究转换动力学,并将其与溶液中SP部分的动力学测量结果进行比较。结果表明,对于转换强度而言,由聚合物刷和添加的溶剂共同提供的局部化学环境非常重要,并且显示了对稳定MC形式的极性溶剂的闭环动力学的主要影响。为了在宏观尺度上进一步表征聚合物刷的布置,在使用EUV辐射或氩等离子体进行大面积活化之后,从含氟聚合物中接枝了类似但非结构化的刷系统。使用衰减全反射红外(ATR-IR)光谱详细描述了聚合后修饰的所有步骤。此外,在交替的紫外线和可见光照射下,展示了一种光感应可逆静态接触角开关,对于PGMA-SP刷子,其最大范围为15度,对于PMA-SP刷子,其最大范围为30度。

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