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Multifunctional behavior of molecules comprising stacked cytosine–AgI–cytosine base pairs; towards conducting and photoluminescence silver-DNA nanowires

机译:包含堆积的胞嘧啶-AgI-胞嘧啶碱基对的分子的多功能行为;走向导电和光致发光银-DNA纳米线

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摘要

DNA molecules containing a 1D silver array may be applied for nanotechnology applications, but first their conducting and photoluminescence behavior must be enhanced. Here we have synthesized and characterized three new helical compounds based on stacked silver–mediated cytosine base pairs [Ag(mC)2]X (mC = N1-methylcytosine; X = NO3 (>1), BF4 (>2) and ClO4 (>3)), that contain uninterrupted polymeric AgI chains that run through the center of the helixes, comparable to related silver-DNA structures. The exposure of nanostructures of [Ag(mC)2]BF4 (>2) to cold hydrogen plasma stimulates the reduction of the prearranged AgI polymeric chains to metallic silver along the material. This solvent-free reduction strategy leads to the compound [AgI(mC)2]X@Ag0 (>2H) that contains uniformly well-distributed silver metallic nanostructures that are responsible for the new conducting and photoluminescence properties of the material. The presence of silver nanostructures alongside compound >2H has been evaluated by means of X-ray photoelectron spectroscopy (XPS), UV-vis spectroscopy, and X-ray powder diffraction (XRPD). The conducting and photoactive properties of >2H were studied by electrostatic force microscopy (EFM) and conducting-AFM (c-AFM), and photoluminescence microscopy (PL), respectively. The results demonstrate that the presence of well-organized metallic silver nanoentities on the material is responsible for the novel conductivity and photoactive properties of the material. This methodology can be employed for the generation of multifunctional silver-DNA related materials with tailored properties.
机译:包含一维银阵列的DNA分子可以用于纳米技术,但是首先必须增强其导电和光致发光性能。在这里,我们基于堆积的银介导的胞嘧啶碱基对[Ag(mC)2] X(mC = N1-甲基胞嘧啶; X = NO3(> 1 ),BF4( > 2 )和ClO4(> 3 )),它们包含贯穿螺旋中心的不间断聚合Ag I 链,与相关的银相当-DNA结构。 [Ag(mC)2] BF4(> 2 )的纳米结构暴露于冷氢等离子体中会刺激沿着材料将预先排列的Ag I 聚合物链还原为金属银。这种无溶剂的还原策略导致化合物[Ag I (mC)2] X @ Ag 0 (> 2H )均匀地包含-分布的银金属纳米结构,负责材料的新导电和光致发光性能。通过X射线光电子能谱(XPS),紫外可见光谱和X射线粉末衍射(XRPD)评估了银纳米结构与化合物> 2H 的存在。分别通过静电力显微镜(EFM)和导电AFM(c-AFM)和光致发光显微镜(PL)研究了> 2H 的导电和光活性性质。结果表明,材料上组织良好的金属银纳米实体是材料的新型导电性和光敏性能的原因。该方法可用于生成具有定制特性的多功能银-DNA相关材料。

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