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Hyperbranched polymer-gold nanoparticle assemblies : role of polymer architecture in hybrid assembly formation and SERS activity

机译:超支化聚合物-金纳米颗粒组件:聚合物体系结构在混合组件形成和SERS活性中的作用

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摘要

Plasmonic gold nano-assemblies that self-assemble with the aid of linking molecules or polymers have the potential to yield controlled hierarchies of morphologies and consequently result in materials with tailored optical (e.g. localized surface plasmon resonances (LSPR)) and spectroscopic properties (e.g. surface enhanced Raman scattering (SERS)). Molecular linkers that are structurally well-defined are promising for forming hybrid nano-assemblies which are stable in aqueous solution and are increasingly finding application in nanomedicine. Despite much ongoing research in this field, the precise role of molecular linkers in governing the morphology and properties of the hybrid nano-assemblies remains unclear. Previously we have demonstrated that branched linkers, such as hyperbranched polymers, with specific anchoring end groups can be successfully employed to form assemblies of gold NPs demonstrating near-infrared SPRs and intense SERS scattering. We herein introduce a tailored polymer as a versatile molecular linker, capable of manipulating nano-assembly morphologies and hot-spot density. In addition, this report explores the role of the polymeric linker architecture, specifically the degree of branching of the tailored polymer in determining the formation, morphology and properties of the hybrid nano-assemblies. The degree of branching of the linker polymer, in addition to the concentration and number of anchoring groups, is observed to strongly influence the self-assembly process. The assembly morphology shifts primarily from 1D-like chains to 2D plates and finally to 3D-like globular structures, with increase in degree of branching. Insights have been gained into how the morphology influences the SERS performance of these nano-assemblies with respect to hot-spot density. These findings supplement the understanding of the morphology determining nano-assembly formation and pave the way for the possible application of these nano-assemblies as SERS bio-sensors for medical diagnostics.
机译:借助连接分子或聚合物自组装的等离子金纳米组件有可能产生可控的形态层次,因此导致材料具有定制的光学(例如局部表面等离振子共振(LSPR))和光谱特性(例如表面)增强拉曼散射(SERS))。在结构上明确定义的分子接头有望用于形成在水溶液中稳定的杂化纳米组装件,并越来越多地在纳米医学中得到应用。尽管在该领域进行了大量的研究,但是分子连接子在控制杂化纳米组件的形态和性能方面的确切作用仍不清楚。先前我们已经证明,具有特定锚定端基的支化接头(例如超支化聚合物)可以成功地用于形成金NP的组装体,从而证明了近红外SPR和强烈的SERS散射。我们在本文中介绍了一种定制的聚合物,它是一种通用的分子接头,能够操纵纳米组装体的形态和热点密度。此外,本报告探讨了聚合物接头结构的作用,特别是定制聚合物在确定杂化纳米组件的形成,形态和性能方面的支化程度。观察到,除了锚固基团的浓度和数量以外,连接基聚合物的支化程度还强烈影响自组装过程。随着分支程度的增加,组装形态主要从一维状链转变为二维板,最后转变为3D状球状结构。已经获得了关于形态如何影响这些纳米组件在热点密度方面的SERS性能的见解。这些发现补充了对确定纳米组件形成的形态学的理解,并为将这些纳米组件用作医学诊断的SERS生物传感器铺平了道路。

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