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Molecular Modulator Approach for Controlling the Length of Chiral 1D Single-Helical Gold Nanoparticle Superstructures

机译:控制手性一维单螺旋金纳米颗粒超结构长度的分子调制剂方法

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摘要

Peptide-based methods have proven useful for constructing helical gold nanoparticle superstructures that exhibit strong plasmonic chiroptical activity. Superstructure syntheses using the amphiphilic peptide conjugate CI6-(AYSSGAPP-M°*PPF)2 typically yield ID helices with a broad length distribution. In this study,we introduce a molecular modulator approach for controlling helix length. It represents a first step toward achieving narrowly disperse populations of single helices fabricated using peptide-based methods. Varying amounts of modulator,C16-(AYSSGA)2,were added to C16-(AYSSGAPP-McxPPF)2-based single-helix syntheses,resulting in decreased helix length and narrowing of the helix length distribution. Kinetic studies of fiber assembly were performed to investigate the mechanism by which the modulator affects helix length. It was found that the modulator leads to rapid peptide conjugate nucleation and fiber growth,which in turn results in large amounts of short fibers that serve as the underlying scaffold for the single-helix superstructures. These results constitute important advances toward generating monodisperse samples of plasmonic helical colloids.
机译:基于肽的方法已被证明可用于构建具有强等离子体手性活性的螺旋金纳米颗粒超结构。使用两亲性肽偶联物CI6-(AYSSGAPP-M°*PPF)2合成的上层结构通常产生具有较宽长度分布的ID螺旋。在这项研究中,我们引入了一种控制螺旋长度的分子调节剂方法。它代表了使用基于肽的方法实现窄分散的单个螺旋群体的第一步。在基于C16-(AYSSGAPP-McxPPF)2的单螺旋合成中加入不同量的调制剂C16-(AYSSGA)2,导致螺旋长度减小,螺旋长度分布变窄。对纤维组装进行了动力学研究,研究了调制器影响螺旋长度的机理。研究发现,调节剂导致肽共轭成核和纤维生长的快速,进而产生大量的短纤维,作为单螺旋超结构的底层支架。这些结果为生成等离子体螺旋胶体的单分散样品提供了重要进展。

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