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将单壁碳纳米管特异性固定到单链和一维 DNA 折纸结构上。

Site-specific immobilization of single-walled carbon nanotubes onto single and one-dimensional DNA origami.

机构信息

Department of Chemistry, Marshall University, Huntington, West Virginia 25755, USA.

出版信息

J Am Chem Soc. 2013 Feb 20;135(7):2451-4. doi: 10.1021/ja312191a. Epub 2013 Feb 8.

Abstract

Development of a simple and efficient methodology to control the placement, spacing, and alignment of single-walled carbon nanotubes (SWCNTs) is essential for nanotechnology device application. Building on the growing understanding that the strong π-π interaction between the bases of single-stranded DNA (ssDNA) and CNTs is sufficient not only to drive CNT solubility in water but also to stabilize individual nanotubes against clustering in aqueous solution, a new motif for functionalizing DNA origami (DO) with CNTs is demonstrated. CNTs solubilized via wrapping with ssDNA react with DO constructs displaying linear arrays of ssDNA, leading to immobilization of the CNTs onto the DO scaffold. This study demonstrates the immobilization of ssDNA-wrapped CNTs at specific positions on single DO constructs. Furthermore, multiple DO constructs assembled into extended one-dimensional arrays have been used to successfully align pairs of CNTs exceeding 500 nm in length in a parallel orientation. This result provides a simplified, alternative approach to immobilization of CNTs with programmed spacing and orientation.

摘要

开发一种简单高效的方法来控制单壁碳纳米管(SWCNTs)的放置、间距和排列对于纳米技术器件的应用至关重要。越来越多的研究表明,单链 DNA(ssDNA)碱基与 CNT 之间的强π-π相互作用不仅足以驱动 CNT 在水中的溶解度,而且足以稳定单个 CNT 以防其在水溶液中聚集。本文展示了一种用 CNT 功能化 DNA 折纸(DO)的新方案。通过 ssDNA 包裹而溶解的 CNT 与显示线性 ssDNA 阵列的 DO 结构发生反应,导致 CNT 固定在 DO 支架上。本研究证明了 ssDNA 包裹的 CNT 可以固定在单个 DO 结构上的特定位置。此外,已将多个 DO 结构组装成扩展的一维阵列,成功地将长度超过 500nm 的对 CNT 以平行取向对齐。该结果提供了一种简化的替代方法,用于固定具有编程间距和取向的 CNT。

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