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金纳米粒子的胺端烷硫醇功能化的 X 射线光电子能谱表征。

X-ray photoelectron spectroscopy characterization of gold nanoparticles functionalized with amine-terminated alkanethiols.

机构信息

National ESCA and Surface Analysis Center for Biomedical Problems, Departments of Chemical Engineering and Bioengineering, University of Washington Box, Seattle, USA.

出版信息

Biointerphases. 2011 Sep;6(3):98. doi: 10.1116/1.3622481.

Abstract

Gold nanoparticles (AuNPs) functionalized with a short chain amine-terminated alkanethiol (HS-(CH(2))(2)NH(2) or C2 NH(2)-thiol) are prepared via a direct synthesis method and then ligand-exchanged with a long chain amine-terminated alkanethiol (HS-(CH(2))(11)NH(2) or C11 NH(2)-thiol). Transmission electron microscopy analysis showed the AuNPs were relatively spherical with a median diameter of 24.2 ± 4.3 nm. X-ray photoelectron spectroscopy was used to determine surface chemistry of the functionalized and purified AuNPs. The ligand-exchange process was monitored within the time range from 30 min to 61 days. By the fourth day of exchange all the C2 NH(2)-thiol molecules had been replaced by C11 NH(2)-thiol molecules. C11 NH(2)-thiol molecules continued to be incorporated into the C11 NH(2) self-assembled monolayer between days 4 and 14 of ligand-exchange. As the length of the exchange time increased, the functionalized AuNPs became more stable against aggregation. The samples were purified by a centrifugation and resuspension method. The C2 NH(2) covered AuNPs aggregated immediately when purification was attempted. The C11 NH(2) covered AuNPs could be purified with minimal or no aggregation. Small amounts of unbound thiol (∼15%) and oxidized sulfur (∼20%) species were detected on the ligand-exchanged AuNPs. Some of the unbound thiol and all of the oxidized sulfur could be removed by treating the functionalized AuNPs with HCl.

摘要

金纳米粒子(AuNPs)通过直接合成方法功能化短链胺端烷硫醇(HS-(CH(2))(2)NH(2)或 C2 NH(2)-硫醇),然后与长链胺端烷硫醇(HS-(CH(2))(11)NH(2)或 C11 NH(2)-硫醇)进行配体交换。透射电子显微镜分析表明,AuNPs 具有相对球形的形状,平均直径为 24.2±4.3nm。X 射线光电子能谱用于确定功能化和纯化的 AuNPs 的表面化学。在 30 分钟至 61 天的时间范围内监测配体交换过程。到交换的第四天,所有 C2 NH(2)-硫醇分子都已被 C11 NH(2)-硫醇分子取代。在配体交换的第 4 天至第 14 天之间,C11 NH(2)-硫醇分子继续掺入 C11 NH(2)自组装单层中。随着交换时间的延长,功能化的 AuNPs 对聚集变得更加稳定。通过离心和再悬浮方法对样品进行纯化。当尝试进行纯化时,C2 NH(2)覆盖的 AuNPs 立即聚集。C11 NH(2)覆盖的 AuNPs 可以进行纯化,几乎没有或没有聚集。在配体交换的 AuNPs 上检测到少量未结合的硫醇(约 15%)和氧化硫(约 20%)物质。通过用 HCl 处理功能化的 AuNPs,可以去除一些未结合的硫醇和所有的氧化硫。

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