4.8 Article

Molecular-Scale Ligand Effects in Small Gold-Thiolate Nanoclusters

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 140, 期 45, 页码 15430-15436

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jacs.8b09440

关键词

-

资金

  1. NSERC CGS-Alexander Graham Bell scholarship
  2. NSERC
  3. U.S. Department of Energy (DOE)
  4. NSERC Canada
  5. University of Washington
  6. DOE [DE-AC02-06CH11357]
  7. Canadian Light Source (CLS)
  8. APS
  9. Air Force Office of Scientific Research under AFOSR Award [FA9550-15-1-9999 (FA9550-15-1-0154)]
  10. Ministry of Education, Singapore [R-279-000-481-112]
  11. Spanish Ministry of Economy and Competitiveness (MINECO) [CTQ2017-85496-P]
  12. Agencia de Gestio d'Ajuts Universitaris i de Recerca (AGAUR) [SGR2017-1189]

向作者/读者索取更多资源

Because of the small size and large surface area of thiolate-protected Au nanoclusters (NCs), the protecting ligands are expected to play a substantial role in modulating the structure and properties, particularly in the solution phase. However, little is known on how thiolate ligands explicitly modulate the structural properties of the NCs at atomic level, even though this information is critical for predicting the performance of Au NCs in application settings including as a catalyst interacting with small molecules and as a sensor interacting with biomolecular systems. Here, we report a combined experimental and theoretical study, using synchrotron X-ray spectroscopy and quantum mechanics/molecular mechanics simulations, that investigates how the protecting ligands impact the structure and properties of small Au-18(SR)(14) NCs. Two representative ligand types, smaller aliphatic cyclohexanethiolate and larger hydrophilic glutathione, are selected, and their structures are followed experimentally in both solid and solution phases. It was found that cyclohexanethiolate ligands are significantly perturbed by toluene solvent molecules, resulting in structural changes that cause disorder on the surface of Au-18(SR)(14) NCs. In particular, large surface cavities in the ligand shell are created by interactions between toluene and cyclohexanethiolate. The appearance of these small molecule-accessible sites on the NC surface demonstrates the ability of Au NCs to act as a catalyst for organic phase reactions. In contrast, glutathione ligands encapsulate the Au NC core via intermolecular interactions, minimizing structural changes caused by interactions with water molecules. The much better protection from glutathione ligands imparts a rigidified surface and ligand structure, making the NCs desirable for biomedical applications due to the high stability and also offering a structural-based explanation for the enhanced photoluminescence often reported for glutathione-protected Au NCs.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据