纳米颗粒
X射线光电子能谱
胶体金
化学
药物化学
立体化学
组合化学
纳米技术
物理
材料科学
核磁共振
作者
Adam J. Young,Markus Sauer,Guilherme M. D. M. Rúbio,Akiko Satô,Annette Foelske,Christopher J. Serpell,Jia Min Chin,Michael R. Reithofer
出处
期刊:Nanoscale
[Royal Society of Chemistry]
日期:2019-01-01
卷期号:11 (17): 8327-8333
被引量:79
摘要
Although N-heterocyclic carbenes (NHCs) have been demonstrated as suitable ligands for the stabilisation of gold nanoparticles (AuNPs) through a variety of methods, the manner in which such AuNPs form is yet to be fully elucidated. We report a simple and fast one-step synthesis of uniform chiral (l/d)-histidin-2-ylidene stabilised gold nanoparticles using the organometallic Au(i) complex as a well defined starting material. The resulting nanoparticles have an average size of 2.35 ± 0.43 nm for the L analog whereas an average size of 2.25 ± 0.39 nm was found for the D analog. X-ray photoelectron spectroscopy analyses reveal the presence of Au(i) and Au(0) in all NHC stabilised AuNPs. In contrast, measured X-ray photoelectron spectra of dodecanethiol protected gold nanoparticles showed only the presence of a Au(0) species. This observation leads us to postulate that AuNPs synthesised from organometallic NHC-Au(i) complexes exhibit a monolayer of Au(i) surrounding a Au(0) core. This work highlights the importance of synthetic method choice for NHC-stabilized AuNPs, as this could determine Au oxidation states and resulting AuNP properties such as catalytic activities and stabilities.
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