化学
齿合度
胶体金
催化作用
热重分析
纳米颗粒
透射电子显微镜
X射线光电子能谱
组合化学
高分子化学
核磁共振波谱
配体(生物化学)
光谱学
质子核磁共振
金属有机化学
立体化学
选择性催化还原
结晶学
有机化学
对映选择合成
红外光谱学
作者
Sophie R. Thomas,Tristan Tsai Yuan Tan,Guilherme M. D. M. Rúbio,Monnaya Chalermnon,Jia Min Chin,Michael R. Reithofer
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2025-09-12
卷期号:64 (38): 19316-19324
被引量:1
标识
DOI:10.1021/acs.inorgchem.5c03050
摘要
A series of gold nanoparticles (AuNPs) stabilized by bidentate acyclic diamino carbenes (ADCs) were synthesized via the reduction of dimeric gold(I) complexes. The resulting ADC-AuNPs were characterized by NMR spectroscopy, UV-vis spectroscopy, X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), and thermogravimetric analysis (TGA), revealing nanoparticles with a narrow size distribution and sizes ranging from 1.7 to 3.3 nm. This synthetic approach was extended to an asymmetric dinuclear ADC-gold(I) complex, affording slightly larger AuNPs (∼4 nm) upon reduction. The ADC-AuNPs with shorter linkers exhibited significant catalytic activity for the reduction of 4-nitrophenol, demonstrating a versatile and efficient route to catalytically active gold nanoparticles stabilized by both symmetric and asymmetric ADC ligands.
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