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ChemCatChem · 2013 ·Vol. 5 ·期 12 ·3788-3793 · IF 5.181

Silicon Nanowire Arrays – A New Catalyst for the Reduction of Nitrobenzene Derivatives

Yajun Xu,Lei Wang,Wenwen Jiang,Hongwei Wang,Jianlin Yao,Qinghua Guo,Lin Yuan,Hong Chen

Graphical No need to be noble: Hydrogen fluoride-treated silicon nanowire arrays (H-SiNWAs) are an efficient, recyclable catalyst for the chemical reduction of nitrobenzene derivatives. The activity of H-SiNWAs is because of the presence of Si  H bonds and the length of the nanowires. Silicon nanowire arrays (SiNWAs) are under extensive investigation for solar cells and biomedical applications. This study reports for the first time that hydrogen fluoride-treated (H)-SiNWAs are an efficient catalyst for the reduction of nitrobenzene derivatives. We show that SiNWAs, after hydrogen fluoride treatment, have a high catalytic activity in p -nitrophenol (PNP) reduction. The conversion rate of PNP by H-SiNWAs increases with time and is almost complete within 30 min, which thus indicates catalytic activity comparable to that of platinum nanoparticles. The catalytic activity of SiNWAs is closely related to the chemical composition and specific morphology of the surface. Si  H bonds on the surface are essential for activity, and arrays with longer nanowires showed a higher catalytic activity. Moreover, the activity can be easily regenerated by hydrogen fluoride treatment. It was also found that H-SiNWAs exhibit a similar catalytic activity for the reduction of other nitrobenzene derivatives such as p -nitroaniline and sodium m -nitrobenzenesulfonate. It is concluded that H-SiNWAs may be considered as an environmentally friendly alternative to noble-metal-based catalysts for the reduction of nitrobenzene derivatives.

CAS / MDL: 100-02-7 16940-66-2
研究领域: 材料科学 · 化学工程 · 环境科学
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MOLECULES · 2023 ·Vol. 28 ·期 10 ·4082 · IF 4.6

Visible Light-Mediated Organoboron-Catalyzed Metal-Free Synthesis of Silanols from Silanes

Jinbo Yang,Xiangxue Cao,Lanfeng Wei,Jianshu Zhang,Jinli Zhang,Ping Liu,Liang Xu,Pengfei Li

Herein, a four-coordinated organoboron compound, aminoquinoline diarylboron (AQDAB), is utilized as the photocatalyst in the oxidation of silane to silanol. This strategy effectively oxidizes Si–H bonds, affording Si–O bonds. Generally, the corresponding silanols can be obtained in moderate to good yields at room temperature under oxygen atmospheres, representing a green protocol to complement the existing preparation methods for silanols.Keywords:photocatalytic oxidation;silane;silanol;aminoquinoline diarylboron

研究领域: 有机化学 · 光化学 · 催化 · 绿色化学
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