化学学报 ›› 2025, Vol. 83 ›› Issue (6): 563-568.DOI: 10.6023/A25030101 上一篇    下一篇

研究通讯

常温常压下金纳米线催化芳基炔烃与NaBH4的还原氢化反应

孙满鑫, 张卫, 姬梦圆, 张延华*()   

  1. 南京工业大学 化学与分子工程学院 南京 211816
  • 投稿日期:2025-03-31 发布日期:2025-05-09
  • 基金资助:
    南京工业大学科研启动基金(39837126)

Ambient Reductive Hydrogenation of Aryl Alkynes with NaBH4 Catalyzed by Gold Nanowires

Manxin Sun, Wei Zhang, Mengyuan Ji, Yanhua Zhang*()   

  1. School of Chemistry and Molecular Engineering, Nanjing Tech University, Nanjing 211816, China
  • Received:2025-03-31 Published:2025-05-09
  • Contact: *E-mail: ias_yhzhang@njtech.edu.cn
  • Supported by:
    Start-up Fund from Nanjing Tech University(39837126)

本工作所报道的芳基炔烃在常温常压下的还原氢化反应, 关键在于使用了硼氢化钠(NaBH4)作为还原剂和金纳米线(AuNWs)作为催化剂. 在AuNWs的用量仅为0.76 mol%的条件下, 芳基炔烃可成功被NaBH4还原, 反应4 h后总产率可达92%, 其主要产物为半氢化烯烃产物. 这一方法推进了芳基炔烃在温和条件下的还原反应研究, 同时为AuNWs材料在有机合成领域的应用开辟了新的途径.

关键词: 常温常压, 芳基炔烃, 还原氢化, 金纳米线, 硼氢化钠

The traditional reductive hydrogenation of alkynes usually requires the use of suitable catalysts with high activity, sometimes under harsh reaction conditions like high temperature and high pressure. To improve the reaction efficiency, various catalysts have been developed, such as metallic, nonmetallic, metal-organic frameworks and porous materials, etc. Especially, the efficient catalysts that can catalyze the hydrogenation of alkynes under mild reaction conditions have attracted increasing attention. In recent years, with the rapid development of nanotechnology, more and more nanomaterials have been successfully applied in conventional organic reactions as catalysts, achieving exciting results. Gold nanomaterials are one of the typical metal nanomaterials. Their synthesis and application have always been a hot topic. Gold nanowires (AuNWs) are a unique class of one-dimensional nanostructures with large specific surface areas and multiple active sites, thus exhibiting excellent catalytic efficiency. In this work, AuNWs are applied to the hydrogenation of aryl alkynes with sodium borohydride (NaBH4) at ambient conditions. The results indicate that C≡C bonds on alkynes are reduced to C=C and C—C smoothly. Here, AuNWs with different length are synthesized by using 1,3,5-triethynylbenzene as the ligand, which effectively reduces the adverse effects of competitive adsorption of ligand and substrate in subsequent catalytic reactions. The reductive hydrogenation was firstly investigated with 4-ethynylbiphenyl (17.8 mg, 0.1 mmol) as the model substrate. The results indicated that the reduction products, including olefins and alkanes, were successfully obtained with AuNWs (0.76 mol%) as the catalyst and NaBH4 (2 equiv.) as the reducing agent in 1.5 mL of ethyl acetate solvent. By high performance liquid chromatography (HPLC) analysis, the overall yield of products is determined to be 92% after 4 h of reaction, and the molar ratio of olefins to alkanes is 72∶28. Furthermore, it is noted that the proportion of alkanes increases with the reaction time and surpasses olefins after 12.5 h of reaction. It means that the selectivity of the hydrogenation of alkynes can be adjusted to a certain extent by reaction time. The reaction is applicable to various aryl alkyne substrates, including mono-alkynes, poly-alkynes, heteroaryl alkynes and internal alkynes. In conclusion, AuNWs exhibit high catalytic activity in the reductive hydrogenation of aryl alkynes, thus achieving the transformation under mild reaction conditions. It can be foreseen that AuNWs will have more excellent performances in organic catalysis due to their unique properties.

Key words: ambient condition, aryl alkyne, reductive hydrogenation, gold nanowires, sodium borohydride