Radical-Involved Photosynthesis of AuCN Oligomers from Au Nanoparticles and Acetonitrile

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• 作者：Renhong Li ; Hisayoshi Kobayashi ; Jiawei Tong ; Xiaoqing Yan ; Yu Tang ; Shihui Zou ; Jiabin Jin ; Wuzhong Yi ; Jie Fan
• 刊名：The Journal of the American Chemical Society
• 出版年：2012
• 出版时间：November 7, 2012
• 年：2012
• 卷：134
• 期：44
• 页码：18286-18294
• 全文大小：613K
• 年卷期：v.134,no.44(November 7, 2012)
• ISSN：1520-5126

文摘

We show here the first radical route for the direct photosynthesis of AuCN oligomers with different sizes and shapes, as evidenced by TEM observations, from an Au nanoparticle/benzaldehyde/CH₃CN ternary system in air under UV-light irradiation. This photochemical route is green, mild, and universal, which makes itself distinguishable from the common cyanidation process. Several elementary reaction steps, including the strong C鈥揅 bond dissociation of CH₃CN and subsequent 鈥N radical addition to Au, have been suggested to be critical in the formation of AuCN oligomers based on the identification of 鈥N radical by in situ EPR and the radical trapping technique, and other reaction products by GC-MS and ¹H NMR, and DFT calculations. The resulting solid-state AuCN oligomers exhibit unique spectroscopic characters that may be a result of the shorter Au鈥揂u distances (namely, aurophilicity) and/or special polymer-like structures as compared with gold cyanide derivatives in the aqueous phase. The nanosized AuCN oligomers supported on mesoporous silica showed relatively good catalytic activity on the homogeneous annulation of salicylaldehyde with phenylacetylene to afford isoflavanones employing PBu₃ as the cocatalyst under moderate conditions, which also serves as evidence for the successful production of AuCN oligomers.