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单分子分辨率的表面支撑的乌尔曼偶联反应中的有机金属中间体。

Single-molecule resolution of an organometallic intermediate in a surface-supported Ullmann coupling reaction.

机构信息

Department of Physics, The Hong Kong University of Science and Technology, Hong Kong, China.

出版信息

J Am Chem Soc. 2011 Aug 31;133(34):13264-7. doi: 10.1021/ja204956b. Epub 2011 Jul 21.

Abstract

We have studied the organometallic intermediate of a surface-supported Ullmann coupling reaction from 4, 4″-dibromo-p-terphenyl to poly(para-phenylene) by scanning tunneling microscopy/spectroscopy and density functional theory calculations. Our study reveals at a single-molecular level that the intermediate consists of biradical terphenyl (ph)(3) units that are connected by single Cu atoms through C-Cu-C bridges. Upon further increasing the temperature, the neighboring biradical (ph)(3) units are coupled by C-C bonds forming poly(para-phenylene) oligomers while the Cu atoms are released.

摘要

我们通过扫描隧道显微镜/光谱和密度泛函理论计算研究了 4,4″-二溴-对三联苯到聚对亚苯基的表面支撑 Ullmann 偶联反应的有机金属中间体。我们的研究在单分子水平上揭示了该中间体由双自由基三联苯(ph)(3)单元组成,这些单元通过 Cu-C-C 桥连接到单个 Cu 原子上。进一步提高温度时,相邻的双自由基(ph)(3)单元通过 C-C 键连接形成聚对亚苯基低聚物,同时释放出 Cu 原子。

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