Judd Chris J, Junqueira Filipe L Q, Haddow Sarah L, Champness Neil R, Duncan David A, Jones Robert G, Saywell Alex
School of Physics & Astronomy, The University of Nottingham, Nottingham, NG7 2RD, UK.
School of Chemistry, The University of Nottingham, Nottingham, NG7 2RD, UK.
Commun Chem. 2020 Nov 11;3(1):166. doi: 10.1038/s42004-020-00402-0.
The on-surface synthesis of covalently bonded materials differs from solution-phase synthesis in several respects. The transition from a three-dimensional reaction volume to quasi-two-dimensional confinement, as is the case for on-surface synthesis, has the potential to facilitate alternative reaction pathways to those available in solution. Ullmann-type reactions, where the surface plays a role in the coupling of aryl-halide functionalised species, has been shown to facilitate extended one- and two-dimensional structures. Here we employ a combination of scanning tunnelling microscopy (STM), X-ray photoelectron spectroscopy (XPS) and X-ray standing wave (XSW) analysis to perform a chemical and structural characterisation of the Ullmann-type coupling of two iodine functionalised species on a Ag(111) surface held under ultra-high vacuum (UHV) conditions. Our results allow characterisation of molecular conformations and adsorption geometries within an on-surface reaction and provide insight into the incorporation of metal adatoms within the intermediate structures of the reaction.
共价键合材料的表面合成在几个方面与溶液相合成不同。从三维反应体积转变为准二维受限环境,就像表面合成那样,有可能促进形成与溶液中不同的反应路径。乌尔曼型反应中,表面在芳基卤化物官能化物种的偶联中发挥作用,已被证明有助于形成扩展的一维和二维结构。在此,我们结合扫描隧道显微镜(STM)、X射线光电子能谱(XPS)和X射线驻波(XSW)分析,对在超高真空(UHV)条件下保持在Ag(111)表面上的两种碘官能化物种的乌尔曼型偶联进行化学和结构表征。我们的结果能够表征表面反应中的分子构象和吸附几何结构,并深入了解金属吸附原子在反应中间结构中的掺入情况。