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Surface Supported Gold-Organic Hybrids: On-Surface Synthesis and Surface Directed OrientationSurface Supported Gold-Organic Hybrids: On-Surface Synthesis and Surface Directed Orientation

机译:表面支撑的金有机杂化物:表面合成和表面定向取向表面支撑的金有机杂化物:表面合成和表面定向取向

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摘要

The surface-assisted synthesis of gold-organic hybrids on Au (111) and Au (100) surfaces is reported by thermally initiated dehalogenation of chloro-substituted perylene-3,4,9,10-tetracarboxylic acid bisimides (PBIs). Structures and surface-directed alignment of the Au-PBI chains are investigated by scanning tunnelling microscopy in ultrahigh vacuum conditions. Using dichloro-PBI as a model system, the mechanism for the formation of Au-PBI dimer is revealed with scanning tunnelling microscopy studies and density functional theory calculations. A PBI radical generated from the homolytic C一Cl bond dissociation can covalently bind a surface gold atom and partially pull it out of the surface to form stable PBI-Au hybrid species,which also gives rise to the surface-directed alignment of the Au-PBI chains on reconstructed Au (100) surfaces.
机译:通过热取代氯代per-3,4,9,10-四羧酸双酰亚胺(PBIs)引发的脱卤作用,报道了Au(111)和Au(100)表面上金-有机杂化物的表面辅助合成。 Au-PBI链的结构和表面定向排列是通过扫描隧道显微镜在超高真空条件下进行的。使用二氯-PBI作为模型系统,通过扫描隧道显微镜研究和密度泛函理论计算揭示了Au-PBI二聚体形成的机理。由均相C一Cl键解离产生的PBI自由基可以共价结合表面金原子,并将其部分拉出表面,形成稳定的PBI-Au杂种,这也导致Au-的表面定向排列重建的Au(100)表面上的PBI链。

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