首页> 美国卫生研究院文献>Scientific Reports >Ullmann Coupling Reactions on Ag(111) and Ag(110); Substrate Influence on the Formation of Covalently Coupled Products and Intermediate Metal-Organic Structures
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Ullmann Coupling Reactions on Ag(111) and Ag(110); Substrate Influence on the Formation of Covalently Coupled Products and Intermediate Metal-Organic Structures

机译:Ag(111)和Ag(110)的Ullmann偶联反应;基质对共价偶联产物和中间金属有机结构形成的影响

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摘要

On-surface reactions based on Ullmann coupling are known to proceed on coinage-metal substrates (e.g. Au, Ag, Cu), with the chemistry of the surface strongly influencing the reaction progression. In addition, the topography of the surface may be expected to affect the local adsorption geometry of the reactants as well as the intermediate and final structures. Here, we investigate the effect of two different surface facets of silver, Ag(111) and Ag(110) on the formation of organometallic and covalent structures for Ullmann-type coupling reactions. Deposition of 4,4”-diiodo-m-terphenyl molecules onto either Ag(111) or Ag(110) surfaces leads to the scission of C-I bonds followed by the formation of organometallic zigzag structures, consisting of molecules connected by coordination bonds to Ag adatoms. The covalently coupled product is formed by annealing each surface, leading to the removal of Ag atoms and the formation of covalently bonded zigzag poly(m-phenylene) structures. Comparisons of the adsorption model of molecules on each surface before and after annealing reveal that on Ag(111), structures rearrange by rotation and elongation of bonds in order to become commensurate with the surface, whereas for the Ag(110) surface, the similarity in adsorption geometry of the intermediate and final states means that no rotation is required.
机译:已知基于Ullmann偶联的表面反应在造币金属基材(例如Au,Ag,Cu)上进行,并且表面化学性质强烈影响反应进程。另外,可以预期表面的形貌会影响反应物以及中间结构和最终结构的局部吸附几何形状。在这里,我们调查的两个不同的银,Ag(111)和Ag(110)的不同表面刻面对形成有机金属和共价结构的Ullmann型偶联反应的影响。在Ag(111)或Ag(110)表面上沉积4,4”-二碘-间-三联苯分子会导致CI键断裂,随后形成有机金属之字形结构,该结构由通过配位键连接至Ag的分子组成原子通过退火每个表面形成共价偶联的产物,从而导致Ag原子的去除和共价键合的锯齿形聚间亚苯基结构的形成。退火前后每个表面上分子的吸附模型的比较表明,在Ag(111)上,结构通过旋转和键的延伸而重新排列,以使其与表面相称,而对于Ag(110)表面,相似性处于中间态和最终态的吸附几何形状意味着不需要旋转。

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