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银表面的取向驱动均偶联反应中的反应活性和选择性。

The Orientation of Silver Surfaces Drives the Reactivity and the Selectivity in Homo-Coupling Reactions.

作者信息

Kalashnyk Nataliya, Salomon Eric, Mun Sung Hwan, Jung Jaehoon, Giovanelli Luca, Angot Thierry, Dumur Frédéric, Gigmes Didier, Clair Sylvain

机构信息

Aix Marseille Univ, Univ Toulon, CNRS, IM2NP, Marseille, France.

Aix Marseille Univ, CNRS, PIIM, Marseille, France.

出版信息

Chemphyschem. 2018 May 6. doi: 10.1002/cphc.201800406.

DOI:10.1002/cphc.201800406
PMID:29732680
Abstract

Original reaction pathways can be explored in the on-surface synthesis approach where small aromatic precursors are confined to the surface of single crystal metals. The bis-indanedione molecule reacted with itself on silver surfaces in different ways, through a Knoevenagel reaction or an oxidative coupling, leading to the formation of a variety of new molecular compounds and covalently-linked 1D or 2D networks. Noteworthy, original reaction products were obtained that cannot be synthesized in traditional solvent-based chemistry. The lowest activation temperature for the homo-coupling reactions was found on the Ag(111) surface. The Ag(110) was highly selective in terms of coupling reaction type, while on Ag(100) the temperature could finely control the selectivity. The on-surface synthesis approach is shown here to be particularly efficient to produce original compounds in mild conditions, using activation temperatures as low as 200 °C. The different structures were characterized by scanning tunnelling microscopy (STM) together with X-ray photoelectron emission spectroscopy (XPS) and high-resolution electron energy loss spectroscopy (HREELS).

摘要

在表面合成方法中可以探索原始反应途径,在该方法中,小的芳香族前体被限制在单晶金属表面。双茚二酮分子在银表面以不同方式进行自身反应,通过克诺文纳格尔反应或氧化偶联,导致形成各种新的分子化合物以及共价连接的一维或二维网络。值得注意的是,获得了在传统的基于溶剂的化学中无法合成的原始反应产物。在Ag(111)表面发现了均偶联反应的最低活化温度。Ag(110)在偶联反应类型方面具有高度选择性,而在Ag(100)上,温度可以精细地控制选择性。本文表明,表面合成方法在温和条件下使用低至200 °C的活化温度来制备原始化合物时特别有效。通过扫描隧道显微镜(STM)以及X射线光电子发射光谱(XPS)和高分辨率电子能量损失光谱(HREELS)对不同结构进行了表征。

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