Max Planck Institute for Solid State Research, 70569 Stuttgart, Germany.
National Institute of Materials Physics, Atomistilor 405A, 077125 Magurele, Ilfov, Romania.
J Phys Chem Lett. 2023 Mar 2;14(8):2072-2077. doi: 10.1021/acs.jpclett.2c03575. Epub 2023 Feb 17.
The changes of properties and preferential interactions based on subtle energetic differences are important characteristics of organic molecules, particularly for their functionalities in biological systems. Only slightly energetically favored interactions are important for the molecular adsorption and bonding to surfaces, which define their properties for further technological applications. Here, prochiral tetracenothiophene molecules are adsorbed on the Cu(111) surface. The chiral adsorption configurations are determined by Scanning Tunneling Microscopy studies and confirmed by first-principles calculations. Remarkably, the selection of the adsorption sites by chemically different moieties of the molecules is dictated by the arrangement of the atoms in the first and second surface layers. Furthermore, we have investigated the thermal effects on the direct desulfurization reaction that occurs under the catalytic activity of the Cu substrate. This reaction leads to a product that is covalently bound to the surface in chiral configurations.
基于细微能量差异的性质变化和优先相互作用是有机分子的重要特征,特别是对它们在生物系统中的功能而言。只有略微有利的相互作用对于分子在表面的吸附和键合很重要,这决定了它们在进一步技术应用中的性质。在这里,前手性四并噻吩分子被吸附在 Cu(111)表面上。手性吸附构型通过扫描隧道显微镜研究确定,并通过第一性原理计算得到证实。值得注意的是,分子化学性质不同的部分对吸附位点的选择取决于第一层和第二层原子的排列。此外,我们还研究了在 Cu 基底的催化活性下发生的直接脱硫反应的热效应。该反应导致产物以手性构型与表面共价结合。