Ji Penghui, Dettmann Dominik, Liu Ying-Hsuan, Berti Giulia, Preetha Genesh Navathej, Cui Daling, MacLean Oliver, Perepichka Dmytro F, Chi Lifeng, Rosei Federico
Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices, Institute of Functional Nano & Soft Materials, Soochow University, Suzhou 215123, China.
Centre Énergie, Matériaux et Télécommunications, Institut National de la Recherche Scientifique, 1650 Boulevard Lionel-Boulet, Varennes, Québec J3X 1P7, Canada.
ACS Nano. 2022 Apr 26;16(4):6506-6514. doi: 10.1021/acsnano.2c00831. Epub 2022 Apr 1.
Surface-confined reactions represent a powerful approach for the precise synthesis of low-dimensional organic materials. A complete understanding of the pathways of surface reactions would enable the rational synthesis of a wide range of molecules and polymers. Here, we report different reaction pathways of tetrathienylbenzene (T1TB) and its extended congener tetrakis(dithienyl)benzene (T2TB) on Cu(111), investigated using scanning tunneling microscopy, X-ray photoelectron spectroscopy, and density functional theory calculations. Both T1TB and T2TB undergo desulfurization when deposited on Cu(111) at room temperature. Deposition of T1TB at 453 K yields pentacene through desulfurization, hydrogen transfer, and a cascade of intramolecular cyclization. In contrast, for T2TB the intramolecular cyclization stops at anthracene and the following intermolecular C-C coupling produces a conjugated ladder polymer. We show that tandem desulfurization/C-C coupling provides a versatile approach for growing carbon-based nanostructures on metal surfaces.
表面受限反应是精确合成低维有机材料的一种有效方法。全面了解表面反应途径将有助于合理合成各种分子和聚合物。在此,我们报告了四噻吩基苯(T1TB)及其扩展同系物四(二噻吩基)苯(T2TB)在Cu(111)上的不同反应途径,采用扫描隧道显微镜、X射线光电子能谱和密度泛函理论计算进行了研究。T1TB和T2TB在室温下沉积在Cu(111)上时都会发生脱硫反应。在453 K下沉积T1TB通过脱硫、氢转移和一系列分子内环化反应生成并五苯。相比之下,对于T2TB,分子内环化反应在蒽处停止,随后的分子间C-C偶联产生一种共轭梯形聚合物。我们表明,串联脱硫/C-C偶联为在金属表面生长碳基纳米结构提供了一种通用方法。