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表面乌尔曼聚合反应的实时成像揭示了吸附原子的抑制作用。

Real-Time Imaging of On-Surface Ullmann Polymerization Reveals an Inhibiting Effect of Adatoms.

作者信息

Dettmann Dominik, Panighel Mirco, Preetha Genesh Navathej, Galeotti Gianluca, MacLean Oliver, Farnesi Camellone Matteo, Johal Tarnjit Kaur, Fabris Stefano, Africh Cristina, Perepichka Dmytro F, Rosei Federico, Contini Giorgio

机构信息

Centre Énergie, Matériaux et Télécommunications, Institut National de la Recherche Scientifique Department, 1650 Boulevard Lionel-Boulet, Varennes, J3X 1P7 Québec, Canada.

Istituto di Struttura della Materia-CNR (ISM-CNR), Via Fosso del Cavaliere 100, 00133 Roma, Italy.

出版信息

J Am Chem Soc. 2024 Sep 4;146(35):24493-24502. doi: 10.1021/jacs.4c06994. Epub 2024 Aug 21.

Abstract

Ullmann coupling is a widely used reaction for the on-surface growth of low-dimensional carbon nanomaterials. The irreversible nature of this reaction prevents the "self-healing" of defects, and a detailed knowledge of its mechanism is therefore essential to enable the growth of extended ordered structures. However, the dynamics of the Ullmann polymerization remain largely unexplored, as coupling events occur on a timescale faster than conventional scanning probe microscopy imaging frequencies. Here, we reveal the dynamics of these surface events using high-speed variable-temperature scanning tunneling microscopy (STM) (10 frames per second). Performing the measurements at the onset reaction temperatures provides an unprecedented description of the evolution of organometallic (OM) and covalent surface species during the Ullmann polymerization of -dibromobenzene on Cu(110). Our results demonstrate the existence of an intermediate OM phase with Cu adatoms that inhibits the polymerization. These observations now complete the picture of the pathways of on-surface Ullmann polymerization, which includes the complex interplay of the phenylene moieties and metal atoms. Our work demonstrates the unique capability of high-speed STM to capture the dynamics of molecular self-assembly and coupling.

摘要

乌尔曼偶联反应是一种广泛应用于低维碳纳米材料表面生长的反应。该反应的不可逆性阻碍了缺陷的“自我修复”,因此,详细了解其反应机理对于实现扩展有序结构的生长至关重要。然而,乌尔曼聚合反应的动力学在很大程度上仍未得到探索,因为偶联事件发生的时间尺度比传统扫描探针显微镜成像频率更快。在这里,我们使用高速变温扫描隧道显微镜(STM)(每秒10帧)揭示了这些表面事件的动力学。在起始反应温度下进行测量,为在Cu(110)上对二溴苯进行乌尔曼聚合反应期间有机金属(OM)和共价表面物种的演变提供了前所未有的描述。我们的结果表明存在一种含有铜吸附原子的中间OM相,它会抑制聚合反应。这些观察结果现在完善了表面乌尔曼聚合反应途径的全貌,其中包括亚苯基部分和金属原子的复杂相互作用。我们的工作展示了高速STM捕捉分子自组装和偶联动力学的独特能力。

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