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超壬苯并菲的表面合成与表征

On-Surface Synthesis and Characterization of Super-nonazethrene.

作者信息

Turco Elia, Mishra Shantanu, Melidonie Jason, Eimre Kristjan, Obermann Sebastian, Pignedoli Carlo A, Fasel Roman, Feng Xinliang, Ruffieux Pascal

机构信息

nanotech@surfaces laboratory, Empa - Swiss Federal Laboratories for Materials Science and Technology, 8600 Dübendorf, Switzerland.

Faculty of Chemistry and Food Chemistry, and Center for Advancing Electronics Dresden, Technical University of Dresden, 01069 Dresden, Germany.

出版信息

J Phys Chem Lett. 2021 Sep 2;12(34):8314-8319. doi: 10.1021/acs.jpclett.1c02381. Epub 2021 Aug 24.

Abstract

Beginning with the early work of Clar et al. in 1955, zethrenes and their laterally extended homologues, super-zethrenes, have been intensively studied in the solution phase and widely investigated as optical and charge transport materials. Superzethrenes are also considered to exhibit an open-shell ground state and may thus serve as model compounds to investigate nanoscale π-magnetism. However, their synthesis is extremely challenging due to their high reactivity. We report here the on-surface synthesis of the hitherto largest zethrene homologue-super-nonazethrene-on Au(111). Using single-molecule scanning tunneling microscopy and spectroscopy, we show that super-nonazethrene exhibits an open-shell singlet ground state featuring a large spin polarization-driven electronic gap of 1 eV. Consistent with the emergence of an open-shell ground state, high-resolution tunneling spectroscopy reveals singlet-triplet spin excitations in super-nonazethrene, characterized by a strong intramolecular magnetic exchange coupling of 51 meV. Given the paucity of zethrene chemistry on surfaces, our results therefore provide unprecedented access to large, open-shell zethrene compounds amenable to scanning probe measurements, with potential application in molecular spintronics.

摘要

从1955年克拉尔等人的早期工作开始,泽特烯及其横向扩展的同系物——超级泽特烯,就在溶液相中得到了深入研究,并作为光学和电荷传输材料受到广泛关注。超级泽特烯也被认为呈现开壳基态,因此可作为研究纳米级π磁性的模型化合物。然而,由于其高反应活性,它们的合成极具挑战性。我们在此报告在金(111)表面上迄今最大的泽特烯同系物——超级九氮杂并五苯的表面合成。利用单分子扫描隧道显微镜和光谱学,我们表明超级九氮杂并五苯呈现开壳单重基态,其特征是由大的自旋极化驱动的1电子伏特的电子能隙。与开壳基态的出现相一致,高分辨率隧道光谱揭示了超级九氮杂并五苯中的单重态-三重态自旋激发,其特征是有51毫电子伏特的强分子内磁交换耦合。鉴于表面上泽特烯化学研究的匮乏,我们的结果因此为适用于扫描探针测量的大型开壳泽特烯化合物提供了前所未有的研究途径,在分子自旋电子学中具有潜在应用。

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