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衬底诱导的构象变化和分子组装:β-取代寡聚噻吩在 Au(111)表面吸附单层的原位 STM 观察。

Substrate-induced varied conformation and molecular assemblies: in situ STM observation of beta-substituted oligothiophene adlayers on Au(111).

机构信息

Department of Applied Chemistry, Graduate School of Engineering, Tohoku University, Aoba-yama 04, Sendai 980-8579, Japan.

出版信息

Langmuir. 2010 May 18;26(10):7148-52. doi: 10.1021/la9042183.

Abstract

The adsorption of 3,3'''-dihexyl-2,2':5',2'':5'',2'''-quaterthiophene (4T) molecules on an Au(111) electrode was examined by using in situ scanning tunneling microscopy in 0.10 M HClO(4), revealing internal molecular structures of the tetrathiophene backbones and the hexyl side chains. The 4T admolecules were packed in lamellae with their molecular axis aligned along the main axis of the Au(111) substrate and their hexyl side chains interdigitated to enhance intermolecular interaction. Dynamics of molecular organization incurred by the shifting of potential was also observed in this study. By examining and comparing the adsorption of 4T on HOPG and Au(111), we address the role of the substrate in understanding the arrangement of 4T admolecules.

摘要

采用原位扫描隧道显微镜技术在 0.10 M HClO4 中研究了 3,3'''-二己基-2,2':5',2'':5'',2'''-四噻吩(4T)分子在 Au(111)电极上的吸附,揭示了四噻吩骨架和己基侧链的分子内结构。4T 吸附分子以其分子轴沿 Au(111)基底的主轴排列的层状排列,其己基侧链交错排列以增强分子间相互作用。在这项研究中还观察到了由电位移动引起的分子组织动力学。通过检查和比较 4T 在 HOPG 和 Au(111)上的吸附,我们解决了底物在理解 4T 吸附分子排列中的作用。

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